Chondocurine; (-)-form, O6-De-Me, O7,O12-di-Me
AlkaPlorer ID: AK292395
Synonym: Racemosidine C
IUPAC Name: 9,21,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.118,22.027,31.016,34]hexatriaconta-3(36),4,6(35),8(34),9,11,18(33),19,21,24,26,31-dodecaen-10-ol
Structure
SMILES: COC1=CC=C2C=C1OC1=C(OC)C=C3CCN(C)C(CC4=CC=C(C=C4)OC4=C5C(=CC(O)=C4OC)CCN(C)C5C2)C3=C1
InChI: InChI=1S/C37H40N2O6/c1-38-14-12-24-20-32(42-4)34-21-27(24)28(38)16-22-6-9-26(10-7-22)44-37-35-25(19-30(40)36(37)43-5)13-15-39(2)29(35)17-23-8-11-31(41-3)33(18-23)45-34/h6-11,18-21,28-29,40H,12-17H2,1-5H3
InChIKey: DQFIZQYILFTDPW-UHFFFAOYSA-N
Reference
Cytotoxic Bisbenzylisoquinoline Alkaloids from the Roots of <i>Cyclea racemosa</i>
PubChem CID: 56678073
LOTUS: LTS0221081
COCONUT: CNP0372969.1
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Cyclea racemosa | Cyclea | Menispermaceae | Ranunculales | Magnoliopsida | Streptophyta | Viridiplantae | Eukaryota |
Properties Information
Molecule Weight: 608.735
TPSA？: 72.86
MolLogP？: 6.859400000000008
Number of H-Donors: 1
Number of H-Acceptors: 8
RingCount: 8
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|