ID: ALA4634244

Max Phase: Preclinical

Molecular Formula: C10H14O3

Molecular Weight: 182.22

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC1(C)CC(O)CC2=C1C(=O)OC2

Standard InChI:  InChI=1S/C10H14O3/c1-10(2)4-7(11)3-6-5-13-9(12)8(6)10/h7,11H,3-5H2,1-2H3

Standard InChI Key:  VCYAGNPYGLPDKO-UHFFFAOYSA-N

Associated Targets(non-human)

NRK-52E 51 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 182.22Molecular Weight (Monoisotopic): 182.0943AlogP: 1.02#Rotatable Bonds: 0
Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.13CX Basic pKa: CX LogP: 0.80CX LogD: 0.80
Aromatic Rings: 0Heavy Atoms: 13QED Weighted: 0.57Np Likeness Score: 2.57

References

1. Cao YG, Zhang YL, Zeng MN, Qi M, Ren YJ, Liu YL, Zhao X, Zheng XK, Feng WS..  (2020)  Renoprotective Mono- and Triterpenoids from the Fruit of Gardenia jasminoides.,  83  (4): [PMID:32141747] [10.1021/acs.jnatprod.9b01119]

Source