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ID: ALA1271310
Max Phase: Preclinical
Molecular Formula: C32H45N5O2
Molecular Weight: 531.75
Molecule Type: Small molecule
Associated Items:
ID: ALA1271310
Max Phase: Preclinical
Molecular Formula: C32H45N5O2
Molecular Weight: 531.75
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ncnc(C)c1C(=O)N1C[C@H]2CN(CCC(c3ccccc3)C3CCN(C(=O)CC(C)C)CC3)C[C@H]2C1
Standard InChI: InChI=1S/C32H45N5O2/c1-22(2)16-30(38)36-14-10-26(11-15-36)29(25-8-6-5-7-9-25)12-13-35-17-27-19-37(20-28(27)18-35)32(39)31-23(3)33-21-34-24(31)4/h5-9,21-22,26-29H,10-20H2,1-4H3/t27-,28+,29?
Standard InChI Key: RABIKHKBVSVPHT-ULJKERAFSA-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: 531.75 | Molecular Weight (Monoisotopic): 531.3573 | AlogP: 4.56 | #Rotatable Bonds: 8 |
Polar Surface Area: 69.64 | Molecular Species: BASE | HBA: 5 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 7 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 9.86 | CX LogP: 2.56 | CX LogD: 0.14 |
Aromatic Rings: 2 | Heavy Atoms: 39 | QED Weighted: 0.50 | Np Likeness Score: -0.80 |
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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