Search Result

Results for "

cluster of differentiation 47 (CD47)

" in MedChemExpress (MCE) Product Catalog:

By Targets:	CD3 (1) CD47 (40) FLT3 (2) Nuclear Factor of activated T Cells (NFAT) (1) 5 alpha Reductase (1) 5-HT Receptor (9) AAK1 (2) ADAMTS (1) ADC Antibody (2) ADC Linker (1) ADC Payload (1) Adhesion G Protein-coupled Receptors (AGPCRs) (1) Adrenergic Receptor (4) Akt (3) Amino Acid Derivatives (1) Amyloid-β (2) Androgen Receptor (1) Angiotensin-converting Enzyme (ACE) (2) Antibiotic (4) Antibody-Drug Conjugates (ADCs) (1) Antifolate (1) Apoptosis (35) Autophagy (4) Bacterial (17) Bcl-2 Family (3) Bcr-Abl (4) BCRP (1) Biochemical Assay Reagents (43) Btk (2) c-Kit (1) c-Met/HGFR (1) c-Myc (2) Cannabinoid Receptor (1) Caspase (5) Cathepsin (1) CCR (1) CD19 (1) CD28 (2) CD73 (1) CDK (10) CGRP Receptor (2) Cholinesterase (ChE) (9) COX (1) Cuproptosis (2) CXCR (1) Cyclic GMP-AMP Synthase (1) Cytochrome P450 (2) Dihydrofolate reductase (DHFR) (2) DNA Alkylator/Crosslinker (1) DNA/RNA Synthesis (3) Dopamine Receptor (2) Drug Derivative (8) Drug Intermediate (3) Drug Isomer (5) Drug Metabolite (17) Drug-Linker Conjugates for ADC (2) EGFR (6) Endogenous Metabolite (31) Epigenetic Reader Domain (2) ERK (3) Estrogen Receptor/ERR (4) FAAH (1) Ferroptosis (3) FGFR (1) Flavivirus (4) Fluorescent Dye (11) Fungal (5) G-quadruplex (1) GABA Receptor (2) GCGR (1) GHSR (1) Glutathione Peroxidase (2) Glutathione S-transferase (1) Glycosidase (1) GPR55 (2) GSK-3 (1) HBV (1) HCV (1) HDAC (4) HIF/HIF Prolyl-Hydroxylase (4) Histamine Receptor (1) Histone Demethylase (1) Histone Methyltransferase (5) HIV (6) HIV Protease (2) HSP (3) Huntingtin (1) IAP (1) iGluR (2) IKK (2) IKZF Family (1) Influenza Virus (1) Insecticide (4) Interleukin Related (11) Isotope-Labeled Compounds (28) JAK (1) JNK (2) Kallikrein (2) Keap1-Nrf2 (2) Kinesin (1) Ligands for Target Protein for PROTAC (2) Liposome (9) Lipoxygenase (1) LPL Receptor (2) mAChR (1) MDM-2/p53 (1) MEK (1) Microtubule/Tubulin (4) Mitochondrial Metabolism (3) Mitosis (1) MMP (3) Monoamine Oxidase (6) mTOR (2) Na+/K+ ATPase (2) NAMPT (2) Necroptosis (1) Neurokinin Receptor (4) Neurotensin Receptor (1) NF-κB (10) NO Synthase (1) NOD-like Receptor (NLR) (1) OAT (1) P2Y Receptor (2) p38 MAPK (4) PAK (1) Parasite (8) PARP (1) PD-1/PD-L1 (6) Phosphatase (2) Phosphodiesterase (PDE) (1) Phospholipase (2) Phosphomannose Isomerase (PMI) (1) Polo-like Kinase (PLK) (1) Potassium Channel (1) PPAR (1) Prostaglandin Receptor (3) PROTACs (5) Proteasome (1) PTEN (1) Radionuclide-Drug Conjugates (RDCs) (1) Raf (1) RANKL/RANK (1) Ras (2) Reactive Oxygen Species (ROS) (11) Reference Standards (19) Renin (1) RET (1) RGS Protein (1) ROCK (1) ROR (2) ROS Kinase (1) SARS-CoV (5) Ser/Thr Protease (4) Serotonin Transporter (1) Sigma Receptor (1) Small Interfering RNA (siRNA) (4) Smo (1) Sodium Channel (2) SOS1 (2) STAT (4) STING (7) Tau Protein (2) TGF-beta/Smad (2) TGF-β Receptor (6) Thyroid Hormone Receptor (2) TNF Receptor (11) Toll-like Receptor (TLR) (1) Topoisomerase (1) Transferrin Receptor (1) Transmembrane Glycoprotein (6) TROP2 (2) TRP Channel (3) Tryptophan Hydroxylase (1) Tyrosinase (3) VD/VDR (9) VEGFR (1) Virus Protease (2) Wnt (1) Xanthine Oxidase (1) Zinc Finger Protein (1)
By Research Areas:	Cancer (194) Cardiovascular Disease (19) Endocrinology (15) Infection (61) Inflammation/Immunology (87) Metabolic Disease (49) Neurological Disease (70)
Click Chemistry:	Alkynes (4)
Oligonucleotides:	Solvents (1) Nucleotides and their Analogs (2) A (3) Nucleosides and their Analogs (2) U (1) Aptamers (1) Rat Pre-designed siRNA Sets (1) Mouse Pre-designed siRNA Sets (1) Cationic Lipids (4) Human Pre-designed siRNA Sets (1) siRNAs (4)

501

Inhibitors & Agonists

Screening Libraries

Fluorescent Dye

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

Natural
Products

222

Recombinant Proteins

Isotope-Labeled Compounds

265

Antibodies

Click Chemistry

Oligonucleotides

Targets Recommended: CD47 CD3 CD6 CD2 Neprilysin FLT3 Anaplastic lymphoma kinase (ALK) P-glycoprotein Nuclear Factor of activated T Cells (NFAT)

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-P990131

*Anti-Mouse CD47/IAP Antibody (MIAP301)* 1 Publications Verification	CD47	Infection Inflammation/Immunology Cancer
Anti-Mouse CD47/IAP Antibody (MIAP301) is an anti-mouse *CD47/IAP* IgG2a monoclonal antibody. Anti-Mouse CD47/IAP Antibody (MIAP301) can effectively block CD47 signaling and enhance macrophage phagocytic function. Anti-Mouse CD47/IAP Antibody (MIAP301) can increase the infiltration of immune cells. Anti-Mouse CD47/IAP Antibody (MIAP301) restores the phagocytic function of myeloid cells and alleviate B cell inhibition. Anti-Mouse CD47/IAP Antibody (MIAP301) may interfere with wound healing. Anti-Mouse CD47/IAP Antibody (MIAP301) can be used for research on cancer, inflammation and infection conditions such as melanoma, intestinal mucosal repair and sepsis .

HY-P990132

*Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410)*	CD47	Inflammation/Immunology Cancer
Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) is an anti-mouse/rat/human *CD47/IAP* IgG1 monoclonal antibody. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can effectively block CD47 signaling and enhance macrophage phagocytic function. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can increase the infiltration of immune cells. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) may interfere with wound healing. Anti-Mouse/Rat/Human CD47/IAP Antibody (MIAP410) can be used for research on cancer and inflammation conditions such as breast cancer and intestinal mucosal repair .

