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( )-Hosenkoside F

" in MedChemExpress (MCE) Product Catalog:

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2023

Inhibitors & Agonists

Screening Libraries

Fluorescent Dye

Biochemical Assay Reagents

Peptides

MCE Kits

Inhibitory Antibodies

340

Natural
Products

340

Recombinant Proteins

Isotope-Labeled Compounds

155

Antibodies

Click Chemistry

312

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-N2241

Hosenkoside F (+)-Hosenkoside F	Others	Inflammation/Immunology
Hosenkoside F is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2244

Hosenkoside M (+)-Hosenkoside M	Others	Inflammation/Immunology
Hosenkoside M is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2249

Hosenkoside A	Others	Inflammation/Immunology
Hosenkoside A is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2249R

Hosenkoside A (Standard)	Reference Standards Others	Inflammation/Immunology
Hosenkoside A (Standard) is the analytical standard of Hosenkoside A. This product is intended for research and analytical applications. Hosenkoside A is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2250R

Hosenkoside B (Standard)	Reference Standards Others	Inflammation/Immunology
Hosenkoside B (Standard) is the analytical standard of Hosenkoside B. This product is intended for research and analytical applications. Hosenkoside B is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2243R

Hosenkoside K (Standard)	Reference Standards Others	Inflammation/Immunology
Hosenkoside K (Standard) is the analytical standard of Hosenkoside K. This product is intended for research and analytical applications. Hosenkoside K is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2251R

Hosenkoside C (Standard)	Reference Standards Others	Others
Hosenkoside C (Standard) is the analytical standard of Hosenkoside C. This product is intended for research and analytical applications. Hosenkoside C is a baccharane glycoside isolated from the seeds of Impatiens balsamina .

HY-N12052

Hosenkoside L	Others	Others
Hosenkoside L is a baccharane-type glycoside .

HY-N12050

Hosenkoside D	Others	Others
Hosenkoside D is a baccharane-type glycoside .

HY-N12054

Hosenkoside O	Others	Others
Hosenkoside O is a baccharane glycoside isolated from lmpatiens buhamina .

HY-N2243

Hosenkoside K	Others	Inflammation/Immunology
Hosenkoside K is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N12053

Hosenkoside N	Others	Others
Hosenkoside N is a baccharane glycoside isolated from lmpatiens buhamina .

HY-N2250

Hosenkoside B	Others	Inflammation/Immunology
Hosenkoside B is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2251

Hosenkoside C	Others	Others
Hosenkoside C is a baccharane glycoside isolated from the seeds of Impatiens balsamina .

HY-N12051

Hosenkoside E	Biochemical Assay Reagents	Others
Hosenkoside E is a natural product that can be obtained from the seeds of Impatiens balsamina .

HY-N2242

Hosenkoside G	Others	Cancer
Hosenkoside G, a baccharane glycoside isolated from the seeds of Impatiens Balsamina L., possesses anti-tumor activity .

HY-N12604

Penicisteck acid F	NF-κB	Others
Penicisteck acid F (Compound 2) is a Marine derived tanzanic acid derivative that is a NF-κB inhibitor. Penicisteck acid F inhibits osteoclast expression by decreasing RANKL-induced IκBα degradation, NF-κB p65 nuclear translocation, NFATc1 activation and nuclear translocation, and related mRNA expression. Penicisteck acid F can be used in osteoporosis research .

HY-N1208

Spiradine F O-Acetylspiradine G; Spiradine G acetate	Others	Cardiovascular Disease
Spiradine F is a main alkaloidal component of spiraea japonioa L. fil. Spiradine F derivative can inhibit platelet-activating factor (PAF)-induced platelet aggregation .

HY-N16392

14-epi-Berkeleylactone F	Endogenous Metabolite	Infection
14-epi-Berkeleylactone F (Compound 8) is a C-14 epimer of Berkeleylactone F (HY-N8386). 14-epi-Berkeleylactone F can be isolated from Penicillium turbatum NRRL 5630. 14-epi-Berkeleylactone F has no significant biological activity against bacterium (Staphylococcus aureus, Bacillus subtilis and E. coli), fungi Candida albicans, the parasite Giardia duodenalis and NS-1 murine myeloma cells .

HY-113246

15-keto-Prostaglandin F2a 15-keto-PGF2α	Prostaglandin Receptor Endogenous Metabolite	Endocrinology
15-keto-Prostaglandin F2α (15-keto-PGF2α) is a metabolite of Prostaglandin F2α. Prostaglandin F2α. Prostaglandin F2α is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist and plays a key role in the onset and progression of labour .

HY-146232

F 13714 F 14679	5-HT Receptor	Others
F 13714 (F 14679) is a prototypical 5-HT_1A agonist with a pK_i of 10.23. F 13714 induces large Ca ²⁺ responses .

HY-P990221

Anti-Mouse IL-17F Antibody (MM17F8F5.1A9)	Interleukin Related	Infection Neurological Disease Cancer
Anti-Mouse IL-17F Antibody (MM17F8F5.1A9) is a mouse-derived IgG1 κ type antibody inhibitor, targeting to mouse *IL-17F. Anti-Mouse IL-17F Antibody (MM17F8F5.1A9) can neutralize IL-17. Anti-Mouse IL-17F Antibody (MM17F8F5.1A9*) can be used for the researches of cancer, infection and neurological disease, such as Alzheimer’s disease (AD) and pancreatic cancer .

HY-N15473

Isopaucifloral F (±)-Isopaucifloral F	Estrogen Receptor/ERR Drug Derivative	Inflammation/Immunology
Isopaucifloral F ((±)-Isopaucifloral F) is a Resveratrol (HY-16561)-derived sesquiterpenes. Isopaucifloral F is an orally active ERβ agonist (EC₅₀: 46.96 μM). Isopaucifloral F has antiosteoporosis activity. LD₅₀ in rats: > 5 mg/kg .

