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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H15N5O5.ClH
Molecular Weight 345.739
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SANGIVAMYCIN MONOHYDROCHLORIDE

SMILES

Cl.NC(=O)C1=CN([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)C3=C1C(N)=NC=N3

InChI

InChIKey=WTSGTUMQZSEZIW-CCUUNMJDSA-N
InChI=1S/C12H15N5O5.ClH/c13-9-6-4(10(14)21)1-17(11(6)16-3-15-9)12-8(20)7(19)5(2-18)22-12;/h1,3,5,7-8,12,18-20H,2H2,(H2,14,21)(H2,13,15,16);1H/t5-,7-,8-,12-;/m1./s1

HIDE SMILES / InChI

Molecular Formula C12H15N5O5
Molecular Weight 309.278
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 4 / 4
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
11.0 µM [Ki]
PubMed

PubMed

TitleDatePubMed
Sangivamycin, a nucleoside analogue, is a potent inhibitor of protein kinase C.
1988 Feb 5
Inhibition of tumor angiogenesis by targeting endothelial surface ATP synthase with sangivamycin.
2007 Nov
Sangivamycin induces apoptosis by suppressing Erk signaling in primary effusion lymphoma cells.
2014 Feb 7
Substance Class Chemical
Created
by admin
on Sat Dec 16 15:07:39 GMT 2023
Edited
by admin
on Sat Dec 16 15:07:39 GMT 2023
Record UNII
B1NYI0L8FN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SANGIVAMYCIN MONOHYDROCHLORIDE
Common Name English
7H-PYRROLO(2,3-D)PYRIMIDINE-5-CARBOXAMIDE, 4-AMINO-7-.BETA.-D-RIBOFURANOSYL-, MONOHYDROCHLORIDE
Systematic Name English
SANGIVAMYCIN HYDROCHLORIDE
Common Name English
NSC-143648
Code English
Classification Tree Code System Code
NCI_THESAURUS C259
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
NCI_THESAURUS C2089
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID20417691
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY
NSC
143648
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY
PUBCHEM
21159376
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY
NCI_THESAURUS
C29417
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY NCIT
CAS
21090-35-7
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY
FDA UNII
B1NYI0L8FN
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
PRIMARY
CAS
1405-48-7
Created by admin on Sat Dec 16 15:07:40 GMT 2023 , Edited by admin on Sat Dec 16 15:07:40 GMT 2023
SUPERSEDED
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