ID: ALA4643017

Max Phase: Preclinical

Molecular Formula: C10H16O2

Molecular Weight: 168.24

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC1=CC(=O)CC(C)(C)[C@@H]1CO

Standard InChI:  InChI=1S/C10H16O2/c1-7-4-8(12)5-10(2,3)9(7)6-11/h4,9,11H,5-6H2,1-3H3/t9-/m1/s1

Standard InChI Key:  KURIDZCRFQNRTO-SECBINFHSA-N

Associated Targets(non-human)

NRK-52E 51 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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: 168.24Molecular Weight (Monoisotopic): 168.1150AlogP: 1.54#Rotatable Bonds: 1
Polar Surface Area: 37.30Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 1.24CX LogD: 1.24
Aromatic Rings: 0Heavy Atoms: 12QED Weighted: 0.64Np Likeness Score: 2.68

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