HY-115969

F-17	Bacterial	Infection
F-17 is a potential inhibitor of virulence factor. F-17 shows very significant inhibitory effect on biofilm, elastase, pyocyanin, and swarming motility. F-17 also shows a good binding effect on LasR and PqsR. F-17 has no obvious cytotoxicity .

HY-P2098

Alamethicin F 50	Antibiotic Bacterial Fungal	Infection
Alamethicin F 50 is an antibiotic. Alamethicin F 50 is composed of membrane-active peptide, containing 75% Alamethicin F 50/5 and 10% Alamethicin F 50/7. Alamethicin F 50 is exhibits antifungal and antibacterial activity by disrupting the integrity of microbial cell membranes, resulting in leakage of cell contents and death of the microorganisms. Alamethicin F 50 is able to reduce the surface tension of water, which can be used as a surfactant or detergent .

HY-106902

F-1394	Acyltransferase	Cardiovascular Disease
F-1394 is an orally active acyl-CoA:cholesterol acyltransferase (ACAT) inhibitor that inhibits dietary cholesterol absorption in mice. F-1394 can be used in cardiovascular disease research .

HY-113824

RID-F Ridaifen-F	Proteasome	Cancer
RID-F (Ridaifen-F), a Tamoxifen (HY-13757A) derivative, is a nonpeptidic proteasome inhibitor. RID-F inhibits human 20S proteasome activity, with IC₅₀s of 0.64, 0.34, and 0.43 μM for CT-L, T-L, and PGPH, respectively .

HY-125349

A-83016F	Antibiotic	Infection
A-83016F is an antibiotic. A-83016F has weak antimicrobial activity. A-83016F can be isolated from the culture broth of an unidentified actinomycete designated A83016 .

HY-N6217

F-14329	Endogenous Metabolite	Others
F-14329 is a tetramic acid fungal metabolite .

HY-N7223

Lappaol F	YAP Apoptosis	Cancer
Lappaol F, a lignin, is an anticancer agent. Lappaol F inhibits YAP mRNA and protein level. Lappaol F inhibits tumor cell growth by inducing cell cycle arrest. Lappaol F induces cancer cell apoptosis, and inhibits tumor growth. Lappaol F can be isolated from Arctium lappa Linne (Asteraceae) .

HY-176362S

4-F-Benzenesulfonate-pyrrole(2-F-Ph)-methylamine-d3	Isotope-Labeled Compounds	Others
4-F-Benzenesulfonate-pyrrole(2-F-Ph)-methylamine-d₃ is the deuterium labeled 4-F-Benzenesulfonate-pyrrole(2-F-Ph)-methylamine.

HY-D0159

ZnAF-1F	Fluorescent Dye	Others
ZnAF-1F is a potent fluorophore for with an K_d value of 2.2 nM. ZnAF-1F can be used as fluorescent probes for Zn ²⁺ in cells. ZnAF-1F shows λ excitation of 489 nm and λ emission of 514 nm .

HY-106031

F-14512	Topoisomerase	Cancer
F-14512 is a targeted cytotoxic compound that utilizes the polyamine transport system (PTS) to selectively deliver polyamine-containing drugs to cancer cells. F-14512 combines an epipodophyllotoxin core that targets topoisomerase II with a spermine group that acts as a cell delivery vehicle, with improved selectivity for tumor cells. F-14512 exhibits significant cytotoxicity against cells with high PTS activity and demonstrates high potency in multiple human cell lines (median IC₅₀=0.18 μM). In the MX1 breast tumor xenograft model, F-14512 exhibits potent antitumor activity .

HY-19886

F 16915	Drug Intermediate	Cardiovascular Disease
F 16915, a Docosahexaenoic Acid (DHA, HY-B2167) derivative, is a potent pro-agent of DHA. F 16915 can prevent heart failure-induced atrial fibrillation .

HY-N8619

Minimolide F	Others	Cancer
Minimolide F is a sesquiterpene lactone. Minimolide F has inhibitory activity against human nasopharyngeal cancer cells. Minimolide F can be used for the research of cancer .

HY-N10952

Epicornuin F	Others	Cancer
Epicornuin F is a prenylated flavonoid. Epicornuin F can be isolated from the leaves of Epimedium brevicornu. Epicornuin F has the cytotoxic activity against HepG2 cells with an IC₅₀ value of 33.4 μM. Epicornuin F can be used for the research of cancer .

HY-153839

ODN 4084-F	Toll-like Receptor (TLR)	Inflammation/Immunology
ODN 4084-F is a class B (‘broadly-active’) inhibitory ODN. ODN 4084-F is potent inhibitor of TLR9-induced B cells and macrophages.

HY-153839A

ODN 4084-F sodium	Toll-like Receptor (TLR)	Inflammation/Immunology
ODN 4084-F sodium is a class B (‘broadly-active’) inhibitory ODN. ODN 4084-F sodium is potent inhibitor of TLR9-induced B cells and macrophages.

HY-N10380

Inonotusol F	Others	Metabolic Disease
Inonotusol F is a triterpene isolated from Inonotus obliquus. Inonotusol F shows hepatoprotective effects against D-galactosamine-induced WB-F344 cell damage .

HY-15583

Auristatin F	ADC Payload Microtubule/Tubulin	Cancer
Auristatin F is a potent cytotoxin in antibo-conjugated agents and an analogue of MMAF. Auristatin F is a potent microtubule inhibitor and vascular damaging agent (VDA). Auristatin F inhibits cell division by preventing tubulin aggregation.Auristatin F can be used in antibody-drug conjugates (ADC) .

HY-162142

BB2-50F	Bacterial Succinate Dehydrogenase Reactive Oxygen Species (ROS)	Infection
BB2-50F is an antimicrobial agent and succinate dehydrogenase and *F1Fo-ATP* synthase inhibitor. BB2-50F induces ROS. BB2-50F inhibits succinate oxidation and reduces tricarboxylic acid (TCA) cycle activity. BB2-50F inhibits the growth of Mycobacterium tuberculosis H37Rv and its auxotrophic, attenuated derivative mc2 6230 (ΔRD1, ΔpanCD) with an MIC of 8 μM .

