Impericine
AlkaPlorer ID: AK015692
Synonym: ''
IUPAC Name: (1R,2S,6S,9S,10R,11S,12S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-7-ene-12,17,20-triol
Structure
SMILES: C[C@@H]1[C@@H]2[C@@H](CN3C[C@@H](C)C=C[C@@H]13)[C@@H]1C[C@H]3[C@@H](C[C@@H](O)[C@H]4C[C@@H](O)CC[C@@]43C)[C@@H]1C[C@@H]2O
InChI: InChI=1S/C27H43NO3/c1-14-4-5-23-15(2)26-20(13-28(23)12-14)17-9-21-19(18(17)10-25(26)31)11-24(30)22-8-16(29)6-7-27(21,22)3/h4-5,14-26,29-31H,6-13H2,1-3H3/t14-,15-,16-,17+,18+,19-,20-,21-,22+,23-,24+,25-,26+,27+/m0/s1
InChIKey: BSHYJFKVJJHKEM-YHIXLZKYSA-N
Reference
New Steroidal Alkaloids from Fritillaria imperialis and Their Cholinesterase Inhibiting Activities.
PubChem CID: 10320454
LOTUS: LTS0151712
SuperNatural Ⅲ: SN0034111-04
NPASS: NPC255874
Source
Properties Information
Molecule Weight: 429.64500000000027
TPSA?: 63.93000000000001
MolLogP?: 3.3100000000000027
Number of H-Donors: 3
Number of H-Acceptors: 4
RingCount: 6
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
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