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(E)-3-[(2R)-1-methylpyrrolidin-2-yl]-N-[4-[3-methyl-4-([1,2,4]triazolo[4,3-c]pyrimidin-7-yloxy)anilino]quinazolin-6-yl]prop-2-enamide ID: ALA5179954
PubChem CID: 137376670
Max Phase: Preclinical
Molecular Formula: C28H27N9O2
Molecular Weight: 521.59
Associated Items:
Names and Identifiers Canonical SMILES: Cc1cc(Nc2ncnc3ccc(NC(=O)/C=C/[C@H]4CCCN4C)cc23)ccc1Oc1cc2nncn2cn1
Standard InChI: InChI=1S/C28H27N9O2/c1-18-12-19(6-9-24(18)39-27-14-25-35-32-17-37(25)16-31-27)34-28-22-13-20(5-8-23(22)29-15-30-28)33-26(38)10-7-21-4-3-11-36(21)2/h5-10,12-17,21H,3-4,11H2,1-2H3,(H,33,38)(H,29,30,34)/b10-7+/t21-/m1/s1
Standard InChI Key: LYIUENVBACZSCL-TYOLEZHBSA-N
Molfile:
RDKit 2D
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1.4210 1.2424 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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3.5699 1.6542 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0
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-5.1124 -0.0028 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.0260 -0.8255 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-5.7817 -1.1620 0.0000 N 0 0 0 0 0 0 0 0 0 0 0 0
-5.9960 -1.9616 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
-4.3091 -1.2394 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0
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11 16 1 0
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19 18 1 0
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33 34 1 0
34 35 1 0
35 36 1 0
37 36 1 0
37 33 1 0
37 38 1 0
36 39 1 6
28 39 2 0
M END Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 521.59Molecular Weight (Monoisotopic): 521.2288AlogP: 4.50#Rotatable Bonds: 7Polar Surface Area: 122.46Molecular Species: BASEHBA: 10HBD: 2#RO5 Violations: 1HBA (Lipinski): 11HBD (Lipinski): 2#RO5 Violations (Lipinski): 2CX Acidic pKa: ┄CX Basic pKa: 8.74CX LogP: 2.97CX LogD: 1.61Aromatic Rings: 5Heavy Atoms: 39QED Weighted: 0.30Np Likeness Score: -1.15
References 1. Li D, Tu Y, Jin K, Duan L, Hong Y, Xu J, Chen N, Zhang Z, Zuo H, Gong W, Zhang J, Wang Q, Qian H, Wang X, Ke Y, Xia G.. (2022) Discovery of SPH5030, a Selective, Potent, and Irreversible Tyrosine Kinase Inhibitor for HER2-Amplified and HER2-Mutant Cancer Treatment., 65 (7.0): [PMID:35319895 ] [10.1021/acs.jmedchem.1c00710 ]