HY-N10471

F3226-1387	Parasite Endogenous Metabolite	Infection
F3226-1387 is a potent Entamoeba histolytica O-acetylserine sulfhydrylase EhOASS3 inhibitor with an IC₅₀ value of 38 μM. F3226-1387 can suppress the growth of the amoeba .

HY-161758

F0045(S)	Influenza Virus	Infection
F0045(S) is a potent influenza hemagglutinin inhibitor with a K_D value of 6.1 µM. F0045(S) protects human cells from influenza infection .

HY-172958

F6524-1593	Anaplastic lymphoma kinase (ALK)	Cancer
F6524-1593 is an ALK inhibitor. F6524-1593 has inhibitory activity against A549 and HepG-2 cells with IC₅₀ values of 161.1 μM and 91.03 μM, respectively. F6524-1593 can be used in the research of ALK-related cancers (such as non-small cell lung cancer, lymphoma and neuroblastoma) .

HY-N11430

F1839-I	HIV	Infection
F1839-I is a compound that can be isolated from Stachybotrys. F1839-I has weak cytotoxicity and anti-HIV activity with an IC₅₀ value of 15.6 μM .

HY-138881

Lenalidomide-6-F	Ligands for E3 Ligase	Cancer
Lenalidomide-6-F is the Lenalidomide-based cereblon (CRBN) ligand used in the recruitment of CRBN protein. Lenalidomide-6-F can be connected to the ligand for protein by a linker to form PROTAC .

HY-N14022

Glidobactin F	Antibiotic Fungal	Infection Cancer
Glidobactin F is an anti-tumor antibiotic. Glidobactin F has the activity against pathogenic fungi and yeast. Glidobactin F also extends the survival of mice inoculated with leukemia P388 cells .

HY-124421R

5F-203 (Standard)	Aryl Hydrocarbon Receptor	Others
5F-203 (Standard) is the analytical standard of 5F-203. This product is intended for research and analytical applications. 5F-203 (NSC-703786) is a cytotoxic molecule that forms DNA adducts and cell cycle arrest. 5F-203 induces aryl hydrocarbon receptor (AhR) signaling and elevates expression of CYP1A1. 5F-203 also increases the levels of reactive oxygen species as well as activates JNK, ERK, and p38 .

HY-N14078

Monamycin F	Antibiotic Bacterial	Infection
Monamycin F is an ester peptide antibiotic. Monamycin F has activity against Gram-positive bacteria .

HY-133220A

Guajadial F	Others	Cancer
Guajadial F is a natural product that can be found in Psidium guajava. Guajadial F shows cytotoxicity .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N2241

Hosenkoside F (+)-Hosenkoside F	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants Inflammation/Immunology Disease Research Fields	Others
Hosenkoside F is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2244

Hosenkoside M (+)-Hosenkoside M	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants Inflammation/Immunology Disease Research Fields	Others
Hosenkoside M is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2249

Hosenkoside A	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants Inflammation/Immunology Disease Research Fields	Others
Hosenkoside A is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2249R

Hosenkoside A (Standard)	Triterpenes Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants	Reference Standards Others
Hosenkoside A (Standard) is the analytical standard of Hosenkoside A. This product is intended for research and analytical applications. Hosenkoside A is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2250R

Hosenkoside B (Standard)	Triterpenes Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants	Reference Standards Others
Hosenkoside B (Standard) is the analytical standard of Hosenkoside B. This product is intended for research and analytical applications. Hosenkoside B is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2243R

Hosenkoside K (Standard)	Triterpenes Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants	Reference Standards Others
Hosenkoside K (Standard) is the analytical standard of Hosenkoside K. This product is intended for research and analytical applications. Hosenkoside K is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2251R

Hosenkoside C (Standard)	Triterpenes Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants	Reference Standards Others
Hosenkoside C (Standard) is the analytical standard of Hosenkoside C. This product is intended for research and analytical applications. Hosenkoside C is a baccharane glycoside isolated from the seeds of Impatiens balsamina .

HY-N12052

Hosenkoside L	Polysaccharides Source classification Impatiens balsamina Linn. Balsaminaceae Plants Saccharides	Others
Hosenkoside L is a baccharane-type glycoside .

HY-N12050

Hosenkoside D	Polysaccharides Source classification Impatiens balsamina Linn. Balsaminaceae Plants Saccharides	Others
Hosenkoside D is a baccharane-type glycoside .

HY-N12054

Hosenkoside O	Polysaccharides Source classification Impatiens balsamina Linn. Balsaminaceae Plants Saccharides	Others
Hosenkoside O is a baccharane glycoside isolated from lmpatiens buhamina .

HY-N2243

Hosenkoside K	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants Inflammation/Immunology Disease Research Fields	Others
Hosenkoside K is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N12053

Hosenkoside N	Polysaccharides Source classification Impatiens balsamina Linn. Balsaminaceae Plants Saccharides	Others
Hosenkoside N is a baccharane glycoside isolated from lmpatiens buhamina .

HY-N2250

Hosenkoside B	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Plants Inflammation/Immunology Disease Research Fields	Others
Hosenkoside B is a baccharane glycoside isolated from the seeds of impatiens balsamina.

HY-N2251

Hosenkoside C	Triterpenes Classification of Application Fields Terpenoids Impatiens balsamina Linn. Source classification Balsaminaceae Other Diseases Plants Disease Research Fields	Others
Hosenkoside C is a baccharane glycoside isolated from the seeds of Impatiens balsamina .

HY-N12051

Hosenkoside E	Polysaccharides Source classification Impatiens balsamina Linn. Balsaminaceae Plants Saccharides	Biochemical Assay Reagents
Hosenkoside E is a natural product that can be obtained from the seeds of Impatiens balsamina .

