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Isoforms Recommended:	Adenosine A₁ receptor (A₁R)

Results for "

A1

" in MedChemExpress (MCE) Product Catalog:

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Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-147544

A1AR antagonist 5	Adenosine Receptor	Neurological Disease
A1AR antagonist 5 (compound 20) is a potent and selective *A1AR* (A1 adenosine receptor) antagonist, with a pIC₅₀ of 5.83 and a pK_i of 6.11 ^[1].

HY-147543

A1AR antagonist 4	Adenosine Receptor	Neurological Disease
A1AR antagonist 4 (compound 22) is a potent and selective *A1AR* (A1 adenosine receptor) antagonist, with a pIC₅₀ of 5.51 and a pK_i of 6.29 ^[1].

HY-147545

A1AR antagonist 6	Adenosine Receptor	Neurological Disease
A1AR antagonist 6 (compound 15) is a potent and selective *A1AR* (A1 adenosine receptor) antagonist, with a pIC₅₀ of 6.38 and a pK_i of 7.13 ^[1].

HY-144115

A1AR antagonist 1	Adenosine Receptor	Neurological Disease
A1AR antagonist 1 (compound 18g) is a potent A₁ adenosine receptor (AR) antagonist with K_is of 2.08, 6.91, and 31.2 nM for hA1, hA2A and hA2B, respectively ^[1].

HY-144116

A1AR antagonist 2	Adenosine Receptor	Neurological Disease
A1AR antagonist 2 (compound 18h) is a potent A₁ adenosine receptor (AR) antagonist with K_is of 1.49, 10.2, and 50.1 nM for hA₁, hA_2A and hA_2B, respectively ^[1].

HY-146478

A1/A3 AR antagonist 1	Adenosine Receptor	Neurological Disease Inflammation/Immunology
A1/A3 AR antagonist 1 (compound 10) is a potent adenosine 1 (A1) and adenosine 3 (A3) receptor dual antagonist with K_is of 36.7 nM, 25.4 nM and 1.47 nM for human A1, human A3 and rat A1, respectively. A1/A3 AR antagonist 1 can be used for researching kidney failure, inflammatory pulmonary diseases, and Alzheimer’s disease ^[1].

HY-146456

A1AR antagonist 3	Adenosine Receptor	Neurological Disease
A1AR antagonist 3 (compound 13) is a selective adenosine 1 (A1) receptor antagonist with K_is of 9.69 nM and 0.529 nM for human A1 and rat A1, respectively. A1AR antagonist 3 can be used for researching neurological diseases ^[1].

HY-153333

A1/A3 AR antagonist 3	Adenosine Receptor	Cardiovascular Disease
A1/A3 AR antagonist 3 is an *A₁R/A₃R* dual antagonist with high affinity at low-micromolar to low-nanomolar. A1/A3 AR antagonist 3 can be used for the research of chronic heart diseases ^[1].

HY-146479

A1/A3 AR antagonist 2	Adenosine Receptor	Inflammation/Immunology
The compound is an a1/a3 adenosine receptor antagonist, which helps to research (neurological) inflammatory diseases.

HY-119889

A1B11	Sirtuin	Neurological Disease
A1B11 is a selective SIRT inhibitor (SIRT2:IC50=5.3 μM) that can be used in the study of neurodegenerative diseases ^[1].

HY-134863

A1AT modulator 2	Serpin	Infection Inflammation/Immunology
A1AT modulator 2 (compound 33) is a modulator of A1AT (α-1 antitrypsin) with an IC₅₀ value of ＞1.0 μM and an EC₅₀ value of ＜0.4 μM. A1AT modulator 2 can be used for the research of infection and inflammation ^[1].

HY-134858

A1AT modulator 1	Serpin	Others
A1AT modulator 1 is a potent inhibitor of Z ai-antitrypsin polymerisation with a pIC₅₀ value of 8.3 ^[1].

HY-RS18598

A1bg Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
A1bg Mouse Pre-designed siRNA Set A contains three designed siRNAs for A1bg gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

A1bg Mouse Pre-designed siRNA Set A A1bg Mouse Pre-designed siRNA Set A

HY-RS25083

A1bg Rat Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
A1bg Rat Pre-designed siRNA Set A contains three designed siRNAs for A1bg gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

A1bg Rat Pre-designed siRNA Set A A1bg Rat Pre-designed siRNA Set A

HY-RS00009

A1CF Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
A1CF Human Pre-designed siRNA Set A contains three designed siRNAs for A1CF gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

A1CF Human Pre-designed siRNA Set A A1CF Human Pre-designed siRNA Set A

HY-RS00008

A1BG Human Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
A1BG Human Pre-designed siRNA Set A contains three designed siRNAs for A1BG gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

A1BG Human Pre-designed siRNA Set A A1BG Human Pre-designed siRNA Set A

HY-RS22090

A1cf Mouse Pre-designed siRNA Set A	Small Interfering RNA (siRNA)	Others
A1cf Mouse Pre-designed siRNA Set A contains three designed siRNAs for A1cf gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

A1cf Mouse Pre-designed siRNA Set A A1cf Mouse Pre-designed siRNA Set A

HY-135077

Prostaglandin A1 ethyl ester	Drug Intermediate	Others
Prostaglandin A1 ethyl ester is a prodrug form of Prostaglandin A1. Prostaglandin A1 inhibits the activation of platelets ^[1].

HY-N15337

Vineomycin A1 OS-4742 A1	Antibiotic Bacterial	Infection Cancer
Vineomycin A1 (OS-4742 A1) is an antibiotic against Gram-positive bacteria, which is found in Streptomyces matensis subsp. vineus. Vineomycin A1 also shows antitumor activity in mice. Vineomycin A1 is promising for research of skin fibrosis ^[1].

