ID: ALA3904515

Max Phase: Preclinical

Molecular Formula: C20H34O3

Molecular Weight: 322.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C/C1=C\CC[C@]2(C)O[C@@H]2C[C@]2(C(C)C)CC[C@@](C)(O2)[C@@H](O)CC1

Standard InChI:  InChI=1S/C20H34O3/c1-14(2)20-12-11-18(4,23-20)16(21)9-8-15(3)7-6-10-19(5)17(13-20)22-19/h7,14,16-17,21H,6,8-13H2,1-5H3/b15-7+/t16-,17+,18+,19-,20-/m0/s1

Standard InChI Key:  ARTVDMKLQDTMGX-JOHZDJNTSA-N

Associated Targets(Human)

Signal transducer and activator of transcription 3 3313 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Heat sensitive channel TRPV3 59 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: 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: 322.49Molecular Weight (Monoisotopic): 322.2508AlogP: 4.38#Rotatable Bonds: 1
Polar Surface Area: 41.99Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.99CX Basic pKa: CX LogP: 3.78CX LogD: 3.78
Aromatic Rings: 0Heavy Atoms: 23QED Weighted: 0.58Np Likeness Score: 3.23

References

1. Pollastro F, Golin S, Chianese G, Putra MY, Schiano Moriello A, De Petrocellis L, García V, Munoz E, Taglialatela-Scafati O, Appendino G..  (2016)  Neuroactive and Anti-inflammatory Frankincense Cembranes: A Structure-Activity Study.,  79  (7): [PMID:27352042] [10.1021/acs.jnatprod.6b00141]

Source