HY-P99172

CC-90002	CD47 Interleukin Related	Cancer
CC-90002 is a *humanized anti-CD47* monoclonal antibody (mAb)*. CC-90002 has a high affinity for binding to CD47* with a subnanomolar K_d value. CC-90002 can be used for the research of hematologic malignancies and solid tumors .

HY-P990858

*Anti-CD47* Antibody (B6.H12)**	CD47	Cancer
Anti-CD47 Antibody (B6.H12) is a kind of mouse IgG1 κ chimeric antibody, targeting to human *CD47. Anti-CD47* Antibody (B6.H12) blocks CD47 interactions with SIRPα. Anti-CD47 Antibody (B6.H12) inhibits cell proliferation, cell migration and invasion. Anti-CD47 Antibody (B6.H12) increases macrophage phagocytosis. Anti-CD47 Antibody (B6.H12) shows potent anti-tumor effect in various tumor models, such as osteosarcoma .

HY-P99533

Urabrelimab SRF-231; SRF231	CD47 Interleukin Related	Cancer
Urabrelimab (SRF231) is a fully human anti-CD47 monoclonal antibody that blocks the CD47-SIRP interaction .

HY-RS02250

CD47 Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA) CD47	Others
CD47 Human Pre-designed siRNA Set A contains three designed siRNAs for CD47 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

CD47 Human Pre-designed siRNA Set A CD47 Human Pre-designed siRNA Set A

HY-RS16548

Cd47 Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Cd47 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cd47 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cd47 Mouse Pre-designed siRNA Set A Cd47 Mouse Pre-designed siRNA Set A

HY-RS22981

Cd47 Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
Cd47 Rat Pre-designed siRNA Set A contains three designed siRNAs for Cd47 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

Cd47 Rat Pre-designed siRNA Set A Cd47 Rat Pre-designed siRNA Set A

HY-P991085

HX009	PD-1/PD-L1	Cancer
HX009 is a bispecific antibody targeting PD1 and *CD47, but with weakened CD47* binding. HX009 blocks the functional of PD1/CD47. HX009 can be used for the study of non-Hodgkin’s lymphoma (NHL) .

HY-P991518

IBI-322	PD-1/PD-L1 CD47	Cancer
IBI-322 is a bispecific antibody targeting PD-L1 and *CD47. IBI-322 attenuates CD47* activity in monovalent binding and blockes PD-L1 activity in bivalent binding. IBI-322 selectively binds to CD47+PD-L1+ tumor cells, effectively inhibits CD47-SIRPα signal and triggered strong tumor cell phagocytosis in vitro .

HY-143224

NCGC00138783	CD47	Cancer
NCGC00138783 is a selective inhibitor targeting CD47/SIRPα axis, with an IC₅₀ of 50 µM. NCGC00138783 directly blocks the interaction between CD47 and SIRPα axis .

HY-143224B

NCGC00138783 TFA	CD47	Cancer
NCGC00138783 TFA is a selective inhibitor targeting CD47/SIRPα axis, with an IC₅₀ of 50 μM. NCGC00138783 TFA directly blocks the interaction between CD47 and SIRPα axis .

HY-115983

DMUP	CD47 Apoptosis	Cancer
DMUP is a potent CD47-SIRPα axis inhibitor. DMUP induces apoptosis and increases the macrophage phagocytosis in A549 cells. DMUP decreases the expression of CD47 and SIRPα protein. DMUP shows antitumor activity .

HY-143224A

NCGC00138783 free base	CD47	Cancer
NCGC00138783 free base is a selective inhibitor targeting CD47/SIRPα axis, with an IC₅₀ of 50 µM. NCGC00138783 free base directly blocks the interaction between CD47 and SIRPα axis .

HY-P990707

Maplirpacept TTI-622; PF-07901801	CD47	Inflammation/Immunology
Maplirpacept (TTI-622; PF-07901801) is a fusion protein consisting of the *CD47*-binding domain of human SIRPα linked to the Fc region of human IgG4. Maplirpacept enhances phagocytosis by blocking CD47 .

HY-P991062

Gentulizumab Gensci-059	CD47	Cancer
Gentulizumab (Gensci-059) is a humanized IgG4 antibody that targets *CD47. Gentulizumab displays strong binding to CD47* in both human and monkey, and effectively inhibits the CD47-SIRPα interaction. Gentulizumab exhibits a potent antitumor activity. The isotype control for Gentulizumab can refer to Human IgG4 (S228P) kappa, Isotype Control (HY-P99003) .

HY-P10813

ZLIRTLHEWY	CD47	Inflammation/Immunology Cancer
ZLIRTLHEWY is a potent peptide CD47/SIRPα interaction inhibitor. ZLIRTLHEWY is promising for research of cancers .

HY-P99950

Evorpacept ALX148	CD47	Cancer
Evorpacept is a high affinity *CD47*-blocking fusion protein with an inactive human immunoglobulin Fc region .

HY-P10420

RS17	CD47 Interleukin Related	Cancer
RS17 is an anti-tumor peptide designed to bind specifically to the *CD47* molecule and block the interaction between *CD47* and its ligand, SIRPα, on the surface membrane of macrophages. The main regulatory mechanism of RS17 is to prevent *CD47* from transmitting selective phagocytosis signals to SIRPα by binding to *CD47*, so that macrophages do not recognize tumor cells as their own tissue, but phagocytose them as foreign substances, thereby inhibiting immune escape of tumor cells. RS17 can be used to study the mechanism of anti-tumor response and immune escape .

HY-P99777

Ontorpacept TTI-621	CD47	Cancer
Ontorpacept (TTI-621) is a soluble fusion protein that consists of the human SIRPα N-terminal (1-118) linked to the Fc region of human IgG1. The N-terminal (1-118)-fragment of ontorpacept is a binding domain for CD47 which is an inhibitor of phagocytosis by macrophages. Ontorpacept is a *CD47-blocking* checkpoint inhibitor with antitumor activity .

HY-P990723

Timdarpacept	CD47	Cancer
Timdarpacept (DNL310) is a recombinant SIRPa-Fc fusion protein that can activate macrophages to enhance anti-tumor activity by blocking CD47-SIRPa .

HY-143225

NCGC00538431	CD47	Others
NCGC00538431 is a potent modulator of SIRPα-CD47 .

HY-P3968

Thrombospondin-1 (1016-1021) (human, bovine, mouse)	CD47	Others
Thrombospondin-1 (1016-1021) (human, bovine, mouse), a Thrombospondin-1-derived peptide, is a truncated peptide devoid of CD47-binding activity .

HY-P991016

Peluntamig PT-217	CD47	Inflammation/Immunology
HY-P991016 is an *CD47/DLL3*-targeting H-γ1_L-κ type bispecific antibody .

HY-P991560

TQB-2928	CD47	Cancer
TQB-2928 is a monoclonal antibody against *CD47*, which can be used in the study of cancer.

HY-P990694

Zeripatamig TG-1801	CD19 CD47	Inflammation/Immunology
Zeripatamig is an anti-CD19/CD47 human IgG1 κ monoclonal antibody . Recommend Isotype Controls: Human IgG1 kappa, Isotype Control (HY-P99001).