HY-N2344

Procyanidin A1 1 Publications Verification Proanthocyanidin A1	PKC	Inflammation/Immunology
Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca ²⁺ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects ^[1].

HY-N14274

Miyakamide A1	Antibiotic Bacterial	Infection Cancer
Miyakamide A1 is an antibiotic with insecticidal effect. Miyakamide A1 inhibits the growth of Artemia salina. Miyakamide A1 has a weak antixanthomonas activity. Miyakamide A1 inhibits P388 cells with an IC₅₀ of 10.5 μg/mL ^[1].

HY-N14601

Respinomycin A1	Bacterial	Cancer
Respinomycin A1 is an antibiotic. Respinomycin A1 can be found in Streptomyces sp. RK-483. Respinomycin A1 causes the differentiation of leukemic K-562 cells ^[1].

HY-N7452

Coumermycin A1 10+ Cited Publications	JAK Bacterial Orthopoxvirus	Metabolic Disease
Coumermycin A1 is a JAK2 signal activator. Coumermycin A1 inhibits DNA Gyrase which thereby inhibits cell division in bacteria. Coumermycin A1 shows anti-orthopoxvirus activity.

HY-125560

Leucomycin A1	Endogenous Metabolite Antibiotic	Infection
Leucomycin A1 is a main component of the leucomycin complex produced by Streptomyces kitasatoensis, Leucomycin A1 is an antibiotic ^[1].

HY-123121

Nargenicin A1	Antibiotic Apoptosis Bacterial NF-κB	Infection Inflammation/Immunology Cancer
Nargenicin A1 is an antibiotic agent against various Gram-positive bacteria. Nargenicin A1 shows anti-inflammatory activity. Nargenicin A1 protects HINAE cells against Tacrolimus (HY-13756)-induced DNA damage and apoptosis. Nargenicin A1 can also be used for the research of acute myeloid leukemia ^[1].

HY-N7443R

Gibberellin A1 (Standard)	Phytohormone	Others
Gibberellin A1 (Standard) is the analytical standard of Gibberellin A1. This product is intended for research and analytical applications. Gibberellin A1 is a kind of plant hormones. Gibberellin A1 is a growth-promoting acids isolated from immature seed of Phaseolus multiflorus ^[1].

HY-N7443

Gibberellin A1	Phytohormone	Others
Gibberellin A1 is a kind of plant hormones. Gibberellin A1 is a growth-promoting acids isolated from immature seed of Phaseolus multiflorus ^[1].

HY-N2344R

Procyanidin A1 (Standard)	PKC	Inflammation/Immunology
Procyanidin A1 (Standard) is the analytical standard of Procyanidin A1. This product is intended for research and analytical applications. Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca2+ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects ^[1].

HY-163899

(+)-Crinatusin A1	Phosphatase	Metabolic Disease
(+)-Crinatusin A1 (Compound (+)- 4) is a chalcone-monoterpene hybrid, which can be isolated from Cleistocalyx operculatus. (+)-Crinatusin A1 is an inhibitor for protein tyrosine phosphatase 1B (PTP1B) with IC₅₀ of 0.9 μM. (+)-Crinatusin A1 exhibits potential as an antidiabetic agent ^[1].

HY-16147

Combretastatin A1 phosphate Oxi4503; CA1P; Combretastatin A1 diphosphate	Others	Cancer
Combretastatin A1 phosphate (Oxi4503; CA1P; Combretastatin A1 diphosphate) is a potent vascular disruptive agent. Combretastatin A1 phosphate exerts anti-angiogenic effects on tumors. Combretastatin A1 phosphate has the potential for the research of pancreatic neuroendocrine tumors ^[1] .

HY-P2569

Malformin A1	Apoptosis	Cancer
Malformin A1, a cyclic pentapeptide isolated from Aspergillus niger, possess a range of bioactive properties including antibacterial activity. Malformin A1 shows potent cytotoxic activities on human colorectal cancer cells. Malformin A1 induces apoptosis by activating PARP, caspase 3, -7, and -9 ^[1].

HY-105237

Eesperamicin A1	Antibiotic DNA/RNA Synthesis	Cancer
Esperamicin A1, as an extremely potent antitumor antibiotic, is isolated from cultures of Actinomadura verrucosospora. Esperamicin A1 can be used for the research of antitumor ^[1]. Eesperamicin A1 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-N14268

Ezomycin A1	Antibiotic Fungal	Infection
Ezomycin A1 is an antifungal antibiotic. Ezomycin A1 is mainly active against phytopathogens such as Sclerotinia sclerotiorum and Botrytis, and has a control effect on Sclerotinia, Botrytis and Candidiasis of crops ^[1].

HY-N14737

Dunaimycin A1	Fungal	Infection Inflammation/Immunology
Dunaimycin A1 is a 24-membered macrolide compound with immunosuppressive activity and antifungal activity against Aspergillus niger. Dunaimycin A1 is promising for research of autoimmune diseases ^[1].

HY-N7480A

Quinolactacin A1	Cholinesterase (ChE)	Neurological Disease
Quinolactacin A1 is a potent acetylcholinesterase (AChE) inhibitor from solid state fermentation of Penicillium citrinum 90648. Quinolactacin A1 can be used for the research of Alzheimer disease ^[1].

HY-N6704

Enniatin A1	ERK Apoptosis	Cancer
Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC₅₀ of 49 μM in rat liver microsomes ^[1].

HY-N0258R

Epimedin A1 (Standard)	Others	Cancer
Epimedin A1 (Standard) is the analytical standard of Epimedin A1. This product is intended for research and analytical applications. Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.

