(12S)-11alpha,14alpha-epoxy-13alpha,14beta,15-trihydroxycyath-3-ene

ID: ALA5290128

Chembl Id: CHEMBL5290128

Max Phase: Preclinical

Molecular Formula: C20H32O4

Molecular Weight: 336.47

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(C)C1=C2[C@H]3C[C@H]4O[C@](O)([C@H](O)[C@@H]4CO)[C@]3(C)CC[C@@]2(C)CC1

Standard InChI:  InChI=1S/C20H32O4/c1-11(2)12-5-6-18(3)7-8-19(4)14(16(12)18)9-15-13(10-21)17(22)20(19,23)24-15/h11,13-15,17,21-23H,5-10H2,1-4H3/t13-,14-,15-,17-,18-,19-,20-/m1/s1

Standard InChI Key:  IQCGVKTZKMKJLD-NRICFRBZSA-N

Alternative Forms

  1. Parent:

    ALA5290128

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Associated Targets(non-human)

BV-2 (3710 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PC-12 (7051 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: YesOral: 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

Calculated Properties

Molecular Weight: 336.47Molecular Weight (Monoisotopic): 336.2301AlogP: 2.62#Rotatable Bonds: 2
Polar Surface Area: 69.92Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 10.77CX Basic pKa: CX LogP: 2.35CX LogD: 2.35
Aromatic Rings: 0Heavy Atoms: 24QED Weighted: 0.68Np Likeness Score: 2.85

References

1. Tang D, Xu YZ, Wang WW, Yang Z, Liu B, Stadler M, Liu LL, Gao JM..  (2019)  Cyathane Diterpenes from Cultures of the Bird's Nest Fungus Cyathus hookeri and Their Neurotrophic and Anti-neuroinflammatory Activities.,  82  (6.0): [PMID:31244147] [10.1021/acs.jnatprod.9b00091]

Source