HY-P99029

Magrolimab 2 Publications Verification Hu5F9-G4	CD47	Cancer
Magrolimab (Hu5F9-G4) is a humanized anti-CD47 antibody. Magrolimab can block the "don't eat me" signal of *CD47*, thereby promoting macrophage mediated phagocytosis. Magrolimab has antitumor activity in malignant bone tumors and breast cancer .

HY-P991027

Spevatamig	CD47	Inflammation/Immunology
HY-P991027 is an *CD47/CLDN18*-targeting (H-γ1_L-κ)_(H-γ1_L-κ) type bispecific antibody .

HY-P991561

AO-176	CD47	Cancer
AO-176 is a humanized anti-CD47 IgG2 monoclonal antibody. AO-176 induces tumor phagocytosis through blocking the CD47-SIRPα interaction. AO-176 preferentially binds to tumor versus normal cells and directly kills tumor by a cell autonomous mechanism not ADCC (antibody-dependent cell-mediated cytotoxicity). AO-176 demonstrates dose-dependent antitumor activity in tumor xenograft models. AO-176 can be used for the researches of cancer, such as lymphoma .

HY-P991004

Itanistomig	CD47	Inflammation/Immunology
HY-P991004 is an *CD274/CD47*-targeting (VH-G1CH1-h)-H-γ1_L-κ-L-κ type bispecific antibody .

HY-P990954

Amulirafusp alfa	CD47	Inflammation/Immunology
HY-P990954 is an *MS4A1/CD47*-targeting IgG1κ type human antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001) .

HY-P990899

Amostomig	CD47	Inflammation/Immunology
HY-P990899 is an *CD274/CD47*-targeting IgG1λ2 type humanized antibody, the recommed isotype control is Human IgG1 lambda2, Isotype Control (HY-P990096) .

HY-P991023

Safimestomig	CD47	Inflammation/Immunology
HY-P991023 is an *CD47/CD274*-targeting IgG4κ type bispecific antibody, the recommed isotype control is Human IgG4 (S228P) kappa, Isotype Control (HY-P99003) .

HY-P99026

Lemzoparlimab TJ011133; TJC4	CD47	Cancer
Lemzoparlimab (TJ011133; TJC4) is a humanized anti-CD47 IgG4 antibody. Lemzoparlimab has a strong anti-tumor activity .

HY-P0144

Thrombospondin-1 (1016-1023) (human, bovine, mouse)	CD47 Apoptosis	Inflammation/Immunology
Thrombospondin-1 (1016-1023) (human, bovine, mouse), is the C-terminal end of the native sequence of Thrombospondin-1 (TSP-1), is a *CD47* agonist peptide .

HY-P99706

Ligufalimab AK 117	CD47 Interleukin Related	Cancer
Ligufalimab (AK 117) is a humanized IgG4 anti-CD47 monoclonal antibody. Ligufalimab does not induce RBC hemagglutination, and induces phagocytosis. Ligufalimab shows anti-tumor activity .

HY-151132

Glutaminyl cyclases-IN-1 IsoQC-IN-1	CD47	Cancer
Glutaminyl cyclases-IN-1 (IsoQC-IN-1) is a potent glutaminyl cyclases (QC) inhibitor with IC₅₀ values of 12 nM and 73 nM for human QC and isoQC, respectively. Glutaminyl cyclases-IN-1 can selectively interfere with the interaction of CD47/SIRPα through isoQC inhibition, and enhances the increased phagocytic activity of both THP-1 and U937 macrophages .

HY-P990962

Vislarafusp alfa	EGFR	Inflammation/Immunology
HY-P990962 is an *EGFR/CD47*-targeting IgG1κ type humanized antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001) .

HY-P10388

TAX2 peptide	CD47 TGF-β Receptor	Cancer
TAX2 peptide is a dodecapeptide based on molecular docking and simulation design, derived from the cell surface receptor CD47 sequence. TAX2 peptide acts as a selective antagonist of TSP-1 (thromboxin-1) interacting with CD47. TAX2 peptide can promote the binding of TSP-1 to CD36, which leads to the destruction of VEGFR2 (vascular endothelial growth factor receptor 2) activation, thereby blocking downstream NO (nitric oxide) signaling, demonstrating anti-angiogenic properties. TAX2 peptide can be used to study angiogenesis and tumor cell interactions in the tumor microenvironment .

HY-P990289

Anti-Mouse CD172a Antibody (P84)	Transmembrane Glycoprotein	Infection
Anti-Mouse CD172a Antibody (P84) is a rat-derived anti-mouse CD172a IgG1 κ type antibody inhibitor. Anti-Mouse CD172a Antibody (P84) blocks CD47-SIRPα interaction and thereby augments cell phagocytosis. Anti-Mouse CD172a Antibody (P84) can be used for the researches of infection and immunology, such as salmonella typhimurium infection .

HY-P99175

KWAR 23	CD47	Cancer
KWAR23 is an anti-human SIRPα antibody. KWAR23 binds human SIRPα with high affinity and disrupts its binding to CD47. KWAR23 shows antitumor activity in combination with tumor-opsonizing antibodies and can be used in cancer immunotherapy research .

HY-120284

CCCI-01	Microtubule/Tubulin	Cancer
CCCI-01 is a centrosome clustering inhibitor. CCCI-01 has selective effects on cancer. CCCI-01 can be used for the research of non-cross-resistant anti-cancer agents with blocking centrosome clustering .

HY-P3970

KRFK	TGF-β Receptor	Inflammation/Immunology
KRFK, a peptide derived from TSP-1, can activate TGF-β. KRFK promotes TGF-β-mediated signaling and its downstream role, independent of thrombospondin (TSP) receptors such as CD47 and CD36. KRFK can be used for chronic ocular surface inflammatory disorders reseach .

HY-P3970A

KRFK TFA 3 Publications Verification	TGF-β Receptor	Inflammation/Immunology
KRFK TFA, a peptide derived from TSP-1, can activate TGF-β. KRFK TFA promotes TGF-β-mediated signaling and its downstream role, independent of thrombospondin (TSP) receptors such as CD47 and CD36. KRFK TFA can be used for chronic ocular surface inflammatory disorders reseach .

HY-116681

Aflavarin	Insecticide	Infection
Aflavarin is produced from cluster 39 expressed mainly in sclerotia. Aflavarin exhibits anti-insectan activity .

HY-P991057

STI-6643	CD47	Cancer
STI-6643 is a fully human IgG4 antibody that targets *CD47*. STI-6643 displays potent anti-tumor activity with negligible RBC and lymphocyte toxicities. The isotype control for STI-6643 can refer to Human IgG4 (S228P) kappa, Isotype Control (HY-P99003) .

HY-136780

SEN177	Amyloid-β Apoptosis CD47 Huntingtin	Neurological Disease Cancer
SEN177 is an orally effect glutamine cyclase (QC) inhibitor. The K_i of SEN177 for human glutamine cyclase (hQC) is 20 nM, and the IC₅₀ is 13 nM. SEN177 interferes with the interaction between CD47 and SIRRPα, and has anti-tumor activity. SEN177 reduces aggregation and apoptosis caused by HTT mutation in Huntington model, and can be used in the study of neurodegenerative diseases .

