ID: ALA2387206

Max Phase: Preclinical

Molecular Formula: C24H30O8

Molecular Weight: 446.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C=C(C)[C@@]12OC3(C)O[C@@H]1[C@@H]1C=C(CO)C[C@]4(O)C(=O)C(C)=C[C@H]4[C@@]1(O3)[C@H](C)[C@H]2OC(C)=O

Standard InChI:  InChI=1S/C24H30O8/c1-11(2)23-19(29-14(5)26)13(4)24-16(20(23)30-21(6,31-23)32-24)8-15(10-25)9-22(28)17(24)7-12(3)18(22)27/h7-8,13,16-17,19-20,25,28H,1,9-10H2,2-6H3/t13-,16+,17-,19-,20-,21?,22-,23+,24-/m1/s1

Standard InChI Key:  PXFYLWZOFVKKBG-AOXXXCAZSA-N

Associated Targets(non-human)

B16 5829 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: 446.50Molecular Weight (Monoisotopic): 446.1941AlogP: 1.56#Rotatable Bonds: 3
Polar Surface Area: 111.52Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 12.59CX Basic pKa: CX LogP: 1.52CX LogD: 1.52
Aromatic Rings: 0Heavy Atoms: 32QED Weighted: 0.50Np Likeness Score: 3.51

References

1. Bang KK, Yun CY, Lee C, Jin Q, Lee JW, Jung SH, Lee D, Lee MK, Hong JT, Kim Y, Hwang BY..  (2013)  Melanogenesis inhibitory daphnane diterpenoids from the flower buds of Daphne genkwa.,  23  (11): [PMID:23623417] [10.1016/j.bmcl.2013.03.096]

Source