HY-N14692

Pluracidomycin A1	Antibiotic Bacterial	Infection
Pluracidomycin A1 is a carbapenem antibiotic . Pluracidomycin A1 has anti-Gram-positive bacteria and Gram-negative bacteria activity, and has the effect of inhibiting β-lactamase ^[1].

HY-N13973

Baumycin A1	Antibiotic Bacterial	Infection Cancer
Baumycin A1 is an antitumor antibiotic ^[1].

HY-125738

Obscurolide A1	Phosphodiesterase (PDE)	Neurological Disease Inflammation/Immunology
Obscurolide A1 is a Phosphodiesterase (PDE) inhibitor (IC₅₀=8 mM) that can be obtained from Streptomyces viridochromogenes culture. Obscurolide A1 has the potential to study neurological and inflammatory diseases ^[1].

HY-N14859

4-Hydroxybaumycinol A1	Antibiotic Bacterial	Infection
4-Hydroxybaumycinol A1 is an anthracycline antibiotic. 4-Hydroxybaumycinol A1 has anti-tumor activity ^[1].

HY-113053

Prostaglandin A1	Endogenous Metabolite Apoptosis	Neurological Disease Inflammation/Immunology Endocrinology Cancer
Prostaglandin A1 is a dehydration derivate of Prostaglandin E1. Prostaglandin A1 exhibits inhibitory activities against tumor growth, inflammation, virus replication, platelet aggregation and excitotoxin-induced neurons apoptosis ^[1].

HY-N14138

Diolmycin A1	Antibiotic Parasite	Infection
Diolmycin A1 is an antibiotic with anticoccidial activity ^[1].

HY-N13870

Saquayamycin A1	Bacterial	Infection Cancer
Saquayamycin A1 has antimicrobial effect, but it has weaker effect against Gram-negative bacteria. Saquayamycin A1 has inhibitory effect on leukemia P388 cells and Adriamycin-resistant P388 cells ^[1].

HY-N6950R

Hederacolchiside A1 (Standard)	PI3K Akt mTOR Parasite Apoptosis	Infection Cancer
Hederacolchiside A1 (Standard) is the analytical standard of Hederacolchiside A1. This product is intended for research and analytical applications. Hederacolchiside A1, isolated from Pulsatilla chinensis, suppresses proliferation of tumor cells by inducing apoptosis through modulating PI3K/Akt/mTOR signaling pathway ^[1]. Hederacolchiside A1 has antischistosomal activity, affecting parasite viability both in vivo and in vitro .

HY-N4133

Ciwujianoside A1	Others	Others
Ciwujianoside A1 is isolated from the Eleutherococcus senticosus leaf ^[1].

HY-136871

Decarestrictin A1	Endogenous Metabolite	Infection
Decarestrictine A1 is a fungal metabolite that has been found in Penicillium.

HY-N13952

Arylomycin A1	Antibiotic Bacterial	Infection
Arylomycin A1 is a lipohexapeptide antibiotic against Gram-positive bacteria ^[1].

HY-159666

Nystatin A1	Antibiotic Fungal	Infection
Nystatin A1 is a polyene macrolide antifungal antibiotic that can be isolated from Streptomyces noursei. Nystatin A1 binds to ergosterol on the fungal cell membrane, increasing the permeability of the cell membrane and causing leakage of cell contents, thereby inhibiting the growth and reproduction of fungi ^[1].

HY-N2264

Wulignan A1	Influenza Virus	Infection
Wulignan A1 is isolated from the stems of Schisandra henryi. Wulignan A1 exhibits anti-influenza virus *H1N1* and *H1N1-TR* (a Tamiflu agent resistant virus strain) activities ^[1].

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-N2344

Procyanidin A1 1 Publications Verification Proanthocyanidin A1	Structural Classification Classification of Application Fields Source classification Plants Flavonoids other families Functional Molecules Research of Health Products Phenols Polyphenols Biflavones Inflammation/Immunology Disease Research Fields	PKC
Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca ²⁺ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects ^[1].

HY-N7452

Coumermycin A1 10+ Cited Publications	Structural Classification Microorganisms Antibiotics Source classification	JAK Bacterial Orthopoxvirus
Coumermycin A1 is a JAK2 signal activator. Coumermycin A1 inhibits DNA Gyrase which thereby inhibits cell division in bacteria. Coumermycin A1 shows anti-orthopoxvirus activity.

HY-N7443

Gibberellin A1	Structural Classification Human Gut Microbiota Metabolites Microorganisms Classification of Application Fields Leguminosae Ketones, Aldehydes, Acids Source classification Other Diseases Plants Phaseolus vulgaris Linn. Endogenous metabolite Disease Research Fields	Phytohormone
Gibberellin A1 is a kind of plant hormones. Gibberellin A1 is a growth-promoting acids isolated from immature seed of Phaseolus multiflorus ^[1].

HY-N15337

Vineomycin A1 OS-4742 A1	Structural Classification Microorganisms Antibiotics Source classification	Antibiotic Bacterial
Vineomycin A1 (OS-4742 A1) is an antibiotic against Gram-positive bacteria, which is found in Streptomyces matensis subsp. vineus. Vineomycin A1 also shows antitumor activity in mice. Vineomycin A1 is promising for research of skin fibrosis ^[1].

HY-N14274

Miyakamide A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Miyakamide A1 is an antibiotic with insecticidal effect. Miyakamide A1 inhibits the growth of Artemia salina. Miyakamide A1 has a weak antixanthomonas activity. Miyakamide A1 inhibits P388 cells with an IC₅₀ of 10.5 μg/mL ^[1].

HY-N14601

Respinomycin A1	Structural Classification Natural Products Microorganisms Source classification	Bacterial
Respinomycin A1 is an antibiotic. Respinomycin A1 can be found in Streptomyces sp. RK-483. Respinomycin A1 causes the differentiation of leukemic K-562 cells ^[1].