HY-P990033

Anzurstobart CC-95251; BMS-986351	CD47	Cancer
Anzurstobart (CC-95251; BMS-986351) is a high-affinity, fully human monoclonal anti-SIRPα antibody that blocks the binding of CD47 to SIRPα. Anzurstobart enhances macrophage phagocytic activity against DLBCL cell lines in co-culture models when combined with the antibody Rituximab (HY-P9913). Anzurstobart has the potential for solid and hematologic malignancies research .

HY-16438

RRx-001 15+ Cited Publications Nibrozetone	CD47 Apoptosis Parasite	Infection Inflammation/Immunology Cancer
RRx-001, a hypoxia-selective epigenetic agent and studied as a radio- and chem-sensitizer, triggers apoptosis and overcomes agent resistance in myeloma. RRx-001 exhibits potent anti-tumor activity with minimal toxicity . RRx-001 is a dual small molecule checkpoint inhibitor by downregulating *CD47* and SIRP-α . RRx-001 is a potent inhibitor of G6PD and shows potent antimalarial activity .

HY-P99021

Galcanezumab 1 Publications Verification LY 2951742	CGRP Receptor	Neurological Disease
Galcanezumab (LY 2951742) is a humanized IgG4 monoclonal antibody against the CGRP ligand. Galcanezumab can be used for migraine or cluster headaches research .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-17409

Nystatin Maximum Cited Publications 40 Publications Verification	Infection Structural Classification Microorganisms Antifungal Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Mammalian Cell Culture Disease Research Disease Research Fields	Fungal Antibiotic Apoptosis Bacterial
Nystatin is an orally active polyene antifungal antibiotic effective against yeast and mycoplasma. Nystatin increases the permeability of plasma membranes to small monovalent ions, including chloridion . Nystatin is a cholesterol-sequestering agent , partially prevents Oxaliplatin-induced lipid raft aggregation, DR4 and DR5 clustering, and thereby reduces apoptosis .

HY-N6013

Aloin(mixture of A&B)	Infection Liliaceae Classification of Application Fields Ketones, Aldehydes, Acids Source classification Phenols Polyphenols Aloe vera (L.) Burm. f. Plants Inflammation/Immunology Disease Research Fields	MMP Bacterial Fungal
Aloin (mixture of A&B) is anthraquinone derivative isolated from Aloe vera. Aloin (mixture of A&B) has diverse biological activities such as anti-inflammatory, immunity, antidiabetic, antioxidant, antibacterial, antifungal, and antitumor activities. Aloin (mixture of A&B) also an effective inhibitor of stimulated granulocyte matrix metalloproteinases (MMPs) .

HY-W018772

D-Ribose(mixture of isomers) 3 Publications Verification	Structural Classification Microorganisms Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields Saccharides Cancer	Endogenous Metabolite
D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner .

HY-W018772R

D-Ribose(mixture of isomers) (Standard)	Structural Classification Microorganisms Source classification Endogenous metabolite Saccharides	Reference Standards Endogenous Metabolite
D-Ribose(mixture of isomers) (Standard) is the analytical standard of D-Ribose(mixture of isomers). This product is intended for research and analytical applications. D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner .

HY-P991518

IBI-322	Structural Classification Alkaloids Quinoline Alkaloids	PD-1/PD-L1 CD47
IBI-322 is a bispecific antibody targeting PD-L1 and *CD47. IBI-322 attenuates CD47* activity in monovalent binding and blockes PD-L1 activity in bivalent binding. IBI-322 selectively binds to CD47+PD-L1+ tumor cells, effectively inhibits CD47-SIRPα signal and triggered strong tumor cell phagocytosis in vitro .

HY-116681

Aflavarin	Structural Classification Microorganisms Source classification Coumarins Phenylpropanoids	Insecticide
Aflavarin is produced from cluster 39 expressed mainly in sclerotia. Aflavarin exhibits anti-insectan activity .

HY-121034

Acaterin	Structural Classification Natural Products Microorganisms Source classification	Bacterial
Acaterin is a compound isolated from Pseudomonas. Its biosynthetic gene cluster has been identified, and related studies have proposed its biosynthetic pathway. Comparative transcriptomics has shown that its formation is related to the bacterial regulatory network.

HY-149036

PAA5	Structural Classification Natural Products Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields Cancer	Ferroptosis Endogenous Metabolite Reactive Oxygen Species (ROS)
PAA5 is a methide carbon-centered polynuclear Au(I) cluster. PAA5 can release Au(I) causing Pro-oxidant response and accelerated ferroptosis. PAA5 increases the expression of pH2AX in a time-dependent manner. PAA5 has anticancer activity .

HY-131152

Leucinostatin (mixture of A&B)	Structural Classification Microorganisms Antifungal Classification of Application Fields Antibiotics Source classification Antibacterial Disease Research Anticancer Inflammation/Immunology Disease Research Fields Other Antibiotics	Antibiotic
Leucinostatin (mixture of A&B), the major components of an atypical nonapeptide complex produced by Paecilomyces lilacinus, are antibiotics .

HY-N12498

Aureonuclemycin	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Aureonuclemycin can be isolated from Staphylococcus aureus to obtain its biosynthetic gene cluster. Aureonuclemycin exists in two forms: Type A and Type B. Aureonuclemycin A is a nucleoside antibiotic that is structurally similar to herbicides and contains adenine. Aureonuclemycin B contains 5′-deoxyadenosine and exhibits antibacterial activity. Aureonuclemycin can be used in the research of bacterial leaf blight in rice, citrus canker, and bacterial leaf spot in rice. .

HY-150356MR1

Mixture of Aflatoxins in Acetonitrile (Standard)	Structural Classification Phenylpropanoids	Reference Standards
Mixture of Aflatoxins in Acetonitrile (Standard) is mainly used for the detection of aflatoxins in grain, oils, foods and traditional Chinese medicines

HY-N15691A

(E)-Tadehaginoside	Structural Classification Leguminosae Source classification Phenols Polyphenols Tadehagi triquetrum (L.) Ohashi Plants	Keap1-Nrf2 NF-κB
(E)-Tadehaginoside is the E-isomer of Tadehaginoside (HY-N15691). Tadehaginoside, a phenylpropanoid glycoside, is a regulator of lipogenesis and glucose consumption. Tadehaginoside has antioxygenic property. Tadehaginoside mediates liver protection against oxidative stress injury and inflammation by regulating Nrf2 and NF-κB signaling pathways in hepatocytes. Tadehaginoside can be used for the study of obesity and diabetes .

HY-W355141

Isopulegol	Structural Classification Natural Products Classification of Application Fields Source classification Myrtaceae Essence, Fragrance Cosmetic Research Plants Disease Research Fields Eucalyptus citriodora Hook. f. Cancer	Bacterial
Isopulegol is one of the main components of ECO (Eucalyptus citriodora oil). ECO has antibacterial activity .

HY-116757

(±)-α-CMBHC	Cardiovascular Disease Structural Classification Monophenols Classification of Application Fields Ketones, Aldehydes, Acids Source classification Phenols Endogenous metabolite Disease Research Fields	Endogenous Metabolite
(±)-α-CMBHC is a metabolite of α-Tocopherol .

