Molecule

Ancistrocladine

AlkaPlorer ID: AK003223

Synonym: '', 'GEN25_39.1', '(+)-Hamatine', 'Ancistrocladine', 'Hamatine', 'Isoancistrocladine', 'ConMedNP.334', 'ConMedNP.335', '(-)-Ancistrocladine', 'GEN25_40.1'

IUPAC Name: (1S,3S)-5-(4,5-dimethoxy-2-methylnaphthalen-1-yl)-8-methoxy-1,3-dimethyl-1,2,3,4-tetrahydroisoquinolin-6-ol

Structure

SMILES: COC1=CC(O)=C(C2=C(C)C=C(OC)C3=C(OC)C=CC=C23)C2=C1[C@H](C)N[C@@H](C)C2

InChI: InChI=1S/C25H29NO4/c1-13-10-20(29-5)25-16(8-7-9-19(25)28-4)22(13)24-17-11-14(2)26-15(3)23(17)21(30-6)12-18(24)27/h7-10,12,14-15,26-27H,11H2,1-6H3/t14-,15-/m0/s1

InChIKey: XUFOYASAFNKRRE-GJZGRUSLSA-N

Reference

Activity of extracts and naphthylisoquinoline alkaloids from Triphyophyllum peltatum, Ancistrocladus abbreviatus and A. Barteri against Plasmodium falciparum in vitro☆

PubChem CID: 161741

CAS: 32221-59-3

LOTUS: LTS0196288

SuperNatural Ⅲ: SN0440256-02

NPASS: NPC141268

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Ancistrocladus korupensis	Ancistrocladus	Ancistrocladaceae	Caryophyllales	Magnoliopsida	Streptophyta	Viridiplantae	Eukaryota

Properties Information

Molecule Weight: 407.5100000000001

TPSA？: 59.95

MolLogP？: 5.1418200000000045

Number of H-Donors: 2

Number of H-Acceptors: 5

RingCount: 4

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi