H-Asp-Ala-OH

Name: H-Asp-Ala-OH | 13433-02-8
Brand: US-CATO
SKU: S57CPTD787568_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787568_10_MG

Vendor: US-CATO

Product Information

Product Name

H-Asp-Ala-OH

Brand Name

US-CATO

Product Number

CPTD787568

CAS

13433-02-8

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

5491963

IUPAC Name

(3S)-3-amino-4-(1S)-1-carboxyethylamino-4-oxobutanoic acid

InChI Key

DVUFTQLHHHJEMK-IMJSIDKUSA-N

SMILES

CC@@H(C(=O)O)NC(=O)C@H(CC(=O)O)N

References Data Source From Pubchem

Functional Characterization of the Lin28/let-7 Circuit During Forelimb Regeneration in Ambystoma mexicanum and Its Influence on Metabolic Reprogramming

Publication Name: Frontiers in Cell and Developmental Biology

Publication Date: 2020-11-19

DOI: 10.3389/fcell.2020.562940

Molecular modeling and dynamics studies with explicit inclusion of electronic polarizability: theory and applications

Publication Name: Theoretical Chemistry Accounts

Publication Date: 2009-08-08

DOI: 10.1007/s00214-009-0617-x

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of β-Lactam Antibiotics and Tripeptides as Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Publication Name: Journal of Medicinal Chemistry

Publication Date: 2005-05-26

DOI: 10.1021/jm048982w

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of Peptide Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Publication Name: Journal of Medicinal Chemistry

Publication Date: 2003-11-14

DOI: 10.1021/jm030976x

Carbonic anhydrase activators: Human isozyme II is strongly activated by oligopeptides incorporating the carboxyterminal sequence of the bicarbonate anion exchanger AE1

Publication Name: Bioorganic & Medicinal Chemistry Letters

Publication Date: 2002-04-22

DOI: 10.1016/s0960-894x(02)00121-x

H-Asp-Ala-OH

Product Information

General Information

References Data Source From Pubchem

Functional Characterization of the Lin28/let-7 Circuit During Forelimb Regeneration in Ambystoma mexicanum and Its Influence on Metabolic Reprogramming

Molecular modeling and dynamics studies with explicit inclusion of electronic polarizability: theory and applications

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of β-Lactam Antibiotics and Tripeptides as Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of Peptide Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Carbonic anhydrase activators: Human isozyme II is strongly activated by oligopeptides incorporating the carboxyterminal sequence of the bicarbonate anion exchanger AE1

H-Asp-Ala-OH

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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H-Asp-Ala-OH

Product Information

General Information

References Data Source From Pubchem

Functional Characterization of the Lin28/let-7 Circuit During Forelimb Regeneration in Ambystoma mexicanum and Its Influence on Metabolic Reprogramming

Molecular modeling and dynamics studies with explicit inclusion of electronic polarizability: theory and applications

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of β-Lactam Antibiotics and Tripeptides as Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Three-Dimensional Quantitative Structure−Activity Relationship Analyses of Peptide Substrates of the Mammalian H+/Peptide Cotransporter PEPT1

Carbonic anhydrase activators: Human isozyme II is strongly activated by oligopeptides incorporating the carboxyterminal sequence of the bicarbonate anion exchanger AE1

H-Asp-Ala-OH

Related Product

Mycophenolate Mofetil EP Impurity H

Mycophenolate Mofetil

Flurbiprofen Impurity 21 (Mixture of Diastereomers)

Docetaxel Impurity 40

H-Met-Glu-OH

Fluticasone Impurity 106

Efavirenz Related Compound C

Cholecalciferol EP Impurity A

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