11

(E/Z)-Mirin

11 Publications Verification

Cat. No.: HY-117693

CAS No.: 299953-00-7

Purity: 98.62%

Target:

ATM/ATR

Research Areas:

Cancer

(E/Z)-Mirin is a mixture of (E)-Mirin and Mirin ((Z)-Mirin) (HY-19959) configurations. Among them, Mirin is an inhibitor of MRN (Mre11-Rad50-Nbs1). Mirin prevents MRN-dependent ATM activation without affecting ATM protein kinase activity .

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8

L-Homocysteine

8 Cited Publications

Cat. No.: HY-W010347

CAS No.: 6027-13-0

Category:

Human Gut Microbiota Metabolites Microorganisms Anti-aging Ketones, Aldehydes, Acids Endogenous metabolite Disease Research Fields Inflammation/Immunology

Target:

Endogenous Metabolite Cathepsin

L-Homocysteine, an amino acid, is a homocysteine that has L configuration. Homocysteine is an essential intermediate in normal mammalian metabolism of methionine. L-Homocysteine induces upregulation of Cathepsin V that mediates vascular endothelial inflammation in hyperhomocysteinaemia .

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2

L-Homocysteine-d4

2 Cited Publications

Cat. No.: HY-W653733

CAS No.: 331665-12-4

L-Homocysteine-d₄ is deuterium labeled L-Homocysteine (HY-W010347) . L-Homocysteine, an amino acid, is a homocysteine that has L configuration. Homocysteine is an essential intermediate in normal mammalian metabolism of methionine. L-Homocysteine induces upregulation of Cathepsin V that mediates vascular endothelial inflammation in hyperhomocysteinaemia

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1

DL-Glyceric Acid (20% in water)

1 Cited Publications

Cat. No.: HY-W018035

CAS No.: 473-81-4

Synonyms: Glyceric Acid (20% in Water,ca.2 mol/L)

Category:

Microorganisms Ketones, Aldehydes, Acids Metabolic Disease Endogenous metabolite Disease Research Fields

Target:

Endogenous Metabolite

DL-Glyceric Acid (20% in water) is a metabolite of plants and mammals and exists in two configurations, D and L .

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1

(S)-2-Hydroxy-3-phenylpropanoic acid

1 Cited Publications

Cat. No.: HY-30220

CAS No.: 20312-36-1

Synonyms: L-(-)-3-Phenyllactic Acid

Category:

Ketones, Aldehydes, Acids Metabolic Disease Endogenous metabolite Disease Research Fields

Target:

Endogenous Metabolite Fungal

(S)-2-Hydroxy-3-phenylpropanoic acid is the L-configuration of 2-Hydroxy-3-phenylpropanoic acid, and its level is closely related to some diseases, such as phenylketonuria .

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1

Clevudine

1 Cited Publications

Cat. No.: HY-13859

CAS No.: 163252-36-6

Purity: 99.93%

Synonyms: L-FMAU

Target:

HBV DNA/RNA Synthesis Orthopoxvirus

Research Areas:

Infection

Clevudine (L-FMAU), a nucleoside analog of the unnatural L-configuration, has potent anti-HBV activity with long half-life, low toxicity. Clevudine is a non-competitive inhibitor that is not incorporated into the viral DNA but rather binds to the polymerase. Clevudine is active against cowpox virus respiratory infection in mice .

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1

(rel)-PROTAC ERRα Degrader-1

1 Cited Publications

Cat. No.: HY-128838A

Purity: 98.18%

Target:

PROTACs Estrogen Receptor/ERR

Research Areas:

Others

(rel)-PROTAC ERRα Degrader-1 is a relative configuration of PROTAC ERRα Degrader-1. PROTAC ERRα Degrader-1 comprises a MDM2 ligand binding group, a linker and an estrogen-related receptor alpha (ERRa) binding group. PROTAC ERRα Degrader-1 is an estrogen-related receptor alpha (ERRa) degrader .

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1

Fmoc-His(Trt)-OH

1 Cited Publications

Cat. No.: HY-W010712

CAS No.: 109425-51-6

Target:

Amino Acid Derivatives

Research Areas:

Others

Fmoc-His(Trt)-OH is a histidine derivative with a trityl (Trt) group protecting the His side chain. Fmoc-His(Trt)-OH also has an Fmoc group protecting the α-NH₂ group. Fmoc-His(Trt)-OH can be used in solid-phase peptide synthesis to prevent racemization and byproduct formation. Fmoc-His(Trt)-OH acts as a protected histidine precursor in solid-phase peptide synthesis (SPPS), participating in peptide chain construction through amide bond formation. Fmoc-His(Trt)-OH can be precisely incorporated into the target peptide sequence, ensuring correct peptide chain synthesis and reducing impurity formation. Fmoc-His(Trt)-OH is mainly used in the solid-phase synthesis research of pharmaceutical peptides and bioactive peptides, and is particularly suitable for the preparation of peptide drugs requiring precise control of histidine configuration .

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