HY-125560

Leucomycin A1	Infection Structural Classification Microorganisms Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Disease Research Fields	Endogenous Metabolite Antibiotic
Leucomycin A1 is a main component of the leucomycin complex produced by Streptomyces kitasatoensis, Leucomycin A1 is an antibiotic ^[1].

HY-123121

Nargenicin A1	Infection Structural Classification Microorganisms Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Inflammation/Immunology Disease Research Fields Cancer	Antibiotic Apoptosis Bacterial NF-κB
Nargenicin A1 is an antibiotic agent against various Gram-positive bacteria. Nargenicin A1 shows anti-inflammatory activity. Nargenicin A1 protects HINAE cells against Tacrolimus (HY-13756)-induced DNA damage and apoptosis. Nargenicin A1 can also be used for the research of acute myeloid leukemia ^[1].

HY-N7443R

Gibberellin A1 (Standard)	Structural Classification Human Gut Microbiota Metabolites Microorganisms Leguminosae Ketones, Aldehydes, Acids Source classification Plants Phaseolus vulgaris Linn. Endogenous metabolite	Phytohormone
Gibberellin A1 (Standard) is the analytical standard of Gibberellin A1. This product is intended for research and analytical applications. Gibberellin A1 is a kind of plant hormones. Gibberellin A1 is a growth-promoting acids isolated from immature seed of Phaseolus multiflorus ^[1].

HY-N2344R

Procyanidin A1 (Standard)	Structural Classification Flavonoids other families Source classification Phenols Polyphenols Plants Biflavones	PKC
Procyanidin A1 (Standard) is the analytical standard of Procyanidin A1. This product is intended for research and analytical applications. Procyanidin A1 (Proanthocyanidin A1) is a procyanidin dimer, which inhibits degranulation downstream of protein kinase C activation or Ca2+ influx from an internal store in RBL-213 cells. Procyanidin A1 has antiallergic effects ^[1].

HY-163899

(+)-Crinatusin A1	Structural Classification Other Monoterpenes Terpenoids Source classification Myrtaceae Plants Syzygium nervosum Candolle	Phosphatase
(+)-Crinatusin A1 (Compound (+)- 4) is a chalcone-monoterpene hybrid, which can be isolated from Cleistocalyx operculatus. (+)-Crinatusin A1 is an inhibitor for protein tyrosine phosphatase 1B (PTP1B) with IC₅₀ of 0.9 μM. (+)-Crinatusin A1 exhibits potential as an antidiabetic agent ^[1].

HY-P2569

Malformin A1	Natural Products Human Gut Microbiota Metabolites Microorganisms Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields Cancer	Apoptosis
Malformin A1, a cyclic pentapeptide isolated from Aspergillus niger, possess a range of bioactive properties including antibacterial activity. Malformin A1 shows potent cytotoxic activities on human colorectal cancer cells. Malformin A1 induces apoptosis by activating PARP, caspase 3, -7, and -9 ^[1].

HY-N14268

Ezomycin A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Fungal
Ezomycin A1 is an antifungal antibiotic. Ezomycin A1 is mainly active against phytopathogens such as Sclerotinia sclerotiorum and Botrytis, and has a control effect on Sclerotinia, Botrytis and Candidiasis of crops ^[1].

HY-N14737

Dunaimycin A1	Structural Classification Natural Products Microorganisms Source classification	Fungal
Dunaimycin A1 is a 24-membered macrolide compound with immunosuppressive activity and antifungal activity against Aspergillus niger. Dunaimycin A1 is promising for research of autoimmune diseases ^[1].

HY-N7480A

Quinolactacin A1	Alkaloids Microorganisms Pyrrole Alkaloids Classification of Application Fields Neurological Disease Source classification Quinoline Alkaloids Disease Research Fields	Cholinesterase (ChE)
Quinolactacin A1 is a potent acetylcholinesterase (AChE) inhibitor from solid state fermentation of Penicillium citrinum 90648. Quinolactacin A1 can be used for the research of Alzheimer disease ^[1].

HY-N6704

Enniatin A1	Structural Classification Microorganisms Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Antibacterial Disease Research Anticancer Disease Research Fields Cancer	ERK Apoptosis
Enniatin A1 isolated from Fusarium mycotoxins is a cyclic hexadepsipeptide consisting of alternating D-α-hydroxyisovaleric acids and N-methyl-L-amino acids. Enniatin A1 possesses anticarcinogenic properties by induction of apoptosis and disruption of ERK signalling pathway. Enniatin A1 inhibits ACAT with an IC₅₀ of 49 μM in rat liver microsomes ^[1].

HY-N0258R

Epimedin A1 (Standard)	Flavonols Structural Classification Monophenols Flavonoids Source classification Phenols Epimedium brevicornu Maxim. Plants Berberidaceae	Others
Epimedin A1 (Standard) is the analytical standard of Epimedin A1. This product is intended for research and analytical applications. Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.

HY-N14692

Pluracidomycin A1	Structural Classification Natural Products Microorganisms Source classification	Antibiotic Bacterial
Pluracidomycin A1 is a carbapenem antibiotic . Pluracidomycin A1 has anti-Gram-positive bacteria and Gram-negative bacteria activity, and has the effect of inhibiting β-lactamase ^[1].

HY-N13973

Baumycin A1	Quinones Structural Classification Microorganisms Anthraquinones Source classification	Antibiotic Bacterial
Baumycin A1 is an antitumor antibiotic ^[1].

