ID: ALA4435129

Max Phase: Preclinical

Molecular Formula: C25H36O3

Molecular Weight: 384.56

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC1=CC(=O)[C@H]2/C(C)=C\C[C@@H]3[C@](C)(CC[C@@]34O[C@@H](/C=C(\C)CO)C[C@@H]4C)C[C@H]12

Standard InChI:  InChI=1S/C25H36O3/c1-15(14-26)10-19-12-18(4)25(28-19)9-8-24(5)13-20-17(3)11-21(27)23(20)16(2)6-7-22(24)25/h6,10-11,18-20,22-23,26H,7-9,12-14H2,1-5H3/b15-10+,16-6-/t18-,19-,20+,22+,23-,24+,25-/m0/s1

Standard InChI Key:  PHQVUIFBPMYMSK-ANFFYHJZSA-N

Associated Targets(Human)

SW1990 722 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MDA-MB-231 73002 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HepG2 196354 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

RAW264.7 28094 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

Properties

Molecular Weight: 384.56Molecular Weight (Monoisotopic): 384.2664AlogP: 5.01#Rotatable Bonds: 2
Polar Surface Area: 46.53Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.33CX LogD: 4.33
Aromatic Rings: 0Heavy Atoms: 28QED Weighted: 0.68Np Likeness Score: 3.40

References

1. Liu M, Sun W, Shen L, Hao X, Al Anbari WH, Lin S, Li H, Gao W, Wang J, Hu Z, Zhang Y..  (2019)  Bipolaricins A-I, Ophiobolin-Type Tetracyclic Sesterterpenes from a Phytopathogenic Bipolaris sp. Fungus.,  82  (10): [PMID:31573805] [10.1021/acs.jnatprod.9b00744]

Source