US9227969, 93

ID: ALA3971755

Chembl Id: CHEMBL3971755

PubChem CID: 117876710

Max Phase: Preclinical

Molecular Formula: C28H23ClF2N6O2

Molecular Weight: 548.98

Molecule Type: Small molecule

Associated Items:

Names and Identifiers

Canonical SMILES:  CC(=O)N1CC[C@H](n2c(C)nc3cnc4cc(F)c(-c5ccc(Oc6ncccn6)cc5Cl)cc4c32)[C@@H](F)C1

Standard InChI:  InChI=1S/C28H23ClF2N6O2/c1-15-35-25-13-34-24-12-22(30)19(18-5-4-17(10-21(18)29)39-28-32-7-3-8-33-28)11-20(24)27(25)37(15)26-6-9-36(16(2)38)14-23(26)31/h3-5,7-8,10-13,23,26H,6,9,14H2,1-2H3/t23-,26-/m0/s1

Standard InChI Key:  AZEYBYPICMMZFR-OZXSUGGESA-N

Associated Targets(Human)

RAF1 Tclin Serine/threonine-protein kinase RAF and Dual specificity mitogen-activated protein kinase kinase 1 (Raf/MEK) (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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

Calculated Properties

Molecular Weight: 548.98Molecular Weight (Monoisotopic): 548.1539AlogP: 6.07#Rotatable Bonds: 4
Polar Surface Area: 86.03Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 2HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 2
CX Acidic pKa: CX Basic pKa: 3.48CX LogP: 3.87CX LogD: 3.87
Aromatic Rings: 5Heavy Atoms: 39QED Weighted: 0.27Np Likeness Score: -1.31

References

1.  (2016)  Compounds and compositions as inhibitors of MEK, 
2. Poddutoori R, Aardalen K, Aithal K, Barahagar SS, Belliappa C, Bock M, Chelur S, Gerken A, Gopinath S, Gruenenfelder B, Kiffe M, Krishnaswami M, Langowski J, Madapa S, Narayanan K, Pandit C, Panigrahi SK, Perrone M, Potakamuri RK, Ramachandra M, Ramanathan A, Ramos R, Sager E, Samajdar S, Subramanya HS, Thimmasandra DS, Venetsanakos E, Möbitz H..  (2022)  Discovery of MAP855, an Efficacious and Selective MEK1/2 Inhibitor with an ATP-Competitive Mode of Action.,  65  (5.0): [PMID:35195996] [10.1021/acs.jmedchem.1c02192]