(Q27134675)

English

salaspermic acid

chemical compound

(3beta,20alpha)-3,24-epoxy-3-hydroxy-D:A-friedooleanan-29-oic acid

In more languages

Statements

type of chemical entity

0 references

1 reference

based on heuristic

inferred from SMILES

472.355±0 dalton

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

stereoisomer of

(1S,4S,5R,8R,11R,13R,14S,17R,18S,21S,24R)-21-hydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-11-carboxylic acid

1 reference

based on heuristic

inferred from InChI

(1R,4S,5R,8S,11R,13R,14S,17R,18S,21R,24R)-21-hydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.01,18.04,17.05,14.08,13]tetracosane-11-carboxylic acid

1 reference

based on heuristic

inferred from InChI

chemical formula

C₃₀H₄₈O₄

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

canonical SMILES

CC1C23CCC4C(C2CCC1(OC3)O)(CCC5(C4(CCC6(C5CC(CC6)(C)C(=O)O)C)C)C)C

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

isomeric SMILES

C[C@@H]1[C@@]23CC[C@H]4[C@]([C@@H]2CC[C@@]1(OC3)O)(CC[C@@]5([C@@]4(CC[C@@]6([C@H]5C[C@](CC6)(C)C(=O)O)C)C)C)C

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

Glyptopetalum sclerocarpum

1 reference

Constituents of the pericarp of Glyptopetalum sclerocarpum

Kokoona ochracea

1 reference

Quinone-methide triterpenes and salaspermic acid from Kokoona ochracea

Orthosphenia mexicana

1 reference

3-Oxo-28,29-Dihydroxyolean-12-Ene from Orthosphenia mexicana

Plenckia populnea

2 references

Epikatonic acid fromAustroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography

Epikatonic acid fromAustroplenckia populnea: structure elucidation by 2D NMR spectroscopy and X-ray crystallography

Salacia chinensis

4 references

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of new friedelane- and norfriedelane-type triterpenes and polyacylated eudesmane-type sesquiterpene from Salacia chinensis LINN. (S. prinoides DC., Hippocrateaceae) and radical scavenging activities of principal constituents

Structures of new friedelane-type triterpenes and eudesmane-type sesquiterpene and aldose reductase inhibitors from Salacia chinensis

Structures of New Friedelane- and Norfriedelane-Type Triterpenes and Polyacylated Eudesmane-Type Sesquiterpene from Salacia chinensis Linn. (S. prinoides DC., Hippocrateaceae) and Radical Scavenging Activities of Principal Constituents.

Tripterygium hypoglaucum

2 references

Di- and triterpenoids from Tripterygium hypoglaucum

Di- and triterpenoids from Tripterygium hypoglaucum

Tripterygium regelii

1 reference

Triterpenoids from Tripterygium wilfordii

Salacia macrosperma

2 references

Revised structures of the triterpenes Q, T, and U from Salacia prinoides DC; X-ray crystal structure of triterpene T

Salaspermic acid, a new triterpene acid from Salacia macrosperma Wight

Maytenus umbellata

1 reference

Taxonomy and chemotaxonomy of some species of celastraceae

Tripterygium wilfordii

6 references

Triterpenoids from Tripterygium wilfordii

Di- and triterpenoids from Tripterygium hypoglaucum

CHEMICAL CONSTITUENTS

Anti-aids agents, 6. Salaspermic acid, an anti-HIV principle from Tripterygium wilfordii, and the structure-activity correlation with its related compounds

Triterpenoid inhibitors of interleukin-1 secretion and tumour-promotion from Tripterygium wilfordii var. regelii

A novel epoxy-triterpene and nortriterpene from callus cultures of Tripterygium wilfordii

Monteverdia truncata

2 references

Triterpenes from Maytenus horrida

Antitumor Substtance from Higher Plants

Monteverdia ilicifolia

2 references

Triterpenes from Maytenus horrida

Antitumor Substtance from Higher Plants

Monteverdia laevis

1 reference

Chemical constituents from the colombian medicinal plant Niphogeton ternata

Identifiers

InChI=1S/C30H48O4/c1-19-29-9-7-20-26(4,21(29)8-10-30(19,33)34-18-29)14-16-28(6)22-17-25(3,23(31)32)12-11-24(22,2)13-15-27(20,28)5/h19-22,33H,7-18H2,1-6H3,(H,31,32)/t19-,20+,21+,22-,24-,25-,26-,27-,28+,29+,30+/m1/s1

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

ZXENWDWQTWYUGY-UUZWCOCASA-N

2 references

language of work or name

Salaspermic acid (English)

7 October 2016

ChEBI release 2020-09-01

CAS Registry Number

2 references

language of work or name

salaspermic acid (English)

7 October 2016

ZXENWDWQTWYUGY-UUZWCOCASA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=71247-78-4

1 reference

language of work or name

(1R,4S,5R,8S,11R,13R,14S,17R,18S,21S,24R)-21-Hydroxy-5,8,11,14,17,24-hexamethyl-22-oxahexacyclo[19.2.1.0~1,18~.0~4,17~.0~5,14~.0~8,13~]tetracosane-11-carboxylic acid (English)

7 October 2016

1 reference

language of work or name

Salaspermic acid (English)

7 October 2016

Reaxys registry number

4889115

1 reference

language of work or name

salaspermic acid (English)

7 October 2016

mapping relation type

1 reference

language of work or name

salaspermic acid (English)

7 October 2016

UniChem compound ID

1 reference

DSSTox substance ID

0 references

DSSTOX compound identifier

DTXCID801418638

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

30 June 2018

Sitelinks

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Multilingual sites(0 entries)

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