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Details

Stereochemistry ABSOLUTE
Molecular Formula C48H73ClN2O6
Molecular Weight 809.556
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GSK-2838232

SMILES

[H][C@]12CC[C@]3([H])[C@@]4(C)CC[C@H](OC(=O)CC(C)(C)C(O)=O)C(C)(C)[C@]4([H])CC[C@@]3(C)[C@]1(C)CC[C@]5(CC(=O)C(C(C)C)=C25)[C@@H](O)CN(CCN(C)C)CC6=CC=C(Cl)C=C6

InChI

InChIKey=MEOWKUXNVNJAMY-PZFKGGKESA-N
InChI=1S/C48H73ClN2O6/c1-30(2)40-34(52)26-48(37(53)29-51(25-24-50(10)11)28-31-12-14-32(49)15-13-31)23-22-46(8)33(41(40)48)16-17-36-45(7)20-19-38(57-39(54)27-43(3,4)42(55)56)44(5,6)35(45)18-21-47(36,46)9/h12-15,30,33,35-38,53H,16-29H2,1-11H3,(H,55,56)/t33-,35+,36-,37+,38+,45+,46-,47-,48+/m1/s1

HIDE SMILES / InChI

Approval Year

Patents

Patents

Name Type Language
GSK-2838232
Common Name English
GSK-8232
Code English
28-NORLUP-18-EN-21-ONE, 3-(3-CARBOXY-3-METHYL-1-OXOBUTOXY)-17-((1R)-2-(((4-CHLOROPHENYL)METHYL)(2-(DIMETHYLAMINO)ETHYL)AMINO)-1-HYDROXYETHYL)-, (3.BETA.)-
Systematic Name English
Code System Code Type Description
CAS
1443460-91-0
Created by admin on Sat Dec 16 08:01:24 GMT 2023 , Edited by admin on Sat Dec 16 08:01:24 GMT 2023
PRIMARY
FDA UNII
G9C7884M8M
Created by admin on Sat Dec 16 08:01:24 GMT 2023 , Edited by admin on Sat Dec 16 08:01:24 GMT 2023
PRIMARY
MANUFACTURER PRODUCT INFORMATION
GSK-2838232
Created by admin on Sat Dec 16 08:01:24 GMT 2023 , Edited by admin on Sat Dec 16 08:01:24 GMT 2023
PRIMARY Biological Activity of GSK2838232: GSK2838232 inhibits HIV reverse transcriptase activity across a broad panel of HIV-1 isolates, extracted from patent WO/2013090664A1, compound 51.
PUBCHEM
71580991
Created by admin on Sat Dec 16 08:01:24 GMT 2023 , Edited by admin on Sat Dec 16 08:01:24 GMT 2023
PRIMARY