HY-125738

Obscurolide A1	Structural Classification Microorganisms Ketones, Aldehydes, Acids Source classification	Phosphodiesterase (PDE)
Obscurolide A1 is a Phosphodiesterase (PDE) inhibitor (IC₅₀=8 mM) that can be obtained from Streptomyces viridochromogenes culture. Obscurolide A1 has the potential to study neurological and inflammatory diseases ^[1].

HY-N14859

4-Hydroxybaumycinol A1	Structural Classification Natural Products Microorganisms Source classification	Antibiotic Bacterial
4-Hydroxybaumycinol A1 is an anthracycline antibiotic. 4-Hydroxybaumycinol A1 has anti-tumor activity ^[1].

HY-113053

Prostaglandin A1	Structural Classification Animals Ketones, Aldehydes, Acids Source classification	Endogenous Metabolite Apoptosis
Prostaglandin A1 is a dehydration derivate of Prostaglandin E1. Prostaglandin A1 exhibits inhibitory activities against tumor growth, inflammation, virus replication, platelet aggregation and excitotoxin-induced neurons apoptosis ^[1].

HY-N14138

Diolmycin A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Parasite
Diolmycin A1 is an antibiotic with anticoccidial activity ^[1].

HY-N13870

Saquayamycin A1	Structural Classification Microorganisms Antibiotics Source classification	Bacterial
Saquayamycin A1 has antimicrobial effect, but it has weaker effect against Gram-negative bacteria. Saquayamycin A1 has inhibitory effect on leukemia P388 cells and Adriamycin-resistant P388 cells ^[1].

HY-N6950R

Hederacolchiside A1 (Standard)	Triterpenes Structural Classification other families Terpenoids Source classification Plants	PI3K Akt mTOR Parasite Apoptosis
Hederacolchiside A1 (Standard) is the analytical standard of Hederacolchiside A1. This product is intended for research and analytical applications. Hederacolchiside A1, isolated from Pulsatilla chinensis, suppresses proliferation of tumor cells by inducing apoptosis through modulating PI3K/Akt/mTOR signaling pathway ^[1]. Hederacolchiside A1 has antischistosomal activity, affecting parasite viability both in vivo and in vitro .

HY-N13952

Arylomycin A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Arylomycin A1 is a lipohexapeptide antibiotic against Gram-positive bacteria ^[1].

HY-N2264

Wulignan A1	Infection Structural Classification Classification of Application Fields Source classification Lignans Phenols Polyphenols Phenylpropanoids Plants Schisandraceae Schisandra chinensis (Turcz.) Baill. Disease Research Fields	Influenza Virus
Wulignan A1 is isolated from the stems of Schisandra henryi. Wulignan A1 exhibits anti-influenza virus *H1N1* and *H1N1-TR* (a Tamiflu agent resistant virus strain) activities ^[1].

HY-123325

Kapurimycin A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Antibiotic Bacterial
Kapurimycin A1 is an anbitiotic that can be isolated from Streptomyces. Kapurimycin A1 has a significant inhibitory effect on Gram-positive bacteria, exhibits cytotoxicity to cultured mammalian cells, and shows strong antitumor activity against the mouse leukemia P388 cell line ^[1].

HY-N8252

Xanthoquinodin A1	Infection Quinones Microorganisms Classification of Application Fields Source classification Naphthalene Quinones Disease Research Fields	Antibiotic
Xanthoquinodin A1 is an anticoccidial antibiotic having a new xanthone-anthraquinone conjugate system ^[1].

HY-100558

Bafilomycin A1 Maximum Cited Publications 537 Publications Verification BafA1	Infection Structural Classification Microorganisms Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Disease Research Anticancer Disease Research Fields	Proton Pump Autophagy Antibiotic Bacterial Apoptosis
Bafilomycin A1 (BafA1) is a specific and reversible inhibitor of vacuolar H ⁺-ATPase (V-ATPase) with IC₅₀ values of 4-400 nmol/mg. Bafilomycin A1, a macrolide antibiotic, is also used as an autophagy inhibitor at the late stage. Bafilomycin A1 blocks autophagosome-lysosome fusion and inhibits acidification and protein degradation in lysosomes of cultured cells. Bafilomycin A1 induces apoptosis ^[1] .

HY-N6950

Hederacolchiside A1 1 Publications Verification	Infection Triterpenes Structural Classification other families Classification of Application Fields Terpenoids Source classification Plants Disease Research Fields	PI3K Akt mTOR Parasite Apoptosis
Hederacolchiside A1, isolated from Pulsatilla chinensis, suppresses proliferation of tumor cells by inducing apoptosis through modulating PI3K/Akt/mTOR signaling pathway ^[1]. Hederacolchiside A1 has antischistosomal activity, affecting parasite viability both in vivo and in vitro .

HY-N14740

Lanopylin A1	Structural Classification Natural Products Microorganisms Source classification	Others
Lanopylin A1 can inhibit recombinant human lanosterol synthase (EC 5.4.99.7) with an IC₅₀ of 15 μM ^[1].

HY-N14982

Ferrimycin A1	Structural Classification Natural Products Microorganisms Source classification	Antibiotic
Ferrimycin A1 is an iron-containing peptide antibiotic and an acyl derivative of ferrimycin B, a competitive antagonist and microbial growth factor ^[1] .

HY-118834

Teleocidin A1 Lyngbyatoxin A	Alkaloids Microorganisms Classification of Application Fields Source classification Disease Research Fields Indole Alkaloids Cancer	PKC
Teleocidin A1 (Lyngbyatoxin A), a highly toxic skin irritant, is a potent activator of protein kinase C (PKC). Teleocidin A1 shows antiproliferative activity against HeLa cancer cells (IC₅₀=9.2 nM) ^[1] .