HY-N2242

Hosenkoside G	Triterpenes Classification of Application Fields Terpenoids Source classification Impatiens balsamina Linn. Balsaminaceae Plants Disease Research Fields Cancer	Others
Hosenkoside G, a baccharane glycoside isolated from the seeds of Impatiens Balsamina L., possesses anti-tumor activity .

HY-N12604

Penicisteck acid F	Microorganisms Ketones, Aldehydes, Acids Source classification	NF-κB
Penicisteck acid F (Compound 2) is a Marine derived tanzanic acid derivative that is a NF-κB inhibitor. Penicisteck acid F inhibits osteoclast expression by decreasing RANKL-induced IκBα degradation, NF-κB p65 nuclear translocation, NFATc1 activation and nuclear translocation, and related mRNA expression. Penicisteck acid F can be used in osteoporosis research .

HY-N1208

Spiradine F O-Acetylspiradine G; Spiradine G acetate	Alkaloids Pyrrole Alkaloids Source classification Rosaceae Spiraea japonica Plants	Others
Spiradine F is a main alkaloidal component of spiraea japonioa L. fil. Spiradine F derivative can inhibit platelet-activating factor (PAF)-induced platelet aggregation .

HY-N16392

14-epi-Berkeleylactone F	Natural Products Microorganisms Source classification	Endogenous Metabolite
14-epi-Berkeleylactone F (Compound 8) is a C-14 epimer of Berkeleylactone F (HY-N8386). 14-epi-Berkeleylactone F can be isolated from Penicillium turbatum NRRL 5630. 14-epi-Berkeleylactone F has no significant biological activity against bacterium (Staphylococcus aureus, Bacillus subtilis and E. coli), fungi Candida albicans, the parasite Giardia duodenalis and NS-1 murine myeloma cells .

HY-113246

15-keto-Prostaglandin F2a 15-keto-PGF2α	Classification of Application Fields Ketones, Aldehydes, Acids Source classification Endogenous metabolite Disease Research Fields Endocrinology	Prostaglandin Receptor Endogenous Metabolite
15-keto-Prostaglandin F2α (15-keto-PGF2α) is a metabolite of Prostaglandin F2α. Prostaglandin F2α. Prostaglandin F2α is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist and plays a key role in the onset and progression of labour .

HY-N15473

Isopaucifloral F (±)-Isopaucifloral F	Source classification Phenols Polyphenols Plants Dipterocarpaceae Vatica pauciflora (Korth.) Blume	Estrogen Receptor/ERR Drug Derivative
Isopaucifloral F ((±)-Isopaucifloral F) is a Resveratrol (HY-16561)-derived sesquiterpenes. Isopaucifloral F is an orally active ERβ agonist (EC₅₀: 46.96 μM). Isopaucifloral F has antiosteoporosis activity. LD₅₀ in rats: > 5 mg/kg .

HY-N6217

F-14329	Alkaloids Monophenols Microorganisms Pyrrole Alkaloids Classification of Application Fields Source classification Other Diseases Phenols Disease Research Fields	Endogenous Metabolite
F-14329 is a tetramic acid fungal metabolite .

HY-N7223

Lappaol F	Source classification Lignans Phenylpropanoids Plants Compositae Gueldenstaedtia verna (Georgi) Boriss.	YAP Apoptosis
Lappaol F, a lignin, is an anticancer agent. Lappaol F inhibits YAP mRNA and protein level. Lappaol F inhibits tumor cell growth by inducing cell cycle arrest. Lappaol F induces cancer cell apoptosis, and inhibits tumor growth. Lappaol F can be isolated from Arctium lappa Linne (Asteraceae) .

HY-N8619

Minimolide F	Terpenoids Sesquiterpenes Euchresta horsfieldii (Lesch.) J. Benn. Plants Compositae	Others
Minimolide F is a sesquiterpene lactone. Minimolide F has inhibitory activity against human nasopharyngeal cancer cells. Minimolide F can be used for the research of cancer .

HY-N10952

Epicornuin F	Flavonoids Source classification Phenols Epimedium brevicornu Maxim. Plants Berberidaceae Isoflavones	Others
Epicornuin F is a prenylated flavonoid. Epicornuin F can be isolated from the leaves of Epimedium brevicornu. Epicornuin F has the cytotoxic activity against HepG2 cells with an IC₅₀ value of 33.4 μM. Epicornuin F can be used for the research of cancer .

HY-N10380

Inonotusol F	Natural Products Microorganisms Source classification	Others
Inonotusol F is a triterpene isolated from Inonotus obliquus. Inonotusol F shows hepatoprotective effects against D-galactosamine-induced WB-F344 cell damage .

HY-N10471

F3226-1387	Natural Products Microorganisms Source classification	Parasite Endogenous Metabolite
F3226-1387 is a potent Entamoeba histolytica O-acetylserine sulfhydrylase EhOASS3 inhibitor with an IC₅₀ value of 38 μM. F3226-1387 can suppress the growth of the amoeba .

HY-N11430

F1839-I	Monophenols Microorganisms Source classification Phenols	HIV
F1839-I is a compound that can be isolated from Stachybotrys. F1839-I has weak cytotoxicity and anti-HIV activity with an IC₅₀ value of 15.6 μM .

HY-N14022

Glidobactin F	Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Fungal
Glidobactin F is an anti-tumor antibiotic. Glidobactin F has the activity against pathogenic fungi and yeast. Glidobactin F also extends the survival of mice inoculated with leukemia P388 cells .

HY-N14078

Monamycin F	Microorganisms Macrolide Antibiotics Antibiotics Source classification	Antibiotic Bacterial
Monamycin F is an ester peptide antibiotic. Monamycin F has activity against Gram-positive bacteria .

HY-133220A

Guajadial F	Other Monoterpenes Terpenoids Source classification Psidium guajava Linn. Myrtaceae Plants	Others
Guajadial F is a natural product that can be found in Psidium guajava. Guajadial F shows cytotoxicity .

