Cassaidine
AlkaPlorer ID: AK042653
Synonym: '', 'Cassaidine'
IUPAC Name: 2-(dimethylamino)ethyl (2E)-2-[(1R,4aR,4bR,7S,8aR,10S,10aS)-7,10-dihydroxy-1,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene]acetate
Structure
SMILES: C[C@H]1/C(=C/C(=O)OCCN(C)C)CC[C@@H]2[C@H]1[C@@H](O)C[C@H]1C(C)(C)[C@@H](O)CC[C@]21C
InChI: InChI=1S/C24H41NO4/c1-15-16(13-21(28)29-12-11-25(5)6)7-8-17-22(15)18(26)14-19-23(2,3)20(27)9-10-24(17,19)4/h13,15,17-20,22,26-27H,7-12,14H2,1-6H3/b16-13+/t15-,17+,18-,19-,20-,22-,24+/m0/s1
InChIKey: JKPVSFQJGXEMSU-PRFGHTJTSA-N
Reference
Tumour inhibitory plants. New alkaloids from the bark of Erythrophleum chlorostachys (Leguminosae)
PubChem CID: 162959778
LOTUS: LTS0093194
SuperNatural Ⅲ: SN0167991-03
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Erythrophleum chlorostachys | Erythrophleum | Fabaceae | Fabales | Magnoliopsida | Streptophyta | Viridiplantae | Eukaryota |
Properties Information
Molecule Weight: 407.59500000000025
TPSA？: 70.0
MolLogP？: 3.2479000000000022
Number of H-Donors: 2
Number of H-Acceptors: 5
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|