ID: ALA4531265

Max Phase: Preclinical

Molecular Formula: C41H59NO5

Molecular Weight: 645.93

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)O[C@H]1C[C@]2(C)[C@H]3CC=C4[C@@H]5CC(C)(C)CC[C@]5(C(=O)NCc5ccccc5)CC[C@@]4(C)[C@]3(C)CC[C@H]2C(C)(C)[C@@H]1OC(C)=O

Standard InChI:  InChI=1S/C41H59NO5/c1-26(43)46-31-24-38(7)32(37(5,6)34(31)47-27(2)44)17-18-40(9)33(38)16-15-29-30-23-36(3,4)19-21-41(30,22-20-39(29,40)8)35(45)42-25-28-13-11-10-12-14-28/h10-15,30-34H,16-25H2,1-9H3,(H,42,45)/t30-,31-,32-,33+,34+,38-,39+,40+,41-/m0/s1

Standard InChI Key:  BFRXPUWFFUXTML-FGGFFJFQSA-N

Associated Targets(Human)

518A2 464 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

FaDu 1726 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

HT-29 80576 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

A2780 11979 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SW-1736 356 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

NIH3T3 5395 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: 645.93Molecular Weight (Monoisotopic): 645.4393AlogP: 8.58#Rotatable Bonds: 5
Polar Surface Area: 81.70Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 2HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 0.40CX LogP: 7.54CX LogD: 7.54
Aromatic Rings: 1Heavy Atoms: 47QED Weighted: 0.26Np Likeness Score: 2.17

References

1. Sommerwerk S, Heller L, Kuhfs J, Csuk R..  (2016)  Urea derivates of ursolic, oleanolic and maslinic acid induce apoptosis and are selective cytotoxic for several human tumor cell lines.,  119  [PMID:27149037] [10.1016/j.ejmech.2016.04.051]

Source