ID: ALA4580421

Max Phase: Preclinical

Molecular Formula: C28H40F3NO9

Molecular Weight: 477.60

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C1C(=O)[C@]23[C@H](OC(=O)[C@H](C)N)[C@H]1C[C@H](O)[C@H]2[C@]1(COC(C)=O)CCCC(C)(C)[C@H]1C[C@H]3OC.O=C(O)C(F)(F)F

Standard InChI:  InChI=1S/C26H39NO7.C2HF3O2/c1-13-16-10-17(29)20-25(12-33-15(3)28)9-7-8-24(4,5)18(25)11-19(32-6)26(20,21(13)30)22(16)34-23(31)14(2)27;3-2(4,5)1(6)7/h14,16-20,22,29H,1,7-12,27H2,2-6H3;(H,6,7)/t14-,16-,17-,18+,19+,20-,22+,25-,26+;/m0./s1

Standard InChI Key:  UWJVJFGEAHLYRO-HBVLXACBSA-N

Associated Targets(Human)

TE-1 337 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MCF7 126967 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

A549 127892 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

MGC-803 6426 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: 477.60Molecular Weight (Monoisotopic): 477.2727AlogP: 2.16#Rotatable Bonds: 5
Polar Surface Area: 125.15Molecular Species: NEUTRALHBA: 8HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.14CX LogP: 1.66CX LogD: 1.47
Aromatic Rings: 0Heavy Atoms: 34QED Weighted: 0.46Np Likeness Score: 2.94

References

1. Ke Y, Hu TX, Huo JF, Yan JK, Wang JY, Yang RH, Xie H, Liu Y, Wang N, Zheng ZJ, Sun YX, Wang C, Du J, Liu HM..  (2019)  Synthesis and in vitro biological evaluation of novel derivatives of Flexicaulin A condensation with amino acid trifluoroacetate.,  182  [PMID:31494472] [10.1016/j.ejmech.2019.111645]

Source