Antiquorpene F

ID: ALA4535258

PubChem CID: 155547801

Max Phase: Preclinical

Molecular Formula: C24H34O5

Molecular Weight: 402.53

Molecule Type: Unknown

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  C=C1C[C@@]23CC[C@H]4[C@@](C)(CCC(=O)[C@@]4(C)COC(=O)CCC)[C@@H]2C[C@@H]1[C@@H](O)C3=O

Standard InChI:  InChI=1S/C24H34O5/c1-5-6-19(26)29-13-23(4)16-7-10-24-12-14(2)15(20(27)21(24)28)11-17(24)22(16,3)9-8-18(23)25/h15-17,20,27H,2,5-13H2,1,3-4H3/t15-,16-,17-,20+,22+,23-,24-/m0/s1

Standard InChI Key:  UKHCDTUBQLXKSX-DAAZMYMBSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4535258

    ---

Associated Targets(non-human)

BV-2 (3710 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

Calculated Properties

Molecular Weight: 402.53Molecular Weight (Monoisotopic): 402.2406AlogP: 3.63#Rotatable Bonds: 4
Polar Surface Area: 80.67Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 13.08CX Basic pKa: CX LogP: 3.79CX LogD: 3.79
Aromatic Rings: Heavy Atoms: 29QED Weighted: 0.57Np Likeness Score: 2.96

References

1. Liang Y, An L, Shi Z, Zhang X, Xie C, Tuerhong M, Song Z, Ohizumi Y, Lee D, Shuai L, Xu J, Guo Y..  (2019)  Bioactive Diterpenoids from the Stems of Euphorbia antiquorum.,  82  (6): [PMID:31180680] [10.1021/acs.jnatprod.9b00134]

Source