ID: ALA4861297

Max Phase: Preclinical

Molecular Formula: C24H32F6O3

Molecular Weight: 482.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@]12CC[C@H]3[C@@H](CC=C4CC(=O)CC[C@@]43C)[C@@H]1CC[C@@H]2[C@@H](O)CC(O)(C(F)(F)F)C(F)(F)F

Standard InChI:  InChI=1S/C24H32F6O3/c1-20-9-7-14(31)11-13(20)3-4-15-16-5-6-18(21(16,2)10-8-17(15)20)19(32)12-22(33,23(25,26)27)24(28,29)30/h3,15-19,32-33H,4-12H2,1-2H3/t15-,16-,17-,18+,19-,20-,21-/m0/s1

Standard InChI Key:  GCSMPSZKOFPDBF-UJPCIWJBSA-N

Associated Targets(Human)

KMS-11 183 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: 482.51Molecular Weight (Monoisotopic): 482.2256AlogP: 5.74#Rotatable Bonds: 3
Polar Surface Area: 57.53Molecular Species: NEUTRALHBA: 3HBD: 2
#RO5 Violations: 1HBA (Lipinski): 3HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 7.91CX Basic pKa: CX LogP: 4.49CX LogD: 4.37
Aromatic Rings: 0Heavy Atoms: 33QED Weighted: 0.40Np Likeness Score: 1.78

References

1. Castelli R, Taranto S, Furiassi L, Bozza N, Marseglia G, Ferlenghi F, Rivara S, Retini M, Bedini A, Spadoni G, Matarazzo S, Ronca R, Presta M, Mor M, Giacomini A..  (2021)  Chemical modification of NSC12 leads to a specific FGF-trap with antitumor activity in multiple myeloma.,  221  [PMID:34004471] [10.1016/j.ejmech.2021.113529]

Source