HY-N16403

Aspergillusidone F	Natural Products Microorganisms Source classification	Cytochrome P450 Endogenous Metabolite Drug Isomer
Aspergillusidone F (Compound 3), a brominated depsidone, is a regioisomer of Aspergillusidone D (HY-N16402). Aspergillusidone F is a Aromatase inhibitor with an IC₅₀ of 0.5  μM. Aspergillusidone F can be isolated from fungus Aspergillus unguis cultured in KBr medium. Aspergillusidone F has potent cytotoxicity against cancers cells, such as MOLT-3 cells. Aspergillusidone F can be used for cancers like breast cancer research .

HY-N0861

Ikarisoside F Ikarisoside-F; Icarisoside-F	Flavonols Flavonoids Classification of Application Fields Source classification Phenols Polyphenols Epimedium brevicornu Maxim. Plants Berberidaceae Disease Research Fields Cancer	Others
Ikarisoside F is a flavonol glycoside from Vancouveria hexandra; could bind to AdoHcy hydrolase.

HY-N12241

Sterebin F	Terpenoids Source classification Cassia Diterpenoids Plants Compositae	Others
Sterebin F is a steroid isolated from the Stevia rebaudiana leaves. Sterebin F has hypoglycemic activity .

HY-N13098

Elatoside F	Triterpenes Terpenoids Source classification Aralia elata (Miq.) Seem. Plants Araliaceae	NF-κB
Elatoside F is a triterpenoid saponin with anti-inflammatory activity. Elatoside F inhibits lipopolysaccharide-induced nitric oxide production and nuclear factor NF-κB activation. Elatoside F can be isolated from Aralia elata in one step.

HY-N10661

Ipomoeassin F Ipom-F	Natural Products Ipomoea squamosa Choisy Plants Convolvulaceae	SARS-CoV
Ipomoeassin F is a potent and selective endoplasmic reticulum (ER) protein-translocation inhibitor by targeting the pore-forming subunit of the Sec61 complex (Sec61α) at the ER membrane. Ipomoeassin F selectively inhibits the ER membrane translocation of SARS-CoV-2 proteins. Ipomoeassin F block the ER translocation of secretory proteins and type I transmembrane proteins (TMPs), but not type III TMPs .

HY-N8386

Berkeleylactone F	Infection Microorganisms Classification of Application Fields Ketones, Aldehydes, Acids Source classification Disease Research Fields	Antibiotic
Berkeleylactone F is an antibiotic macrolide compound. Berkeleylactone F showed modest inhibition of CCRF-CEM leukemia cells .

HY-N3518

Mulberroside F	Monophenols other families Classification of Application Fields Whitening Agent Source classification Phenols Metabolic Disease Cosmetic Research Plants Disease Research Fields	Tyrosinase
Mulberroside F is one of the main bioactive constituents in mulberry (Morus alba L.) . Mulberroside F shows inhibitory effects on tyrosinase activity and on the melanin formation. Mulberroside F also exhibits superoxide scavenging activity that is involved in the protection against auto-oxidation .

HY-N14968

Enniatin F	Natural Products Microorganisms Source classification	Parasite Fungal
Enniatin F has insecticidal and antifungal activity. Enniatin F also can inhibit acyl-CoA, cholesterol acyltransferase (ACAT) .

HY-N14210

Epithienamycin F	Natural Products Microorganisms Source classification	Antibiotic Bacterial
Epithienamycin F is a carbapenem antibiotic. Epithienamycin F has anti-Gram-positive bacteria and anti-Gram-negative bacteria activity .

HY-N3532

Cannabisin F	Monophenols Source classification Phenols Solanaceae Plants Datura metel Linn.	Sirtuin
Cannabisin F is a SIRT1 modulator. Cannabisin F, as a hempseed lignanamide, can be used for the research of anti-inflammatory and anti-oxidative. Cannabisin F may be a potential agent of neurodegenerative diseases as modulators of SIRT1/NF-κB and Nrf2 .

HY-N14396

Sannamycin F	Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Sannamycin F is an aminoglycoside antibiotic. Sannamycin F has weak antibacterial activity against Gram-positive bacteria and Gram-negative bacteria .

HY-N10766

Ampelopsin F	Vitis coignetiae Source classification Phenols Polyphenols Plants Vitaceae	Others
Ampelopsins F is a bridged plant oligostilbene that can be isolated from Ampelopsis brevipedunculata var. hancei roots. Ampelopsins F is a resveratrol dimer .

HY-N12638

Endolide F	Microorganisms Cyclopeptides Source classification	Vasopressin Receptor
Endolide F (Compound 2) is a proline-containing lactone. Endolide F is a moderate antagonist of the arginine antidiuretic hormone V1A receptor .

HY-N13926

Arisugacin F	Natural Products Microorganisms Source classification	Cholinesterase (ChE)
Arisugacin F, a microbial metabolite, is a structural analog of Arisugacin A (HY-N13901). Arisugacin F shows no activity against AChE .

HY-N12339

Wulfenioidin F	Terpenoids Labiatae Ambrosia psilostachya DC. Source classification Diterpenoids Plants	Virus Protease
Wulfenioidin F is a diterpenoid, that can be isolated from the whole plant of Orthosiphon wulfenioides. Wulfenioidin F exhibits activity against Zika virus (ZIKV) with an EC₅₀ of 8.07 μM. Wulfenioidin F interferes with the replication of the ZIKV by inhibiting the expression of the ZIKV envelope (E) protein .

HY-N10017

Lucidone F	Triterpenes Microorganisms Terpenoids Source classification	Others
Lucidone F is a nortriterpenoid analogue which is derivated from Ganoderma resinaceum. Lucidone F is promising for research of immune-regulation, hyperglycemia and liver disease .

HY-N15559

Thaigranatumin F	Natural Products Xylocarpus granatum J. Koenig Source classification Plants Meliaceae	Drug Derivative
Thaigranatumin F is a protolimonoid compound found in the seeds of the Thai mangrove (Xylocarpus granatum). Thaigranatumin F is promising for research of neurodegenerative diseases such as Parkinson's diseases .

