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ID: ALA2336940
Max Phase: Preclinical
Molecular Formula: C21H41NO
Molecular Weight: 323.57
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(C)CCC[C@@H](C)[C@H]1CC[C@@]2(C)[C@@H](O)[C@@H](N(C)C)CC[C@]12C
Standard InChI: InChI=1S/C21H41NO/c1-15(2)9-8-10-16(3)17-11-13-21(5)19(23)18(22(6)7)12-14-20(17,21)4/h15-19,23H,8-14H2,1-7H3/t16-,17-,18+,19+,20-,21+/m1/s1
Standard InChI Key: WVTWWSDDOKFHMU-OUCVULTDSA-N
Associated Targets(Human)
HL-60 67320 Activities
3-beta-hydroxysteroid-delta(8),delta(7)-isomerase 102 Activities
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Associated Targets(non-human)
Yarrowia lipolytica 267 Activities
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Saccharomyces cerevisiae 19171 Activities
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Nakaseomyces glabratus 9108 Activities
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Molecule Features
| 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 |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 323.57 | Molecular Weight (Monoisotopic): 323.3188 | AlogP: 4.96 | #Rotatable Bonds: 6 |
| Polar Surface Area: 23.47 | Molecular Species: BASE | HBA: 2 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: 9.71 | CX LogP: 5.31 | CX LogD: 3.03 |
| Aromatic Rings: 0 | Heavy Atoms: 23 | QED Weighted: 0.75 | Np Likeness Score: 1.82 |
References
| 1. König M, Müller C, Bracher F.. (2013) Stereoselective synthesis of a new class of potent and selective inhibitors of human Δ8,7-sterol isomerase., 21 (7): [PMID:23433667] [10.1016/j.bmc.2013.01.041] |
Source
Source(1):