HY-139637

(±)-Silybin Silibinin (mixture of Silybin A and Silybin B)	Structural Classification Flavanonols Flavonoids Source classification Cyamopsis tetragonoloba (L.) Taub. Plants Compositae	Apoptosis
(±)-Silybin is the racemate of Silybin (HY-N0779A). Silybin induces apoptosis and exhibits hepatoprotective, antioxidant, anti-inflammatory, anti-cancer activity .

HY-B1341

Norethynodrel Enidrel; SC 4642; NSC 15432	Structural Classification Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields Endocrinology Steroids	Endogenous Metabolite
Norethynodrel (Enidre) is a 19-nortestosterone derivative to be used as a progestagen. Norethynodrel can be used for researching inhibition of ovulation . Norethynodrel is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

HY-W782485

Anhydrolutein III Deoxylutein I; Provitamin A2	Structural Classification Natural Products Polygonaceae Source classification Rumex rugosus Campd. Plants	Drug Derivative
Anhydrolutein III (Deoxylutein I) is a dehydration product of Lutein (HY-N6947) .

HY-N8549A

5-Dihydrocortisone	Structural Classification Classification of Application Fields Cardiacglycosides Source classification Metabolic Disease Endogenous metabolite Disease Research Fields Steroids	Endogenous Metabolite
5-Dihydrocortisone is a 5-Dihydrocortisone with mixture of isomers. 5β-Dihydrocortisone is a sterol metabolite of cortisone by 5β-reductase (AKR1D1) in liver

HY-N1651

2,3',4,6-Tetrahydroxybenzophenone	Structural Classification Gentiana lutea L. Source classification Gentianaceae Phenols Polyphenols Plants	Others
2,3',4,6-Tetrahydroxybenzophenone, a kind of benzophenone, is the immediate precursor of xanthones in higher plants .

HY-Y0320R

Dimethyl sulfoxide (Standard) DMSO, meets analytical specification of Ch.P. (Standard)	Microorganisms Source classification	Reference Standards Cholinesterase (ChE) Bacterial
Dimethyl sulfoxide (Standard) is the analytical standard of Dimethyl sulfoxide. This product is intended for research and analytical applications. Dimethyl sulfoxide (DMSO) is an aprotic solvent that dissolves both polar and nonpolar compounds. Dimethyl sulfoxide has anti-freezing and bacteriostatic properties .

HY-N15293

Sesamolinol	Structural Classification Monophenols Sesamum indicum Linn. Source classification Phenols Pedaliaceae Plants	Others
Sesamolinol is a lignin. Sesamolinol is found in sesame seeds. Sesame seed lignans are considered responsible for a number of beneficial health effects including lowering of plasma cholesterol levels and elevation of γ-tocopherol levels .

HY-N15182

4-Trehalosamine	Structural Classification Microorganisms Antibiotics Source classification	Bacterial Drug Derivative
4-Trehalosamine is a derivative of trehalose with weak antibacterial activity. 4-Trehalosamine shows no toxic effects when injected intravenously into mice at a dose of 625 mg/kg .

HY-N0244

Theaflavin-3'-gallate 2 Publications Verification	Structural Classification Flavonoids Classification of Application Fields Flavanols Source classification Phenols Polyphenols Camellia sinensis (L.) O. Ktze. Plants Disease Research Fields Theaceae Cancer	Xanthine Oxidase Apoptosis Necroptosis
Theaflavin-3'-gallate is a monomer of theaflavins found in black tea, which has anti-UVB damage activity and inhibits cell apoptosis and necroptosis. Theaflavin-3'-gallate acts as a pro-oxidant and induces oxidative stress in cancer cells, inhibiting xanthine oxidase (OX), with an IC₅₀ of 7.6 μM .

HY-N9686

Caffeoyl-CoA	Natural Products Gramineae Source classification Secale cereale Plants	Others
Caffeoyl-CoAcould be isolated from leaf tissues of Gramineae with a K_m value of 1.45 μM .

HY-N9075

9-(4′-Hydroxyphenyl)-2-methoxyphenalen-1-one	Structural Classification Monophenols Source classification Phenols Musaceae Plants Musa basjoo Sieb. et Zucc.	Glycosidase
9-(4′-Hydroxyphenyl)-2-methoxyphenalen-1-one is a phytoalexin and mixed competitive α-glucosidase inhibitor of Bacillus stearothermophilus (IC₅₀: 3.86 mg/L) .

HY-113403

Pyridinoline	Structural Classification Animals Ketones, Aldehydes, Acids Source classification	Endogenous Metabolite
Pyridinoline, a fluorescent material, is a bone resorption biomarker. Pyridinoline also is a type crosslink of collagen .

HY-122416

6,8-Diprenylnaringenin Lonchocarpol A; Senegalensin	Structural Classification Classification of Application Fields Erythrinasenegalensis DC. Source classification Metabolic Disease Plants Moraceae Flavonoids Leguminosae Humulus lupulus L. Flavonones Phenols Polyphenols Disease Research Fields Cancer	BCRP
6,8-Diprenylnaringenin (Lonchocarpol A; Senegalensin), a hop prenylflavonoid, is a inhibitor of breast cancer resistance protein (BCRP/ABCG2). 6,8-Diprenylnaringenin inhibits ABCG2-mediated efflux of Mitoxantrone, and ³H-Methotrexate transport (IC₅₀=0.41 μM) in HEK293 cells. 6,8-Diprenylnaringenin exhibits some estrogenicity, but its potency is less than 1% of that of 8-Prenylnaringenin .

HY-113434B

5-HETE (±)-5-HETE	Structural Classification Classification of Application Fields Ketones, Aldehydes, Acids Source classification Endogenous metabolite Inflammation/Immunology Disease Research Fields	Endogenous Metabolite
5-HETE ((±)-5-HETE), a fatty acid, is a oxidative derivative of Arachidonic acid. 5-HETE is a mixture of 5(S)-HETE and 5(R)-HETE. 5-HETE is a potent aggregating agent that induces the aggregation of neutrophils with an IC₅₀ value of 200 nM .

HY-N0015

Astragalin 5+ Cited Publications Astragaline; 3-Glucosylkaempferol; Kaempferol 3-β-D-glucopyranoside	Flavonols Structural Classification Classification of Application Fields Source classification Plants Flavonoids Microorganisms Phenols Polyphenols Disease Research Fields Thesium chinense Turcz. Santalaceae Cancer	Apoptosis NF-κB
Astragalin (Astragaline) a flavonoid with anti-inflammatory, antioxidant, anticancer, bacteriostatic activity. Astragalin inhibits cancer cells proliferation and migration, induces apoptosis. Astragalin is orally active and provides nerve and heart protection, and resistance against and osteoporosis .

HY-Y1787

Dimethyl malonate 4 Publications Verification	Structural Classification Natural Products Source classification Melia azedarach L. Plants Meliaceae	Apoptosis
Dimethyl malonate is a competitive inhibitor of succinate dehydrogenase (SDH). Dimethyl malonate is able to cross the blood-brain barrier and hydrolyse to malonate. Dimethyl malonate reduces neuronal apoptosis .

