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Details

Stereochemistry ABSOLUTE
Molecular Formula C18H25AsN4O9S
Molecular Weight 548.399
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-(N-(S-GLUTATHIONYLACETYL)AMINO)PHENYLARSONOUS ACID

SMILES

N[C@@H](CCC(=O)N[C@@H](CSCC(=O)NC1=CC=C(C=C1)[As](O)O)C(=O)NCC(O)=O)C(O)=O

InChI

InChIKey=ADJQAKCDADMLPP-STQMWFEESA-N
InChI=1S/C18H25AsN4O9S/c20-12(18(29)30)5-6-14(24)23-13(17(28)21-7-16(26)27)8-33-9-15(25)22-11-3-1-10(2-4-11)19(31)32/h1-4,12-13,31-32H,5-9,20H2,(H,21,28)(H,22,25)(H,23,24)(H,26,27)(H,29,30)/t12-,13-/m0/s1

HIDE SMILES / InChI
Glutathione arsenoxide (GSAO) is a peptide trivalent arsenical that has potential anti-angiogenic capability, suggesting that it could be used for treatment in cancers where tumor metastasis relies on new blood vessel formation (angiogenesis). Endothelial cell proliferation drives new blood vessel formation. GSAO treatment causes a concentration-dependent increase in superoxide levels, ATP depletion, mitochondrial depolarization, and apoptosis in proliferating, but not endothelial cells. GSAO is able to block blood flow to solid tumors in mice, thereby inhibiting tumor growth in mice with no apparent toxicity at efficacious doses. Initial experiments have implicated GSAO in perturbing mitochondrial function. Other molecular effects of GSAO in human cells, for example on the phosphorylation of proteins, are still largely unknown. A phase I clinical trial has been terminated.

Approval Year

Name Type Language
4-(N-(S-GLUTATHIONYLACETYL)AMINO)PHENYLARSONOUS ACID
Systematic Name English
J2.673.618H
Code English
GLYCINE, L-.GAMMA.-GLUTAMYL-S-(2-((4-(HYDROXYARSINYL)PHENYL)AMINO)-2-OXOETHYL)-L-CYSTEINYL-
Systematic Name English
GSAO
Common Name English
P-GSAO
Common Name English
Code System Code Type Description
CAS
334756-34-2
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY
CAS
1271726-51-2
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
ALTERNATIVE
FDA UNII
DSA0237V7T
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID901047773
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY
SMS_ID
100000175092
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY
CHEBI
50016
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY
PUBCHEM
9893715
Created by admin on Sat Dec 16 01:56:40 GMT 2023 , Edited by admin on Sat Dec 16 01:56:40 GMT 2023
PRIMARY