H-Gly-Pro-Gly-NH2

Name: H-Gly-Pro-Gly-NH2 | 141497-12-3
Brand: US-CATO
SKU: S57CPTD787999_10_MG
Price: 19998.0 USD
Availability: OutOfStock

Cat. No S57CPTD787999_10_MG

Vendor: US-CATO

Product Information

Product Name

H-Gly-Pro-Gly-NH2

Brand Name

US-CATO

Product Number

CPTD787999

CAS

141497-12-3

Certificate of Analysis (COA)

COA not found

General Information

PubChem CID

456396

IUPAC Name

(2S)-1-(2-aminoacetyl)-N-(2-amino-2-oxoethyl)pyrrolidine-2-carboxamide

InChI Key

JWWLMJFURJYNEX-LURJTMIESA-N

SMILES

C1CC@H(N(C1)C(=O)CN)C(=O)NCC(=O)N

References Data Source From Pubchem

Atomic scale insights into urea–peptide interactions in solution

Publication Name: Physical chemistry chemical physics : PCCP

Publication Date: 2016-02-07

DOI: 10.1039/c5cp06646h

Anti-human immunodeficiency virus type 1 agent alpha-hydroxy glycineamide enters the target cells via a mechanism of passive diffusion

Publication Name: The Journal of pharmacy and pharmacology

Publication Date: 2014-10-01

DOI: 10.1111/jphp.12269

GPG-NH2 acts via the metabolite alphaHGA to target HIV-1 Env to the ER-associated protein degradation pathway

Publication Name: Retrovirology

Publication Date: 2010-03-15

DOI: 10.1186/1742-4690-7-20

Isolation and characterization of a small antiretroviral molecule affecting HIV-1 capsid morphology

Publication Name: Retrovirology

Publication Date: 2009-04-08

DOI: 10.1186/1742-4690-6-34

Targeting Human Immunodeficiency Virus Type 1 Assembly, Maturation and Budding

Publication Name: Drug Target Insights

Publication Date: 2007-01

DOI: 10.1177/117739280700200020

H-Gly-Pro-Gly-NH2

Product Information

General Information

References Data Source From Pubchem

Atomic scale insights into urea–peptide interactions in solution

Anti-human immunodeficiency virus type 1 agent alpha-hydroxy glycineamide enters the target cells via a mechanism of passive diffusion

GPG-NH2 acts via the metabolite alphaHGA to target HIV-1 Env to the ER-associated protein degradation pathway

Isolation and characterization of a small antiretroviral molecule affecting HIV-1 capsid morphology

Targeting Human Immunodeficiency Virus Type 1 Assembly, Maturation and Budding

H-Gly-Pro-Gly-NH2

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-Gly-Pro-Gly-NH2

Product Information

General Information

References Data Source From Pubchem

Atomic scale insights into urea–peptide interactions in solution

Anti-human immunodeficiency virus type 1 agent alpha-hydroxy glycineamide enters the target cells via a mechanism of passive diffusion

GPG-NH2 acts via the metabolite alphaHGA to target HIV-1 Env to the ER-associated protein degradation pathway

Isolation and characterization of a small antiretroviral molecule affecting HIV-1 capsid morphology

Targeting Human Immunodeficiency Virus Type 1 Assembly, Maturation and Budding

H-Gly-Pro-Gly-NH2

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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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