HY-N13944

Argyrin F	Natural Products Microorganisms Source classification	Apoptosis
Argyrin F a cyclic peptide with antitumoral activities. Argyrin F inhibits cell proliferation, migration, invasion and colony formation by partial induction of apoptosis and epithelial-mesenchymal transition (EMT). Argyrin F stabilizes p27 ^kip, up-regulated p21 ^waf1/cip1 and depletes COX2. Argyrin F can be used for the study of pancreatic ductal adenocarcinoma (PDAC) .

HY-N6048

Lancifodilactone F	Schisandra lancifolia (Rehd. et Wils.) A. C. Smith Triterpenes Terpenoids Source classification Plants Schisandraceae	HIV
Lancifodilactone F (compound 1) can be isolated from the leaves and stems of Schisandra lancifolia. Lancifodilactone F has anti-HIV activity with EC₅₀=20.69 μg/mL. Lancifodilactone F has cytotoxicity against C8166 cells (CC₅₀ >200 μg/mL) .

Cat. No.	Product Name	Chemical Structure

HY-15583S

Auristatin F-d8
Auristatin F-d₈ is deuterium labeled Auristatin F (HY-15583). Auristatin F is a potent cytotoxin in antibo-conjugated agents and an analogue of MMAF. Auristatin F is a potent microtubule inhibitor and vascular damaging agent (VDA). Auristatin F inhibits cell division by preventing tubulin aggregation.Auristatin F can be used in antibody-drug conjugates (ADC) .

HY-113358S

6-keto Prostaglandin F1α-d4
6-keto Prostaglandin F1α-d₄ is the deuterium labeled 6-keto Prostaglandin F1α .

HY-113459S

Prostaglandin F1a-d9
Prostaglandin F1a-d₉ is the deuterium labeled Prostaglandin F1a .

HY-134178S

5-Fluorouridine 5'-triphosphate-19F
5-Fluorouridine 5'-triphosphate- ¹⁹F is a ¹⁹F labeled 5-Fluorouridine 5'-triphosphate.

HY-114695S

Prostaglandin F2α-1-glyceryl ester-d5
Prostaglandin F2α-1-glyceryl ester-d₅ is the deuterium labeled Prostaglandin F2α-1-glyceryl ester .

HY-137012S

8-iso Prostaglandin F1α-d9
8-iso Prostaglandin F1α-d₉ is the deuterium labeled 8-iso Prostaglandin F1α .

HY-113209S1

8-iso Prostaglandin F2α-d9

8-iso Prostaglandin F2α-d₉ is the deuterium labeled 8-Isoprostaglandin F2α. 8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-113209S2

8-Isoprostaglandin F2α-13C5

8-Isoprostaglandin F2α- ¹³C₅ is ¹³C labeled 8-Isoprostaglandin F2α (HY-113209). 8-Isoprostaglandin F2α is an isoprostane produced by the non-enzymatic peroxidation of arachidonic acid in membrane phospholipids. 8-Isoprostaglandin F2α is present in human plasma in two distinct forms - esterified in phospholipids and as the free acid. 8-Isoprostaglandin F2α is a weak TP receptor agonist in vascular smooth muscle.

HY-113887S

Prostaglandin F1β-d9
Prostaglandin F1β-d₉ is deuterium labeled Prostaglandin F1β.

HY-W701060

2-Amino-3-Methylimidazo[4,5-f]quinoxaline-d3
2-Amino-3-Methylimidazo[4,5-f]quinoxaline-d₃ is the deuterium labeled 2-Amino-3-Methylimidazo[4,5-f]quinoxaline (HY-W585908).

HY-W281364S

2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine-13C
2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine- ¹³C is the ¹³C-labeled 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine (HY-W281364). 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine is a mutagenic compound .

HY-W014901S1

Bisphenol F-13C12

Bisphenol F- ¹³C₁₂ is the ¹³C labeled Bisphenol F (HY-W014901). Bisphenol F is an orally active endocrine disruptor. Bisphenol F promotes ROS generation, upregulates p-AKT/p-GSK3β, and induces Apoptosis. Bisphenol F interferes with glucose metabolism, affects neurodevelopment and reproductive function. Bisphenol F reduces social novelty preference in mouse offspring. Bisphenol F can be used in bone, blood, and fat-related studies. Bisphenol F is used as a substitute for Bisphenol A (HY-18260) .

HY-W014901S

Bisphenol F-13C6

Bisphenol F- ¹³C₆ is the ¹³C labeled Bisphenol F (HY-W014901). Bisphenol F is an orally active endocrine disruptor. Bisphenol F promotes ROS generation, upregulates p-AKT/p-GSK3β, and induces Apoptosis. Bisphenol F interferes with glucose metabolism, affects neurodevelopment and reproductive function. Bisphenol F reduces social novelty preference in mouse offspring. Bisphenol F can be used in bone, blood, and fat-related studies. Bisphenol F is used as a substitute for Bisphenol A (HY-18260) .

HY-W706319

2-Amino-3-methyl-3H-imidazo[4,5-f]quinoline-d3
2-Amino-3-methyl-3H-imidazo[4,5-f]quinoline-d₃ is deuterium labeled 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine. 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine is a mutagenic compound .

HY-W700103

2-Amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline-d3
2-Amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline-d₃ is the deuterium labeled 2-Amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline.

HY-129953S1

9α,11β-Prostaglandin F2α-d9
9α,11β-Prostaglandin F2α-d₉ is the deuterium labeled 9α,11β-Prostaglandin F2α .

HY-W779193

2-Amino-3-methyl-3H-imidazo[4,5-f]quinoline-2-13C
2-Amino-3-methyl-3H-imidazo[4,5-f]quinoline-2- ¹³C is ¹³C labeled 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine. 2-Ammo-3-memyl-imidazo-[4,5-f]-quinoIine is a mutagenic compound .

