ID: ALA3959869

Max Phase: Preclinical

Molecular Formula: C27H38O3

Molecular Weight: 410.60

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  C/C1=C\C[C@]2(C(C)C)CC[C@@](C)(O2)[C@@H](OC(=O)c2ccccc2)CC/C(C)=C/CC1

Standard InChI:  InChI=1S/C27H38O3/c1-20(2)27-17-16-22(4)11-9-10-21(3)14-15-24(26(5,30-27)18-19-27)29-25(28)23-12-7-6-8-13-23/h6-8,10,12-13,16,20,24H,9,11,14-15,17-19H2,1-5H3/b21-10+,22-16+/t24-,26+,27+/m0/s1

Standard InChI Key:  AKGLTDYPASAOIS-XEYDJRIMSA-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: 410.60Molecular Weight (Monoisotopic): 410.2821AlogP: 7.03#Rotatable Bonds: 3
Polar Surface Area: 35.53Molecular Species: NEUTRALHBA: 3HBD: 0
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 7.24CX LogD: 7.24
Aromatic Rings: 1Heavy Atoms: 30QED Weighted: 0.40Np Likeness Score: 2.22

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