HY-117586

9-PAHPA	Structural Classification Classification of Application Fields Ketones, Aldehydes, Acids Source classification Metabolic Disease Endogenous metabolite Inflammation/Immunology Disease Research Fields	Endogenous Metabolite
9-PAHPA is a fatty acid esters of hydroxy fatty acid (FAHFA). FAHFAs are a new family of endogenous lipids, have antidiabetic and anti-inflammatory effects .

HY-N4107

Phyllanthin 1 Publications Verification	Phyllanthus urinaria Linn. Structural Classification Classification of Application Fields Source classification Lignans Metabolic Disease Euphorbiaceae Phenylpropanoids Plants Disease Research Fields	TGF-beta/Smad
Phyllanthin is an effective oral anticancer agent. Phyllanthin inhibits MOLT-4 cell viability, increases apoptosis, inhibits cell migration and invasion. Phyllanthin exerts anti-fibrotic effects by down-regulating TGF signaling pathway via ALK5 and Smad2/3. Phyllanthin also has anti-inflammatory and antibacterial properties .

HY-N4107R

Phyllanthin (Standard)	Phyllanthus urinaria Linn. Structural Classification Source classification Lignans Euphorbiaceae Phenylpropanoids Plants	Reference Standards TGF-beta/Smad
Phyllanthin (Standard) is the analytical standard of Phyllanthin. This product is intended for research and analytical applications. Phyllanthin is an effective oral anticancer agent. Phyllanthin inhibits MOLT-4 cell viability, increases apoptosis, inhibits cell migration and invasion. Phyllanthin exerts anti-fibrotic effects by down-regulating TGF signaling pathway via ALK5 and Smad2/3. Phyllanthin also has anti-inflammatory and antibacterial properties .

HY-N0750

Monocrotaline 30+ Cited Publications Crotaline	Structural Classification Alkaloids Pyrrole Alkaloids Classification of Application Fields Leguminosae Crotalaria pallida Ait. Plants Disease Research Fields Cancer	Others
Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC₅₀s of 36.8 µM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. ^[2][6][8].

HY-W013935R

Bisphenol B (Standard)	Structural Classification Source classification Phenols Polyphenols Endogenous metabolite	Reference Standards Endogenous Metabolite Estrogen Receptor/ERR Reactive Oxygen Species (ROS)
Bisphenol B (Standard) is the analytical standard of Bisphenol B. This product is intended for research and analytical applications. Bisphenol B is a close structural analog of Bisphenol A (BPA) (HY-18260). Bisphenol B is a potent, orally active endocrine disruptor (ED). Bisphenol B binds to G protein-coupled estrogen receptor (GPER) (IC₅₀ = 3.3 μM) with higher affinity and agonistic activity than BPA. Bisphenol B promotes GPER mediated cell migration. Bisphenol B exerts estrogenic effects via GPER pathway at nanomolar concentration. Bisphenol B is used in the manufacture of polycarbonate resin with ED properties .

HY-N8394

Eupatolide	Source classification Plants Compositae Guilandina minax (Hance) G. P. Lewis	Others
Eupatolide is an antitumor agent that can be isolated from Eupatorium formosanum. Eupatolide has cytotoxic activity and inhibits human epidermoid carcinoma of larynx cell growth in vitro .

HY-N12239

Condurango glycoside E	Apocynaceae Marsdenia cundurango Rchb.f. Source classification Plants	Others
Condurango glycoside E is a glycoside compound that can be isolated from the bark extract of Marsdenia cundurango .

HY-113410

3-Methylglutaric acid	Structural Classification Classification of Application Fields Source classification Endocrine diseases Metabolic Disease Endogenous metabolite Human Gut Microbiota Metabolites Microorganisms Ketones, Aldehydes, Acids Disease markers Nervous System Disorder Disease Research Fields Cardiovascular System Disorder	Na+/K+ ATPase Mitochondrial Metabolism Reactive Oxygen Species (ROS)
3-Methylglutaric acid is a non-selective inhibitor of mitochondrial function and Na ⁺, K ⁺-ATPase, with an inhibition rate of 30% on rat cortical synaptosomal Na ⁺, K ⁺-ATPase. 3-Methylglutaric acid can induce reactive oxygen species (ROS) generation, thereby causing oxidative damage and inhibiting mitochondrial redox potential and ion pump function of cell membranes. 3-Methylglutaric acid can be used to study the neuropathological mechanisms of metabolic diseases and the role of oxidative stress-mediated neuronal damage in neurodegeneration .

HY-113410R

3-Methylglutaric acid (Standard)	Structural Classification Human Gut Microbiota Metabolites Microorganisms Ketones, Aldehydes, Acids Source classification Disease markers Endocrine diseases Nervous System Disorder Endogenous metabolite Cardiovascular System Disorder	Reference Standards Na+/K+ ATPase Mitochondrial Metabolism Reactive Oxygen Species (ROS)
3-Methylglutaric acid (Standard) is the analytical standard of 3-Methylglutaric acid (HY-113410). This product is intended for research and analytical applications. 3-Methylglutaric acid is a non-selective inhibitor of mitochondrial function and Na ⁺, K ⁺-ATPase, with an inhibition rate of 30% on rat cortical synaptosomal Na ⁺, K ⁺-ATPase. 3-Methylglutaric acid can induce reactive oxygen species (ROS) generation, thereby causing oxidative damage and inhibiting mitochondrial redox potential and ion pump function of cell membranes. 3-Methylglutaric acid can be used to study the neuropathological mechanisms of metabolic diseases and the role of oxidative stress-mediated neuronal damage in neurodegeneration .

HY-W017423

(-)-Carvone	Structural Classification Microorganisms Ketones, Aldehydes, Acids Gymnaster koraiensis Source classification Umbelliferae Plants	Cholinesterase (ChE)
(-)-Carvone is an insect neurotoxin and a irreversible acetylcholinesterase (AChE) inhibitor. (-)-Carvone can be used as a bird repellent, inhibits larval growth, decreases pupatation rate, and increases mortality of larvae .

HY-W017423R

(-)-Carvone (Standard)	Structural Classification Microorganisms Ketones, Aldehydes, Acids Gymnaster koraiensis Source classification Umbelliferae Plants	Reference Standards Cholinesterase (ChE)
(-)-Carvone (Standard) is the analytical standard of (-)-Carvone. This product is intended for research and analytical applications. (-)-Carvone is an insect neurotoxin and a irreversible acetylcholinesterase (AChE) inhibitor. (-)-Carvone can be used as a bird repellent, inhibits larval growth, decreases pupatation rate, and increases mortality of larvae .

HY-128850

N-Acetyl-D-mannosamine N-Acetylmannosamine; ManNAc	Structural Classification Natural Products Human Gut Microbiota Metabolites Neurological Disease Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields	Endogenous Metabolite
N-Acetyl-D-mannosamine (ManNAc) is an oral active sialic acid precursor that can prevent hypertension by increasing sialylation of IgG, making it a promising candidate for cardiovascular disease research. Additionally, N-Acetyl-D-mannosamine can activate hypocretin (HCRT) gene expression in orexin neurons and improve neurodegeneration caused by aging, offering potential avenues for research in neurological disorders .

