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ID: ALA1271000
Max Phase: Preclinical
Molecular Formula: C30H43N5O3S
Molecular Weight: 553.77
Molecule Type: Small molecule
Associated Items:
ID: ALA1271000
Max Phase: Preclinical
Molecular Formula: C30H43N5O3S
Molecular Weight: 553.77
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ncnc(C)c1C(=O)N1C[C@H]2CN(CCC(c3ccccc3)C3CCN(S(=O)(=O)C(C)C)CC3)C[C@H]2C1
Standard InChI: InChI=1S/C30H43N5O3S/c1-21(2)39(37,38)35-14-10-25(11-15-35)28(24-8-6-5-7-9-24)12-13-33-16-26-18-34(19-27(26)17-33)30(36)29-22(3)31-20-32-23(29)4/h5-9,20-21,25-28H,10-19H2,1-4H3/t26-,27+,28?
Standard InChI Key: YWUQJCUUNVCNFS-FITHBNAOSA-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: 553.77 | Molecular Weight (Monoisotopic): 553.3087 | AlogP: 3.72 | #Rotatable Bonds: 8 |
Polar Surface Area: 86.71 | Molecular Species: BASE | HBA: 6 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 9.86 | CX LogP: 1.70 | CX LogD: -0.72 |
Aromatic Rings: 2 | Heavy Atoms: 39 | QED Weighted: 0.50 | Np Likeness Score: -0.90 |
1. Wanner J, Chen L, Lemoine RC, Kondru R, Jekle A, Heilek G, deRosier A, Ji C, Berry PW, Rotstein DM.. (2010) Evaluation of amide replacements in CCR5 antagonists as a means to increase intrinsic permeability. Part 2: SAR optimization and pharmacokinetic profile of a homologous azacyle series., 20 (22): [PMID:20855212] [10.1016/j.bmcl.2010.08.118] |
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