ChemicalBook--->CAS DataBase List--->54483-84-0

54483-84-0

54483-84-0 Structure

54483-84-0 Structure
IdentificationBack Directory
[Name]

3-dihydrocadambine
[CAS]

54483-84-0
[Synonyms]

3-dihydrocadambine
3α-dihydrocadambine
3alpha-dihydrocadambine
Pyrano[4'',3'':4',5']azepino[1',2':1,2]pyrido[3,4-b]indole-1-carboxylic acid, 4-(β-D-glucopyranosyloxy)-4,4a,5,6,8,9,14,14b,15,15a-decahydro-5-hydroxy-, methyl ester, (4S,4aS,5S,14bS,15aS)-
Pyrano[4'',3'':4',5']azepino[1',2':1,2]pyrido[3,4-b]indole-1-carboxylic acid, 4-(β-D-glucopyranosyloxy)-4,4a,5,6,8,9,14,14b,15,15a-decahydro-5-hydroxy-, methyl ester, (4S,4aS,5S,14bS,15aS)-
[Molecular Formula]

C27H34N2O10
[MOL File]

54483-84-0.mol
[Molecular Weight]

546.57
Chemical PropertiesBack Directory
[Boiling point ]

802.9±65.0 °C(Predicted)
[density ]

1.56±0.1 g/cm3(Predicted)
[pka]

12.80±0.70(Predicted)
Hazard InformationBack Directory
[Uses]

3α-Dihydrocadambine is a natural product isolated from the heartwoods of Anthocephalus cadamba.3α-Dihydrocadambine exhibits dose-dependent hypotensive and anti-hypertensive effects in anesthetized normotensive rats and in conscious spontaneously hypertensive rats[1][2].
[References]

[1] Takayama H, et al. Gluco-indole alkaloids from Nauclea cadamba in Thailand and transformation of 3 alpha-dihydrocadambine into the indolopyridine alkaloid, 16-carbomethoxynaufoline. Chem Pharm Bull (Tokyo). 2003;51(2):232-233. DOI:10.1248/cpb.51.232
[2] K Aisaka, et al. Hypotensive action of 3 alpha-dihydrocadambine, an indole alkaloid glycoside of Uncaria hooks. Planta Med. 1985 Oct;51(5):424-7. DOI:10.1055/s-2007-969538
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