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ID: ALA4095072
Max Phase: Preclinical
Molecular Formula: C24H27N7O
Molecular Weight: 429.53
Molecule Type: Small molecule
Associated Items:
ID: ALA4095072
Max Phase: Preclinical
Molecular Formula: C24H27N7O
Molecular Weight: 429.53
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1n[nH]c(C)c1-c1ccc2c(NC(=O)c3ccc(N4CCN(C)CC4)cc3)n[nH]c2c1
Standard InChI: InChI=1S/C24H27N7O/c1-15-22(16(2)27-26-15)18-6-9-20-21(14-18)28-29-23(20)25-24(32)17-4-7-19(8-5-17)31-12-10-30(3)11-13-31/h4-9,14H,10-13H2,1-3H3,(H,26,27)(H2,25,28,29,32)
Standard InChI Key: SHJYUDRICHEQHX-UHFFFAOYSA-N
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Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
Chirality: No | Availability: No | Prodrug: No |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 429.53 | Molecular Weight (Monoisotopic): 429.2277 | AlogP: 3.57 | #Rotatable Bonds: 4 |
Polar Surface Area: 92.94 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 11.98 | CX Basic pKa: 7.74 | CX LogP: 3.22 | CX LogD: 2.72 |
Aromatic Rings: 4 | Heavy Atoms: 32 | QED Weighted: 0.46 | Np Likeness Score: -1.44 |
1. Fukuda T, Goto R, Kiho T, Ueda K, Muramatsu S, Hashimoto M, Aki A, Watanabe K, Tanaka N.. (2017) Discovery of DS79182026: A potent orally active hepcidin production inhibitor., 27 (16): [PMID:28705644] [10.1016/j.bmcl.2017.07.004] |
2. Fukuda T, Goto R, Kiho T, Ueda K, Muramatsu S, Hashimoto M, Aki A, Watanabe K, Tanaka N.. (2017) Discovery of DS28120313 as a potent orally active hepcidin production inhibitor: Design and optimization of novel 4,6-disubstituted indazole derivatives., 27 (23): [PMID:29079471] [10.1016/j.bmcl.2017.10.031] |
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