HY-129953S

9α,11β-Prostaglandin F2α-d4
9α,11β-Prostaglandin F2α-d4 is a deuterated labeled 9α,11β-Prostaglandin F2α . 9α,11β-Prostaglandin F2α is an endogenous metabolite present in Urine that can be used for the research of Asthma .

HY-103447S1

Zearalenone-13C18
Zearalenone- ¹³C₁₈ (Mycotoxin F2- ¹³C₁₈; Toxin F2- ¹³C₁₈) is the ¹³C labeled Zearalenone (HY-103447) . Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs, cattle and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts .

HY-W706161

Kresoxim-methyl-d7
Kresoxim-methyl-d₇ (BAS 490 F-d₇) is deuterium labeled Kresoxim-methyl .

HY-113459S1

13,14-Dihydro-15-keto Prostaglandin F2α-d4
13,14-Dihydro-15-keto Prostaglandin F2α-d4 (13,14-Dihydro-15-keto-PGF2α-d4) is a deuterated labeled 13,14-Dihydro-15-keto Prostaglandin F2α (HY-113208). 13,14-Dihydro-15-keto Prostaglandin F2α-d4 is an endogenous metabolite present in Blood that can be used for the research of Pregnancy .

HY-113209S

8-Iso-PGF2a-d4
8-Iso-PGF2a-d₄ (8-iso Prostaglandin F2α-d₄) is an active compound. 8-Iso-PGF2a-d₄ can be used the internal standard .

HY-13631AS1

Exatecan-d3 mesylate
Exatecan-d₃ (DX8951f-d₃) mesylate is deuterium-labeled Exatecan mesylate (HY-13631A). Exatecan mesylate is a DNA topoisomerase I inhibitor, with an IC₅₀ of 0.975 μg/mL .

HY-134178S1

5-Fluorouridine 5'-triphosphate-13C,19F,d1
5-Fluorouridine 5'-triphosphate- ¹³C, ¹⁹F,d₁ is deuterium and ¹³C-labeled 5-Fluorouridine 5'-triphosphate (HY-134178).

HY-W725077S

Benalaxyl metabolite F4-d9
Benalaxyl metabolite F4-d₉ (Methyl N-(2,6-dimethylphenyl)-N-(formyl)-DL-alaninate-d₉) is deuterium labeled Methyl N-(2,6-dimethylphenyl)-N-formylalaninate .

HY-12956S

Dinoprost-d4
Dinoprost-d₄ is the deuterium labeled Dinoprost. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour .

HY-12956S1

Dinoprost-d9
Dinoprost-d₉ is the deuterium labeled Dinoprost. Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour .

HY-129397S

2,3-Dinor-11β-prostaglandin F2α-d9
2,3-Dinor-11β-prostaglandin F2α-d₉ is the deuterium labeled 2,3-Dinor-11β-prostaglandin F2α .

HY-113208AS1

11β-13,14-Dihydro-15-keto Prostaglandin F2α-d4
11β-13,14-Dihydro-15-keto Prostaglandin F2α-d₄ is is the deuterium labeled 11β-13,14-dihydro-15-keto Prostaglandin F2α.

HY-103447S2

Zearalenone-13C7
Zearalenone- ¹³C₇ (Mycotoxin F2- ¹³C₇) is ¹³C labeled Zearalenone. Zearalenone is a mycotoxin produced mainly by fungi belonging to the genus Fusarium in foods and feeds. Possess oestrogenic activity in pigs, cattle and sheep, with low acute toxicity. Causes precocious development of mammae and other estrogenic effects in young gilts .

HY-12956S2

Dinoprost-13C5
Dinoprost- ¹³C₅ is ¹³C labeled Dinoprost (HY-12956). Dinoprost (Prostaglandin F2α) is an orally active, potent prostaglandin F (PGF) receptor (FP receptor) agonist. Dinoprost is a luteolytic hormone produced locally in the endometrial luminal epithelium and corpus luteum (CL). Dinoprost plays a key role in the onset and progression of labour .

HY-13631AS

Exatecan-d5 mesylate
Exatecan-d₅ (DX8951f-d₅) mesylate is deuterium labeled Exatecan mesylate (HY-13631A). Exatecan mesylate is a DNA topoisomerase I inhibitor, with an IC₅₀ of 2.2 μM (0.975 μg/mL). Exatecan mesylate can be used in cancer research .

HY-12542S

Dantrolene-13C3

Dantrolene- ¹³C₃ is the ¹³C₃ labeled Dantrolene. Dantrolene (F368), a muscle relaxant, non-competitively inhibits human erythrocyte glutathione reductase. Ki and IC50 values are 111.6 μM and 52.3 μM, respectively. Dantrolene is a ryanodine receptor antagonist and Ca2+ signaling stabilizer. Dantrolene can be used for the research of muscle spasticity, malignant hyperthermia, Huntington's disease and other neuroleptic malignant syndrome.

HY-W754764S

11-(4-Nitrosopiperazin-1-yl)dibenzo[b,f][1,4]thiazepine-d8
11-(4-Nitrosopiperazin-1-yl)dibenzo[b,f][1,4]thiazepine-d₈ (Nitroso aryl piperazine-d₈) is deuterium labeled Nitroso aryl piperazine .

HY-114553S

1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid-d5
1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid-d₅ (5F-PB-223-Carboxyindolemetabolite-d₅) is deuterium labeled 1-(5-Fluoropentyl)-1H-indole-3-carboxylic acid .

HY-W128969S

5-Bromo-2,4-di-tert-butoxypyrimidine-13C,15N2
5-Bromo-2,4-di-tert-butoxypyrimidine- ¹³C, ¹⁵N₂ (IFLAB-BB F1371-0151- ¹³C, ¹⁵N₂) is the ¹³C- and ¹⁵N-labeled 5-Bromo-2,4-di-tert-butoxypyrimidine (HY-W128969).

