Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C9H16N4O3 |
| Molecular Weight | 228.2483 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NCC(=O)N1CCC[C@H]1C(=O)NCC(N)=O
InChI
InChIKey=JWWLMJFURJYNEX-LURJTMIESA-N
InChI=1S/C9H16N4O3/c10-4-8(15)13-3-1-2-6(13)9(16)12-5-7(11)14/h6H,1-5,10H2,(H2,11,14)(H,12,16)/t6-/m0/s1
| Molecular Formula | C9H16N4O3 |
| Molecular Weight | 228.2483 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| GPG-NH2 acts via the metabolite alphaHGA to target HIV-1 Env to the ER-associated protein degradation pathway. | 2010-03-15 |
|
| Targeting human immunodeficiency virus type 1 assembly, maturation and budding. | 2007 |
|
| Glycine-amide is an active metabolite of the antiretroviral tripeptide glycyl-prolyl-glycine-amide. | 2005-01 |
|
| Obligatory involvement of CD26/dipeptidyl peptidase IV in the activation of the antiretroviral tripeptide glycylprolylglycinamide (GPG-NH(2)). | 2004-09 |
|
| No cross-resistance or selection of HIV-1 resistant mutants in vitro to the antiretroviral tripeptide glycyl-prolyl-glycine-amide. | 2004-02 |
|
| The tripeptide glycyl-prolyl-glycine amide does not affect the early steps of the human immunodeficiency virus type 1 replication. | 2001-02-24 |
|
| The nontoxic tripeptide glycyl-prolyl-glycine amide inhibits the replication of human immunodeficiency virus type 1. | 2001-02-24 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:59:08 GMT 2025
by
admin
on
Mon Mar 31 21:59:08 GMT 2025
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| Record UNII |
73GV270Z6Z
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| Record Status |
Validated (UNII)
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| Record Version |
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141497-12-3
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100000127613
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456396
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73GV270Z6Z
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SUB33669
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