(Q104398605)

English

trans-Dehydrocrotonin

chemical compound

In more languages

Statements

type of chemical entity

0 references

5'-(Furan-3-yl)-4,7-dimethylspiro[1,4a,5,6,7,8a-hexahydronaphthalene-8,3'-oxolane]-2,2'-dione

1 reference

based on heuristic

inferred from SMILES

Dehydrocrotonin

1 reference

based on heuristic

inferred from SMILES

(1R,2R,4aR,5'R)-5'-(furan-3-yl)-2,5-dimethyl-2,3,4,4a,8,8a-hexahydrospiro[naphthalene-1,3'-oxolane]-2',7-dione

1 reference

based on heuristic

inferred from SMILES

Dehydrocrotonin[terpene]

1 reference

based on heuristic

inferred from SMILES

314.151809184 dalton

1 reference

based on heuristic

inferred from SMILES

stereoisomer of

cis-Dehydrocrotonin

1 reference

based on heuristic

inferred from InChI

chemical formula

C₁₉H₂₂O₄

0 references

canonical SMILES

O=C1OC(C2=COC=C2)CC13C(C)CCC4C(=CC(=O)CC43)C

0 references

isomeric SMILES

CC1=CC(=O)C[C@H]2[C@H]1CC[C@@H](C)[C@]21C[C@H](c2ccoc2)OC1=O

0 references

Croton cajucara

9 references

Insect growth inhibitory nor-diterpenes, cis-dehydrocrotonin and trans-dehydrocrotonin, from Croton cajucara

Investigation of genotoxic activity of trans-dehydrocrotonin, a clerodane diterpene from Croton cajucara

Ethnopharmacology, phytochemistry and pharmacology: a successful combination in the study of Croton cajucara

Investigation of anti-inflammatory and antinociceptive activities of trans-dehydrocrotonin, a 19-nor-clerodane diterpene from Croton cajucara. Part 1

Antiulcerogenic activity of trans-dehydrocrotonin from Croton cajucara.

Hypoglycemic effect of trans-dehydrocrotonin, a nor-clerodane diterpene from Croton cajucara

Terpenoids from Croton cajucara

Cytotoxicity of derivatives from dehydrocrotonin on V79 cells and Escherichia coli

Investigation of anti-inflammatory and antinociceptive activities of trans-dehydrocrotonin, a 19-nor-clerodane diterpene from Croton cajucara. Part 1

Croton schiedeanus

3 references

Neo-clerodane diterpenoids from Croton schiedeanus

Neo-clerodane diterpenoids from Croton schiedeanus

Neo-clerodane diterpenoids from Croton schiedeanus

Croton glabellus

1 reference

Absolute configuration assignments by experimental and theoretical approaches of ent-labdane- and cis-ent-clerodane-type diterpenes isolated from Croton glabellus

Identifiers

InChI=1S/C19H22O4/c1-11-7-14(20)8-16-15(11)4-3-12(2)19(16)9-17(23-18(19)21)13-5-6-22-10-13/h5-7,10,12,15-17H,3-4,8-9H2,1-2H3/t12-,15+,16+,17-,19-/m1/s1

0 references

PHTWCRQCDPNVLQ-WCARXYILSA-N

0 references

CAS Registry Number

1 reference

CAS (formerly Chemical Abstracts Service)

25 January 2022

2 references

17 September 2022

based on heuristic

inferred from InChIKey

matched by identifier from

PHTWCRQCDPNVLQ-WCARXYILSA-N

UniChem compound ID

1 reference

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q104398605&oldid=2167568543"