COCHLIOQUINOL

ID: ALA2288175

Max Phase: Preclinical

Molecular Formula: C31H46O8

Molecular Weight: 546.70

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC[C@H](C)C(=O)[C@@H](C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@H]4O[C@@H](C(C)(C)O)CC[C@]4(C)[C@H]3[C@@H]2O)[C@]1(O)CC(C)=O

Standard InChI:  InChI=1S/C31H46O8/c1-9-16(2)24(34)18(4)19-14-20(33)23-25(35)26-29(7)12-10-21(28(5,6)36)38-22(29)11-13-30(26,8)39-27(23)31(19,37)15-17(3)32/h14,16,18,21-22,25-26,35-37H,9-13,15H2,1-8H3/t16-,18-,21+,22+,25+,26+,29-,30+,31-/m0/s1

Standard InChI Key:  ZCSZZICIPVOPHV-KBOMQJRSSA-N

Associated Targets(non-human)

NADH-ubiquinone oxidoreductase chain 1 124 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Oryza sativa 2923 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Lolium multiflorum 260 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 546.70Molecular Weight (Monoisotopic): 546.3193AlogP: 3.60#Rotatable Bonds: 7
Polar Surface Area: 130.36Molecular Species: NEUTRALHBA: 8HBD: 3
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.65CX Basic pKa: CX LogP: 2.53CX LogD: 2.53
Aromatic Rings: 0Heavy Atoms: 39QED Weighted: 0.44Np Likeness Score: 2.05

References

1. LIM C, MIYAGAWA H, AKAMATSU M, NAKAGAWA Y, UENO T.  (1998)  Structures and Biological Activities of Phytotoxins Produced by the Plant Pathogenic Fungus Bipolaris cynodontis cynA,  23  (3): [10.1584/jpestics.23.281]

Source