HY-N5187

Edeine A1	Structural Classification Microorganisms Antibiotics Source classification Other Antibiotics	Bacterial Fungal
Edeine A1 can inhibit DNA replication and protein biosynthesis, and has anti-Gram-positive bacteria, Gram-negative bacteria, fungi and yeast activities ^[1].

HY-136824

Napyradiomycin A1	Infection Quinones Microorganisms Classification of Application Fields Source classification Naphthalene Quinones Disease Research Fields Cancer	Bacterial Antibiotic
Napyradiomycin A1 is one enantioselective compound of napyradiomycins. napyradiomycins are an intriguing family of halogenated natural products with activity against several tumor cell lines as well as some bacterial strains ^[1].

HY-N6854

Mogroside I A1	Triterpenes Classification of Application Fields Terpenoids Source classification Cucurbitaceae Metabolic Disease Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu et Z. Y. Zhang Plants Disease Research Fields Sweeteners Food Research	Others
Mogroside I A1 is a triterpenoid glycoside and a nonsugar sweetener. Mogrosides are sweeter than sucrose. Mogrosides exhibit antioxidant, antidiabetic and anticancer activities ^[1].

HY-N14127

Cirramycin A1	Structural Classification Microorganisms Macrolide Antibiotics Antibiotics Source classification	Bacterial
Cirramycin A1 has anti-Gram-positive and negative bacterial activity, it is also effective against a variety of mycoplasmas, the minimum inhibitory concentration against Mycoplasmas pneumonia is 0.001 μg/mLs ^[1].

HY-N0258

Epimedin A1 1 Publications Verification Hexandraside F	Flavonols Flavonoids Monophenols Classification of Application Fields Source classification Phenols Epimedium brevicornu Maxim. Plants Berberidaceae Disease Research Fields Cancer	Others
Epimedin A1 is a flavonoid extracted from Herba Epimedii which is one of commonly used Chinese medicines.

HY-N2046

Jujuboside D Jujuboside A1	Triterpenes Classification of Application Fields Ziziphus jujuba Terpenoids Source classification Other Diseases Plants Rhamnaceae Disease Research Fields	Others
Jujuboside D (Jujuboside A1) is a dammarane-type saponin that can be isolated from the seeds of Ziziphus jujube ^[1].

HY-129788

Deltamycin A1	Structural Classification Microorganisms Macrolide Antibiotics Antibiotics Source classification	Antibiotic
Deltamycin A1 is a compound with antibacterial activity. Its structure belongs to the basic macrolide antibiotic family and is different from several other antibiotics of similar structure. Its structure was determined by spectroscopic properties and verified by chemical synthesis.

HY-N11009

11-Oxomogroside II A1	Triterpenes Structural Classification Terpenoids Source classification Cucurbitaceae Siraitia grosvenorii (Swingle) C. Jeffrey ex Lu et Z. Y. Zhang Plants	EBV
11-Oxomogroside II A1 (compound 7) is an oxidized cucurbitin. It can be isolated from the ethanol extract of Rohanberry fruit. 11-Oxomogroside II A1 inhibits the activation of Epstein-Barr virus (EBV) early antigen (EBV-EA) induced by 12-O-tetradecanoylphorbol-13-acetate (TPA). 11-Oxomogroside II A1 also weakly inhibits the activation of (±)-(E)-methyl-2-[(E)-hydroxyimino]-5-nitro-6-methoxy-3-hexemide (NOR 1), a nitric oxide (NO) donor ^[1].

HY-B1342

Vitamin A Vitamin A1; all-trans-Retinol	Structural Classification Natural Products Human Gut Microbiota Metabolites Microorganisms Classification of Application Fields Source classification Metabolic Disease Endogenous metabolite Disease Research Fields	Endogenous Metabolite
Vitamin A (Vitamin A1) is an endogenous metabolite.

HY-N7723

Avenacin A-1	Structural Classification Avena sativa Linn. Terpenoids Gramineae Source classification Plants Pentacyclic Triterpenoids	Fungal Endogenous Metabolite
Avenacin A-1 exhibits antifungal activity, which inhibits growth of Culvularia sp, Drechslera victoriae, Rhizoctonia solani, Fusarium spp.. Avenacin A-1 affects the bilayer permeability ^[1].

HY-N5045

Jionoside A1	Classification of Application Fields Simple Phenylpropanols Source classification Phenols Polyphenols Scrophulariaceae Phenylpropanoids Plants Rehmannia glutinosa (Gaert.) Libosch. ex Fisch. et Mey Disease Research Fields Inflammation/Immunology	Others
Jionoside A1 isolated from Radix Rehmanniae Praeparata displays dose dependent immune-enhancement activity and possesses moderate protective activities on H₂O₂-treated SH-SY5Y cells ^[1].

HY-N6079

Timosaponin A1	Structural Classification Liliaceae Classification of Application Fields Source classification Other Diseases Anemarrhena asphodeloides Bunge Plants Disease Research Fields Steroids	Lipoxygenase Dipeptidyl Peptidase COX
Timosaponin A1, a natural steroidal saponin, is a 5-lipoxygenase (5-LO), COX-2, and dipeptidyl peptidase 4 (DPP-4) inhibitor with IC₅₀s of 3.29 µM, 36.43 µM, and 33.25 µM, respectively ^[1] .

HY-N0541

Pseudoginsenoside F11 1 Publications Verification Ginsenoside A1	Panax ginseng C. A. Meyer Triterpenes Structural Classification Classification of Application Fields Terpenoids Source classification Other Diseases Plants Endogenous metabolite Disease Research Fields Araliaceae	Endogenous Metabolite
Pseudoginsenoside F11 (Ginsenoside A1), a component of Panax quinquefolium (American ginseng), has been demonstrated to antagonize the learning and memory deficits induced by scopolamine, morphine and methamphetamine in mice.

HY-N125722

Venturicidin A Aabomycin A1	Infection Structural Classification Microorganisms Macrolide Antibiotics Classification of Application Fields Antibiotics Source classification Antibacterial Disease Research Disease Research Fields	ATP Synthase Antibiotic
Venturicidin A (Aabomycin A1), from actinomycetes, is a membrane-active natural product inhibitor of ATP synthase. Venturicidin A potentiates the aminoglycoside antibiotic gentamicin against multidrug-resistant clinical isolates of Staphylococcus, Enterococcus, and Pseudomonas aeruginosa. Venturicidin A shows noticeable toxicity toward human embryonic-kidney (HEK)cells with an IC50 of 31 μg/mL.

HY-B1342A

13-cis-Vitamin A 13-cis-Vitamin A1; 13-cis-Retinol	Structural Classification Natural Products Source classification Endogenous metabolite	Drug Isomer Drug Metabolite
13-cis-Vitamin A (13-cis-Vitamin A1) is the 13-cis-isomer of Vitamin A (HY-B1342), which is an active metabolite found in butter ^[1].

HY-118221

Arizonin A1	Quinones Structural Classification Microorganisms Source classification Naphthalene Quinones	Antibiotic Bacterial
Arizonin B1, a microbial metabolite, is an antibiotic with anti-Gram-positive bacterial activities ^[1].

Cat. No.	Product Name	Chemical Structure

HY-B1342S4

Vitamin A-d5
Vitamin A-d5₅ is the deuterium labeled Vitamin A[1].

HY-B1342S2

Vitamin A-d4 1 Publications Verification
Vitamin A-d₄ (Vitamin A1-d₄; all-trans-Retinol-d₄) is the deuterium labeled Vitamin A. Vitamin A is an endogenous metabolite.

HY-B1342S3

Vitamin A-13C3
Vitamin A- ¹³C₃ (Vitamin A1- ¹³C₃; all-trans-Retinol- ¹³C₃) is a ¹³C-labeled Vitamin A/Vitamin A (HY-B1342). Vitamin A is an endogenous metabolite.

HY-B0004S

Doxofylline-d6
Doxofylline-d₆ is the deuterium labeled Doxofylline. Doxofylline is an antagonist of adenosine A1 receptor which also inhibits phosphodiesterase IV.

HY-B1342S5

Vitamin A-d3
Vitamin A-d₃ (Vitamin A1-d₃; all-trans-Retinol-d₃) is a vitamin A analogue ^[1].

HY-142193S

(-)-Erinacin A-d3
(-)-Erinacin A-d₃ is the deuterium labeled (-)-Erinacin A[1].

HY-144221S

Tiotropium bromide EP impurity A-d6
Tiotropium bromide EP impurity A-d₆ is the deuterium labeled Tiotropium bromide EP impurity A[1].

HY-132380S

3-epi-Ochratoxin A-d5
3-epi-Ochratoxin A-d₅ is the deuterium labeled 3-epi-Ochratoxin A[1].

HY-150992S

2,6-Dichloro bisphenol A-d12
2,6-Dichloro bisphenol A-d₁₂ is the deuterium labeled 2,6-Dichloro bisphenol A[1].

HY-150988S

2,2'-Dichloro bisphenol A-d12
2,2'-Dichloro bisphenol A-d₁₂ is the deuterium labeled 2,2'-Dichloro bisphenol A[1].

HY-B0004S1

Doxofylline-d4
Doxofylline-d₄ is the deuterium labeled Doxofylline. Doxofylline is an antagonist of adenosine A1 receptor which also inhibits phosphodiesterase IV[1][2].

HY-150987S

2,2',6-Trichloro bisphenol A-d11
2,2',6-Trichloro bisphenol A-d₁₁ is the deuterium labeled 2,2',6-Trichloro bisphenol A[1].

HY-N0138S1

Theobromine-d3
Theobromine-d₃ is the deuterium labeled Theobromine. Theobromine is a methylxanthine found in cacao beans which can inhibit adenosine receptor A1 (AR1) signaling.

HY-N0138S

Theobromine-d6
Theobromine-d₆ is the deuterium labeled Theobromine. Theobromine is a methylxanthine found in cacao beans which can inhibit adenosine receptor A1 (AR1) signaling.

HY-A0168S

Regadenoson-d3

Regadenoson-d₃ is the deuterium labeled Regadenoson. Regadenoson (CVT-3146) is a potent and selective A2A adenosine receptor agonist, with Kis of 290 and 1120 nM for rat and pig adenosine A2A receptor, respectively. Regadenoson is selective for the adenosine A2A receptor over adenosine A1 and A2B receptors, and shows 13-fold selectivity over the human adenosine A1 receptor. Regadenoson is a vasodilator stress agent has shifted the landscape of vasodilator myocardial perfusion imaging. Regadenoson increases blood-brain barrier (BBB) permeability in rodents[1][2][3].

HY-B0228S8

Adenosine-d1-2
Adenosine-d-2 is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular phys

HY-B0228S7

Adenosine-d1-1
Adenosine-d-1 is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular phys

HY-B0228S6

Adenosine-d2
Adenosine-d₂ is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physio

HY-B0228S5

Adenosine-13C
Adenosine- ¹³C is the ¹³C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology,

HY-B0228S14

Adenosine-d9
Adenosine-d₉ is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physio ^[1] .

HY-B0228S2

Adenosine-2′-13C
Adenosine-2′- ¹³C is the ¹³C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiolo

HY-B0228S3

Adenosine-3′-13C
Adenosine-3′- ¹³C is the ¹³C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiolo

HY-B0228S4

Adenosine-1′-13C
Adenosine-1′- ¹³C is the ¹³C labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiolo

HY-N0092S1

Inosine-13C
Inosine- ¹³C is the ¹³C labeled Inosine. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A₁ (A₁R) and A_2A (A_2AR) receptors ^[1] .

