ID: ALA4878607

Max Phase: Preclinical

Molecular Formula: C26H38F6O4

Molecular Weight: 528.57

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  C[C@]12CC[C@H]3[C@@H](CC=C4C[C@@H](OCCO)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/C26H38F6O4/c1-22-9-7-16(36-12-11-33)13-15(22)3-4-17-18-5-6-20(23(18,2)10-8-19(17)22)21(34)14-24(35,25(27,28)29)26(30,31)32/h3,16-21,33-35H,4-14H2,1-2H3/t16-,17-,18-,19-,20+,21+,22-,23-/m0/s1

Standard InChI Key:  JJYZJTJEAOPZOA-JIJMJNLVSA-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: 528.57Molecular Weight (Monoisotopic): 528.2674AlogP: 5.55#Rotatable Bonds: 6
Polar Surface Area: 69.92Molecular Species: NEUTRALHBA: 4HBD: 3
#RO5 Violations: 2HBA (Lipinski): 4HBD (Lipinski): 3#RO5 Violations (Lipinski): 2
CX Acidic pKa: 7.91CX Basic pKa: CX LogP: 4.23CX LogD: 4.12
Aromatic Rings: 0Heavy Atoms: 36QED Weighted: 0.31Np Likeness Score: 1.68

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