ID: ALA4476455

Max Phase: Preclinical

Molecular Formula: C29H29F2N5O5

Molecular Weight: 565.58

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C=C1C(=O)O[C@H]2[C@H]1CC/C(Cn1cc(Cn3cc(F)c(=O)n(Cc4ccc(F)cc4)c3=O)nn1)=C\CC[C@@]1(C)O[C@@H]21

Standard InChI:  InChI=1S/C29H29F2N5O5/c1-17-22-10-7-18(4-3-11-29(2)25(41-29)24(22)40-27(17)38)12-35-15-21(32-33-35)14-34-16-23(31)26(37)36(28(34)39)13-19-5-8-20(30)9-6-19/h4-6,8-9,15-16,22,24-25H,1,3,7,10-14H2,2H3/b18-4+/t22-,24-,25-,29+/m0/s1

Standard InChI Key:  UDGKPJAUWWXSJE-LUEFZTOZSA-N

Associated Targets(Human)

Bel7402/5-FU 373 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Bel-7402 4577 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: 565.58Molecular Weight (Monoisotopic): 565.2137AlogP: 2.73#Rotatable Bonds: 6
Polar Surface Area: 113.54Molecular Species: NEUTRALHBA: 10HBD: 0
#RO5 Violations: 1HBA (Lipinski): 10HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 0.14CX LogP: 3.82CX LogD: 3.82
Aromatic Rings: 3Heavy Atoms: 41QED Weighted: 0.20Np Likeness Score: 0.42

References

1. Ding Y, Li S, Ge W, Liu Z, Zhang X, Wang M, Chen T, Chen Y, Zhang Q..  (2019)  Design and synthesis of parthenolide and 5-fluorouracil conjugates as potential anticancer agents against drug resistant hepatocellular carcinoma.,  183  [PMID:31553932] [10.1016/j.ejmech.2019.111706]

Source