HY-N0092S

Inosine-2,8-d2
Inosine-2,8-d₂ is the deuterium labeled Inosine. Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors ^[1] .

HY-N0092S2

Inosine-13C5
Inosine- ¹³C₅ is the ¹³C₅ labeled Inosine (HY-N0092). Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A₁ (A₁R) and A_2A (A_2AR) receptors ^[1] .

HY-12365S2

Namodenoson-d5
Namodenoson-d₅ (CF-102-d₅) is deuterium labeled Namodenoson. Namodenoson (CF-102) is a selective A3 adenosine receptor (A3AR) agonist (K_i=0.33 nM). Namodenoson displays 2500- and 1400-fold selectivity over A1 and A2A receptors respectively ^[1] .

HY-A0181S1

Adenosine monophosphate-15N5 dilithium
Adenosine monophosphate- ¹⁵N₅ dilithium is the ¹⁵N labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-B0228S

Adenosine-d1
Adenosine-d is the deuterium labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[1][2].

HY-A0181S2

Adenosine monophosphate-d12 dilithium
Adenosine monophosphate-d₁₂ (AMP-d₁₂) dilithium is deuterium labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-18260S4

Bisphenol A-d4

Bisphenol A-d₄ is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].

HY-18260S

Bisphenol A-d16

Bisphenol A-d₁₆ is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].

HY-B0228S1

Adenosine-13C5
Adenosine- ¹³C₅ is the ¹³C labeled Adenosine[1]. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation[2][3].

HY-W779021

Adenosine-15N
Adenosine- ¹⁵N (Adenine riboside- ¹⁵N) is ¹⁵N labeled Adenosine. Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation ^[1] .

HY-18260S5

Bisphenol A-d4-1

Bisphenol A-d₄-1 is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3].

HY-A0181S3

Adenosine monophosphate-13C10 dilithium
Adenosine monophosphate- ¹³C₁₀ (AMP- ¹³C₁₀) dilithium is ¹³C-labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-18260S3

Bisphenol A-d8

Bisphenol A-d₈ is the deuterium labeled Bisphenol A[1]. Bisphenol A is a phenolic, organic synthetic compound widely used in the production of polycarbonate plastics and epoxy resins. Bisphenol A is a reproductive, developmental, and systemic toxicant, often classified as an endocrine-disrupting compound (EDC). Bisphenol A is associated with many diseases, including cardiovascular diseases, respiratory diseases, diabetes, kidney diseases, obesity, and reproductivedisorders[2][3][4].

HY-N0092S3

Inosine-13C10,15N4
Inosine-13C10,15N4 is ¹³C and ¹⁵N labeled Inosine (HY-N0092). Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A₁ (A₁R) and A_2A (A_2AR) receptors ^[1] .

HY-B0228S12

Adenosine-d13

Adenosine-d₁₃ (Adenine riboside-d₁₃; D-Adenosine-d₁₃) is deuterium labeled Adenosine (HY-B0228). Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation.

HY-B0228S13

Adenosine-13C10

Adenosine- ¹³C₁₀ (Adenine riboside- ¹³C₁₀; D-Adenosine- ¹³C₁₀) is ¹³C-labeled Adenosine (HY-B0228). Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation.

HY-A0181BS

Adenosine monophosphate-13C10,15N5 disodium

1 Publications Verification

Adenosine monophosphate- ¹³C₁₀, ¹⁵N₅ (AMP- ¹³C₁₀, ¹⁵N₅) disodium is ¹³C and ¹⁵N-labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-A0181S5

Adenosine monophosphate-15N5,d12 dilithium

Adenosine monophosphate- ¹⁵N₅,d₁₂ (AMP- ¹⁵N₅,d₁₂) dilithium is deuterium and ¹⁵N labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-A0181S

Adenosine monophosphate-13C10,15N5 dilithium

1 Publications Verification

Adenosine monophosphate- ¹³C₁₀, ¹⁵N₅(AMP- ¹³C₁₀, ¹⁵N₅) is the ¹³C-labeled and ¹⁵N-labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-B0228S11

Adenosine-15N5

Adenosine- ¹⁵N₅ (Adenine riboside- ¹⁵N₅; D-Adenosine- ¹⁵N₅) is the ¹⁵N labled Adenosine (HY-B0228). Adenosine (Adenine riboside), a ubiquitous endogenous autacoid, acts through the enrollment of four G protein-coupled receptors: A1, A2A, A2B, and A3. Adenosine affects almost all aspects of cellular physiology, including neuronal activity, vascular function, platelet aggregation, and blood cell regulation ^[1] .

HY-A0181S4

Adenosine monophosphate-13C10,15N5,d12 dilithium

Adenosine monophosphate- ¹³C₁₀, ¹⁵N₅,d₁₂ (AMP- ¹³C₁₀, ¹⁵N₅,d₁₂) dilithium is ¹³C and ¹⁵N-labeled Adenosine monophosphate (HY-A0181). Adenosine monophosphate is an adenosine A1 receptor agonist. Adenosine monophosphate has significant antiviral activity against HSV-1 and HSV-2. Adenosine monophosphate is a key cellular metabolite regulating energy homeostasis and signal transduction ^[1] .

HY-B1342S1

Vitamin A-d6
Vitamin A-d₆ is the deuterium labeled Vitamin A. Vitamin A is an endogenous metabolite.

HY-B1342S

Vitamin A-d8
Vitamin A-d₈ is the deuterium labeled Vitamin A. Vitamin A is an endogenous metabolite.

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