HY-W013935

Bisphenol B	Structural Classification Classification of Application Fields Source classification Phenols Polyphenols Endogenous metabolite Disease Research Fields Endocrinology	Endogenous Metabolite Estrogen Receptor/ERR Reactive Oxygen Species (ROS)
Bisphenol B is a close structural analog of Bisphenol A (BPA) (HY-18260). Bisphenol B is a potent, orally active endocrine disruptor (ED). Bisphenol B binds to G protein-coupled estrogen receptor (GPER) (IC₅₀ = 3.3 μM) with higher affinity and agonistic activity than BPA. Bisphenol B promotes GPER mediated cell migration. Bisphenol B exerts estrogenic effects via GPER pathway at nanomolar concentration. Bisphenol B is used in the manufacture of polycarbonate resin with ED properties .

HY-N10378

Rubrofusarin 6-O-β-D-glucopyranoside	Monophenols Classification of Application Fields Neurological Disease Source classification Phenols Metabolic Disease Caesalpiniaceae Cassia obtusifolia (L.) H. S. Irwin & Barneby Plants Disease Research Fields	Phosphatase
Rubrofusarin 6-O-β-D-glucopyranoside, the glycoside of Rubrofusarin, is a protein tyrosine phosphatase 1B (PTP1B) inhibitor with the IC₅₀ of 87.36 μM. Rubrofusarin 6-O-β-D-glucopyranoside can be used for the research of comorbid diabetes and depression .

HY-128850R

N-Acetyl-D-mannosamine (Standard) N-Acetylmannosamine (Standard); ManNAc (Standard)	Structural Classification Natural Products Human Gut Microbiota Metabolites Source classification Endogenous metabolite	Reference Standards Endogenous Metabolite
N-Acetyl-D-mannosamine (Standard) is an analytical standard for N-Acetyl-D-mannosamine. This product is intended for research and analytical applications. N-Acetyl-D-mannosamine (ManNAc) is an orally active sialic acid (Sialic Acid) precursor that can prevent hypertension by increasing sialylation of IgG and has potential for use in cardiovascular disease research. N-Acetyl-D-mannosamine activates hypocretin (HCRT) gene expression and alters

HY-N3002

α-Arbutin 4-Hydroxyphenyl α-D-glucopyranoside	Structural Classification Monophenols Classification of Application Fields Source classification Phenols Metabolic Disease Cosmetic Research Ericaceae Plants Disease Research Fields	Tyrosinase
α-Arbutin (4-Hydroxyphenyl α-D-glucopyranoside) is a tyrosinase inhibitor, which is used as an effective skin whiteners. α-Arbutin is promising for research of various diseases such as hyperpigmentation disorders, types of cancers, central nervous system disorders, osteoporosis, diabetes .

HY-N1773

5,7,3'-Tri-O-methyl (-)-epicatechin	Structural Classification Machilus thunbergii Sieb. et Zucc. Flavonoids Flavanols Source classification Plants Lauraceae	Others
5,7,3' -tri-O-Methyl (-)-epicatechin (Compound 13) is a phospholipase Cγ1 (PLCγ1) inhibitor. 5,7,3' -tri-o-methyl (-)-epicatechin has a methylene dioxy benzene ring and can express inhibitory activity against PLCγ1. 5,7,3' -tri-O-Methyl (-)-epicatechin can be used in the study of chemotherapy and chemopexic agents for cancer .

HY-N4317

Ethoxysanguinarine 1 Publications Verification	Alkaloids Classification of Application Fields Source classification Quinoline Alkaloids Macleaya cordata (Willd.) R. Br. Plants Disease Research Fields Papaveraceae Cancer	Apoptosis
Ethoxysanguinarine is a benzophenanthridine alkaloid natural product that is mainly found in Macleaya cordata. Ethoxysanguinarine is an inhibitor of protein phosphatase 2A (CIP2A). Ethoxysanguinarine induces cell apoptosis and inhibits colorectal cancer cells growth .

HY-N12763

Sodium new houttuyfonate SNH	Structural Classification Natural Products Saururaceae Houttuynia cordata Thunb. Source classification Plants	Bacterial Renin
Sodium new houttuyfonate (SNH) is a partially reversible NDM-1 inhibitor with an IC₅₀ of 14.2 μM. Sodium new houttuyfonate is an inhibitor against renin and angiotensin I converting enzyme (ACE). Sodium new houttuyfonate can recover the antibacterial activity of Meropenem (HY-13678) against E. coli BL21/pET15b-blaNDM-1 .

HY-N12748

17βH-Gitoxigenin	Apocynaceae Structural Classification Natural Products Source classification Strophanthus divaricatus (Lour.) Hook. & Arn. Plants	Others
17βH-Gitoxigenin is a compound that can be isolated from cell suspension cultures of Stropanthus divaricatus .

Cat. No.	Product Name	Chemical Structure

HY-W653769

Deltamethrin-d5 (Mixture of Diastereomers)
Deltamethrin-d5 (Mixture of Diastereomers) is the deuterium labeled Deltamethrin (Mixture of Diastereomers) .

HY-W744273

Pravastatin-d9 Sodium (mixture of 2 diastereomers)
Pravastatin-d₉ Sodium (mixture of 2 diastereomers) is the deuterium labeled Pravastatin Sodium.

HY-132485S

N-Methyl Pantoprazole-d3 (Mixture of 1 and 3 isomers)
N-Methyl Pantoprazole-d₃ (Mixture of 1 and 3 isomers) is the deuterium labeled N-Methyl Pantoprazole (Mixture of 1 and 3 isomers) .

HY-132676S

Ramiprilat-d5 (Mixture of Diastereomers)
Ramiprilat-d₅ (Mixture of Diastereomers) is the deuterium labeled Ramiprilat (Mixture of Diastereomers) .

HY-A0115S

Ramiprilat-d3 (Mixture of Diastereomers)
Ramiprilat-d₃ (Mixture of Diastereomers) is the deuterium labeled Ramiprilat (Mixture of Diastereomers) .

HY-W766409

Ciclesonide-d11 (Mixture of Diastereomers)
Ciclesonide-d₁₁ (Mixture of Diastereomers) is the deuterium labeled Ciclesonide.

HY-W777700

Cuscohygrine-d6 (mixture of diastereomers)
Cuscohygrine-d₆ (mixture of diastereomers) is the deuterium labeled Cuscohygrine (Mixture of Diastereomers) (HY-N9904).

HY-W777284

Zeranol-d5 (mixture of diastereomers)
Zeranol-d₅ (mixture of diastereomers) is the deuterium labeled Zeranol (HY-N6709). Zeranol, a metabolite of the mycoestrogen zearalenone, is an estrogen receptor agonist. Zeranol is used as a growth promoter of livestock due to its strong estrogenic activity .

HY-W768541

Idarubicinol-d4 (Mixture of Diastereomers)
Idarubicinol-d₄ (Mixture of Diastereomers) is the deuterium labeled Idarubicinol.

