ID: ALA5277783

Max Phase: Preclinical

Molecular Formula: C23H30O8

Molecular Weight: 434.49

Associated Items:

Representations

Canonical SMILES:  COC(=O)C1=CCC[C@H]2[C@@]13CC[C@@H](C)[C@]21C[C@@H](C2=CC(=O)O[C@H]2OC)O[C@@H]1O[C@@H]3OC

Standard InChI:  InChI=1S/C23H30O8/c1-12-8-9-22-14(18(25)26-2)6-5-7-16(22)23(12)11-15(29-21(23)31-20(22)28-4)13-10-17(24)30-19(13)27-3/h6,10,12,15-16,19-21H,5,7-9,11H2,1-4H3/t12-,15+,16+,19-,20+,21-,22-,23-/m1/s1

Standard InChI Key:  WLSDJQFEAYCAHU-IBGZWSFNSA-N

Associated Targets(non-human)

3T3-L1 3664 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 434.49Molecular Weight (Monoisotopic): 434.1941AlogP: 2.47#Rotatable Bonds: 4
Polar Surface Area: 89.52Molecular Species: ACIDHBA: 8HBD: 0
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: 5.92CX Basic pKa: CX LogP: 3.33CX LogD: 1.85
Aromatic Rings: 0Heavy Atoms: 31QED Weighted: 0.62Np Likeness Score: 3.02

References

1. Jiang ZY, Liu CJ, Niu Q, Yan XY, Xiao D, Zhang HL, Huang CQ, Shi SL, Zuo AX, He HP..  (2023)  In Vitro Hypoglycemic Diterpenoids from the Roots of Croton yunnanensis.,  86  (1.0): [PMID:36635870] [10.1021/acs.jnatprod.2c00970]

Source