ID: ALA4795561

Max Phase: Preclinical

Molecular Formula: C30H38O7

Molecular Weight: 510.63

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)c1ccc(C)cc1

Standard InChI:  InChI=1S/C30H38O7/c1-16-7-9-19(10-8-16)27(35)37-26-20-13-21(32)24-29(15-36-18(3)31)12-6-11-28(4,5)22(29)14-23(33)30(24,26)25(34)17(20)2/h7-10,20-24,26,32-33H,2,6,11-15H2,1,3-5H3/t20-,21+,22-,23-,24+,26-,29+,30-/m1/s1

Standard InChI Key:  ZYKCBKYYQKPKBE-MNKYEVJKSA-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: 510.63Molecular Weight (Monoisotopic): 510.2618AlogP: 3.78#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: 3.94CX LogD: 3.94
Aromatic Rings: 1Heavy Atoms: 37QED Weighted: 0.47Np Likeness Score: 2.51

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