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Details

Stereochemistry ABSOLUTE
Molecular Formula C28H34N2O11
Molecular Weight 574.5764
Optical Activity ( - )
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBOXYSTRICTOSIDINE

SMILES

COC(=O)C1=CO[C@@H](O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](C=C)[C@@H]1C[C@@H]3N[C@@H](CC4=C3NC5=C4C=CC=C5)C(O)=O

InChI

InChIKey=LHKZIVMTXZLOTP-RMKGEEGASA-N
InChI=1S/C28H34N2O11/c1-3-12-14(8-18-21-15(9-19(29-18)25(35)36)13-6-4-5-7-17(13)30-21)16(26(37)38-2)11-39-27(12)41-28-24(34)23(33)22(32)20(10-31)40-28/h3-7,11-12,14,18-20,22-24,27-34H,1,8-10H2,2H3,(H,35,36)/t12-,14+,18+,19+,20-,22-,23+,24-,27+,28+/m1/s1

HIDE SMILES / InChI

Molecular Formula C28H34N2O11
Molecular Weight 574.5764
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 10
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Antimalarial activity and toxicity evaluation of a quantified Nauclea pobeguinii extract.
2010-08-19
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:42:16 GMT 2025
Edited
by admin
on Mon Mar 31 22:42:16 GMT 2025
Record UNII
DD33P75ZZV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(5S)-5-CARBOXYSTRICTOSIDINE
Preferred Name English
CARBOXYSTRICTOSIDINE
Common Name English
1H-PYRIDO(3,4-B)INDOLE-3-CARBOXYLIC ACID, 1-((3-ETHENYL-2-(.BETA.-L-GLUCOPYRANOSYLOXY)-3,4-DIHYDRO-5-(METHOXYCARBONYL)-2H-PYRAN-4-YL)METHYL)-2,3,4,9-TETRAHYDRO-, (2S-(2.ALPHA.,3.BETA.,4.BETA.(1R*,3R*)))-
Systematic Name English
5.BETA.-CARBOXYSTRICTOSIDINE
Common Name English
5-CARBOXYSTRICTOSIDINE
Common Name English
(-)-5-CARBOXYSTRICTOSIDINE
Common Name English
(1S,3S)-1-(((2S,3R,4S)-3-ETHENYL-2-(.BETA.-D-GLUCOPYRANOSYLOXY)-3,4-DIHYDRO-5-(METHOXYCARBONYL)-2H-PYRAN-4-YL)METHYL)-2,3,4,9-TETRAHYDRO-1H-PYRIDO(3,4-B)INDOLE-3-CARBOXYLIC ACID
Systematic Name English
5.BETA.-CARBOXY-3-ISOVINCOSIDE
Common Name English
STRICTOSIDINE, 5.BETA.-CARBOXY-
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID001347342
Created by admin on Mon Mar 31 22:42:16 GMT 2025 , Edited by admin on Mon Mar 31 22:42:16 GMT 2025
PRIMARY
PUBCHEM
10483216
Created by admin on Mon Mar 31 22:42:16 GMT 2025 , Edited by admin on Mon Mar 31 22:42:16 GMT 2025
PRIMARY
FDA UNII
DD33P75ZZV
Created by admin on Mon Mar 31 22:42:16 GMT 2025 , Edited by admin on Mon Mar 31 22:42:16 GMT 2025
PRIMARY
CAS
34371-47-6
Created by admin on Mon Mar 31 22:42:16 GMT 2025 , Edited by admin on Mon Mar 31 22:42:16 GMT 2025
PRIMARY
Related Record Type Details
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