ID: ALA4796996

Max Phase: Preclinical

Molecular Formula: C30H35F3O7

Molecular Weight: 564.60

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C1C(=O)[C@@]23[C@H](O)C[C@@H]4C(C)(C)CCC[C@@]4(COC(C)=O)[C@@H]2[C@@H](O)C[C@H]1[C@H]3OC(=O)c1cccc(C(F)(F)F)c1

Standard InChI:  InChI=1S/C30H35F3O7/c1-15-19-12-20(35)23-28(14-39-16(2)34)10-6-9-27(3,4)21(28)13-22(36)29(23,24(15)37)25(19)40-26(38)17-7-5-8-18(11-17)30(31,32)33/h5,7-8,11,19-23,25,35-36H,1,6,9-10,12-14H2,2-4H3/t19-,20+,21-,22-,23+,25-,28+,29-/m1/s1

Standard InChI Key:  ZTDXOFMKSCVSPJ-PGSPYRNJSA-N

Associated Targets(Human)

ECa-109 cell line 1254 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

TE-1 337 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MGC-803 6426 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 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: 564.60Molecular Weight (Monoisotopic): 564.2335AlogP: 4.49#Rotatable Bonds: 4
Polar Surface Area: 110.13Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: CX LogP: 4.30CX LogD: 4.30
Aromatic Rings: 1Heavy Atoms: 40QED Weighted: 0.41Np Likeness Score: 2.08

References

1. Huo JF,Hu TX,Dong YL,Zhao JZ,Liu XJ,Li LL,Zhang XY,Li YF,Liu HM,Ke Y,Wang C.  (2020)  Synthesis and in vitro and in vivo biological evaluation of novel derivatives of flexicaulin A as antiproliferative agents.,  208  [PMID:32883640] [10.1016/j.ejmech.2020.112789]

Source