HY-W779191

MeIQx-13C
MeIQx- ¹³C (2-Amino-3,8-dimethylimidazo[4,5-f]quinoxaline-2- ¹³C) is the ¹³C-labeled MeIQx (HY-W355129). MeIQx, a dietary aromatic amine, is mutagenic compound could be isolated from present in fried beef and beef extracts. MeIQx binds covalently to hemoglobin. MeIQx induces liver tumors .

HY-44745S

4-Ethyl-1,4,7,8-tetrahydro-3H,10H-spiro[pyrano[3,4-f]indolizine-6,2'-[1,3]dioxolane]-3,10-dione-d5
4-Ethyl-1,4,7,8-tetrahydro-3H,10H-spiro[pyrano[3,4-f]indolizine-6,2'-[1,3]dioxolane]-3,10-dione-d5 is the deuterium labeled 4-Ethyl-1,4,7,8-tetrahydro-3H,10H-spiro[pyrano[3,4-f]indolizine-6,2'-[1,3]dioxolane]-3,10-dione .

HY-44302S

4'-Ethyl-4'-hydroxy-7',8'-dihydrospiro[[1,3]dioxolane-2,6'-pyrano[3,4-f]indolizine]-3',10'(1'H,4'H)-dione-d5
4'-Ethyl-4'-hydroxy-7',8'-dihydrospiro[[1,3]dioxolane-2,6'-pyrano[3,4-f]indolizine]-3',10'(1'H,4'H)-dione-d₅ is the deuterium labeled 4'-Ethyl-4'-hydroxy-7',8'-dihydrospiro[[1,3]dioxolane-2,6'-pyrano[3,4-f]indolizine]-3',10'(1'H,4'H)-dione .

HY-14648S5

Dexamethasone-d3-1

Dexamethasone-d₃-1 (Hexadecadrol-d₃-1; Prednisolone F-d₃-1) is a deuterium labeled Dexamethasone (HY-14648). Dexamethasone (Hexadecadrol) is a glucocorticoid receptor agonist. Dexamethasone also significantly decreases CD11b, CD18, and CD62L expression on neutrophils, and CD11b and CD18 expression on monocytes. Dexamethasone is highly effective in the control of COVID-19 infection. Dexamethasone inhibits production of exosomes containing inflammatory microRNA-155 in lipopolysaccharide-induced macrophage inflammatory responses.

HY-W011577S1

Dibenzo[a,c]anthracene-13C6

Dibenzo[a,c]anthracene- ¹³C₆ (2,3-Benzotriphenylene- ¹³C₆) is ¹³C labeled Benzo[f]tetraphene. Benzo[f]tetraphene (Dibenz[a,c]anthracene) is a polycyclic aromatic hydrocarbon with significant antitumor activity. Benzo[f]tetraphene is used as a luminescent probe in cell biology research and can effectively detect reactive oxygen species in biological systems. Benzo[f]tetraphene can also be used as a potential photosensitizer and shows good application prospects in photodynamic inhibition.

HY-169326S

JAK2-IN-11
JAK2-IN-11 (Example 6) is a JAK2 kinase inhibitor with IC₅₀ ≤10 nM against JH2 BIND WT/V617F. JAK2-IN-11 has antitumor activity .

HY-13017S2

Ivacaftor-d18
Ivacaftor-d₁₈ is the deuterium labeled Ivacaftor . Ivacaftor (VX-770) is a potent and orally bioavailable CFTR potentiator, targeting G551D-CFTR and F508del-CFTR with EC₅₀s of 100 nM and 25 nM, respectively .

HY-159578S

VU6036864
VU6036864 (compound 45) is an orally active, selective mAChR M5 antagonist with IC₅₀=20 nM for human M5. VU6036864 is >500-fold selective for human M1-4, with BBB characteristic and high oral bioavailability (%F>100%) .

HY-113437AS

1,2-Dipalmitoyl-sn-glycerol 3-phosphate-d62 sodium
1,2-Dipalmitoyl-sn-glycerol 3-phosphate-d₆₂ (sodium) is deuterium labeled 1,2-Dipalmitoyl-sn-glycerol 3-phosphate. 1,2-Dipalmitoyl-sn-glycerol 3-phosphate sodium (compound 3-F7) is a phosphatidic acid and a human endogenous metabolite .

HY-152066S

Chlorprothixene-d3
Chlorprothixene-d₃ is the deuterium labeled Chlorprothixene Ep Impurity F (HY-Z16039).

HY-13017S4

Ivacaftor-13C6
Ivacaftor- ¹³C₆ (VX-770- ¹³C₆) is ¹³C labeled Ivacaftor. Ivacaftor (VX-770) is a potent and orally bioavailable CFTR potentiator, targeting G551D-CFTR and F508del-CFTR with EC₅₀s of 100 nM and 25 nM, respectively.

HY-13017S3

Ivacaftor-d4
Ivacaftor-d4 (VX-770-d4) is the deuterium labeled-Ivacaftor (HY-13017). Ivacaftor is a potent and orally active CFTR potentiator, targeting G551D-CFTR and *F508del-CFTR* with EC₅₀s of 100 nM and 25 nM, respectively .

HY-14881S2

Bedaquiline impurity 2-d6
Bedaquiline impurity 2-d₆ is deuterium labeled Bedaquiline. Bedaquiline (TMC207) is a diarylquinoline agent and inhibits Mycobacterium tuberculosis (Mtb) F1FO-ATP synthase through targeting of both the c- and the ε-subunit . Bedaquiline has uncoupler activity. Bedaquiline is used for the multi-agent resistant tuberculosis .

HY-14881S1

(Rac)-Bedaquiline-d6
(Rac)-Bedaquiline-d₆ is the deuterium labeled Bedaquiline (HY-14881) . Bedaquiline (TMC207) is a diarylquinoline agent and inhibits Mycobacterium tuberculosis (Mtb) F1FO-ATP synthase through targeting of both the c- and the ε-subunit . Bedaquiline has uncoupler activity. Bedaquiline is used for the multi-agent resistant tuberculosis .

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