HY-W711709

Terameprocol-d12 (Mixture of Diastereomers)
Terameprocol-d₁₂ (Mixture of Diastereomers) is the deuterium labeled 4,4'-(2,3-Dimethylbutane-1,4-diyl)bis(1,2-dimethoxybenzene) (HY-W422348).

HY-151002S

M8 metabolite of Carvedilol-d5
M8 metabolite of Carvedilol-d₅ is the deuterium labeled M8 metabolite of Carvedilol .

HY-W654209

Glycopyrrolate iodide-d3 (mixture of diastereomers)
Glycopyrrolate iodide-d₃ (mixture of diastereomers) is deuterium labeled 3-(2-Cyclopentyl-2-hydroxy-2-phenylacetoxy)-1,1-dimethylpyrrolidin-1-ium iodide .

HY-W100026S

Galaxolide-d6 (mixture of diastereomers) (>80%)
Galaxolide-d₆ (mixture of diastereomers) (>80%) is the deuterium labeled Galaxolide (HY-W100026). Galaxolide can induce estrogenic activity (Estrogen Receptor/ERR), trigger oxidative stress and genotoxicity, and induce EROD and GST (Glutathione S-transferase) enzyme activity .

HY-132382S

β-Sitosterol-d7 (mixture of diasteromers)
β-Sitosterol-d₇ (Mixture of Diastereomers) is the deuterium labeled β-Sitosterol (mixture of diasteromers) .

HY-W018772S15

D-Ribose(mixture of isomers)-13C5

D-Ribose(mixture of isomers)- ¹³C₅ isomers)- ¹³C₅ is the ¹³C labeled D-Ribose(mixture of isomers) . D-Ribose(mixture of isomers) is an energy enhancer, and acts as a sugar moiety of ATP, and widely used as a metabolic therapy supplement for chronic fatigue syndrome or cardiac energy metabolism. D-Ribose(mixture of isomers) is active in protein glycation, induces NF-κB inflammation in a RAGE-dependent manner .

HY-132706S

N-Deformyl Formoterol-d6 Fumarate (Mixture of Diastereomers)
N-Deformyl Formoterol-d₆ Fumarate (Mixture of Diastereomers) is the deuterium labeled N-Deformyl Formoterol Fumarate (Mixture of Diastereomers) .

HY-132637S

Chlorfenvinphos-d10(Mixture of cis-trans isomers)
Chlorfenvinphos-d₁₀(Mixture of cis-trans isomers) is the deuterium labeled Chlorfenvinphos (Mixture of cis-trans isomers) .

HY-134670S

α-Hydroxy Metoprolol-d5 (Mixture of Diastereomers)
α-Hydroxy Metoprolol-d₅ (Mixture of Diastereomers) is the deuterium labeled α-Hydroxy Metoprolol Mixture of Diastereomers .

HY-W758414

Phoxim-d5 (phenyl-d5) (mixture of isomers)
Phoxim-d₅ (phenyl-d₅) (mixture of isomers) is the deuterium labeled Phoxim (HY-B0819). Phoxim is an organic phosphorus pesticide and widely applies worldwide for agricultural purposes .

HY-132379S

Hydroxy Pioglitazone-d5 (M-IV) (Mixture of-diastereomers)
Hydroxy Pioglitazone-d₅ (M-IV) (Mixture of-diastereomers) is the deuterium labeled Hydroxy Pioglitazone (M-IV) (Mixture of-diastereomers) .

HY-12650S

Mirogabalin-13C2,d1 (Mixture of Diastereomers)
Mirogabalin-13C2,d1 (Mixture of Diastereomers) is a C13 and deuterium labeled Mirogabalin. Mirogabalin (DS-5565) is a novel, preferentially selective α2δ-1 ligand characterized by high potency and selectivity to the α2δ-1 subunit of voltage-sensitive calcium channel complexes in the CNS .

HY-W654395

Methyl jasmonate-d5 (mixture of diastereomers)
Methyl jasmonate-d₅ (mixture of diastereomers) is deuterium labeled Methyl (Z)-2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate .

HY-150857S

Thymine-α,α,α,6-d4 Glycol (mixture of diastereomers)-d4
Thymine-α,α,α,6-d₄ Glycol (mixture of diastereomers)-d₄ is the deuterium labeled Thymine-α,α,α,6-d4 Glycol (mixture of diastereomers) .

HY-113026S

(2RS,4R,8R)-δ-Tocopherol-d4 (Mixture of Diastereomers)
(2RS,4R,8R)-δ-Tocopherol-d₄ (Mixture of Diastereomers) is the deuterium labeled (2RS,4R,8R)-δ-Tocopherol (Mixture of Diastereomers) .

HY-W744215

3-Hydroxy tibolone-d5 (mixture of 3a & 3b isomers)
3-Hydroxy tibolone-d₅ (mixture of 3a & 3b isomers) is the deuterium labeled 3-Hydroxy tibolone.

HY-12040S

Elesclomol-d2

Elesclomol-d₂ (STA-4783-d₂) is a deuterium labeled Elesclomol (HY-12040). Elesclomol (STA-4783) is a potent copper ionophore and promotes copper-dependent cell death (cuproptosis). Elesclomol specifically binds ferredoxin 1 (FDX1) α2/α3 helices and β5 strand. Elesclomol inhibits FDX1-mediated Fe-S cluster biosynthesis. Elesclomol is an oxidative stress inducer that induces cancer cell apoptosis. Elesclomol is a reactive oxygen species (ROS) inducer. Elesclomol can be used for Menkes and associated disorders of hereditary copper deficiency research .

HY-W768491

3',5'-Di-O-benzyl Entecavir-13C2,15N
3',5'-Di-O-benzyl Entecavir- ¹³C₂, ¹⁵N (The intermediate of Entecavir hydrate- ¹³C₂, ¹⁵N) is the ¹³C- and ¹⁵N-labeled 2-Amino-9-((1S,3R,4S)-4-(benzyloxy)-3-((benzyloxy)methyl)-2-methylenecyclopentyl)-1H-purin-6(9H)-one (HY-W105415).

HY-152040S

Tenuazonic acid-(acetyl-13C2) (mixture of diastereomers) in methanol
Tenuazonic acid-(acetyl- ¹³C₂) (mixture of diastereomers) in methanol (3-(Acetyl- ¹³C₂)-5-((S)-sec-butyl)-4-hydroxy-1,5-dihydro-2H-pyrrol-2-one) is ¹³C labeled Tenuazonic acid-(acetyl) (mixture of diastereomers) in methanol .

HY-B1258S

Intermediate of tranexamic Acid-13C2,15N
Intermediate of tranexamic Acid- ¹³C₂, ¹⁵N (Aminomethylbenzoic acid- ¹³C₂, ¹⁵N) is ¹³C and ¹⁵N labeled 4-(Aminomethyl)benzoic acid. 4-(Aminomethyl)benzoic acid is a competitive inhibitor of PepT1 and has antifibrinolytic activity .

Inquiry Online

Your information is safe with us. * Required Fields.

MCE Japan Authorized Agent ナミキ商事株式会社コスモ・バイオ株式会社重松貿易株式会社
Salutation			Country or Region *
Applicant Name *			Organization Name *
Department *
Email Address *			Product Name *
Cat. No.			Requested quantity *
Phone Number *
Remarks