| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3342898
Max Phase: Preclinical
Molecular Formula: C28H36N2O3
Molecular Weight: 448.61
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@]12CC[C@H](OC(=O)C3CCC3)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(n3ccnc3)=C(C=O)C[C@@H]12
Standard InChI: InChI=1S/C28H36N2O3/c1-27-10-8-21(33-26(32)18-4-3-5-18)15-20(27)6-7-22-23(27)9-11-28(2)24(22)14-19(16-31)25(28)30-13-12-29-17-30/h6,12-13,16-18,21-24H,3-5,7-11,14-15H2,1-2H3/t21-,22+,23-,24-,27-,28-/m0/s1
Standard InChI Key: ZRTXIAQHQGBTMK-UAGBHOFDSA-N
Associated Targets(Human)
Steroid 5-alpha-reductase 2 937 Activities
Associated Targets(non-human)
Steroid 5-alpha-reductase 1 193 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Androgen Receptor 5522 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 448.61 | Molecular Weight (Monoisotopic): 448.2726 | AlogP: 5.58 | #Rotatable Bonds: 4 |
| Polar Surface Area: 61.19 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
| #RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: | CX Basic pKa: 6.10 | CX LogP: 4.00 | CX LogD: 3.99 |
| Aromatic Rings: 1 | Heavy Atoms: 33 | QED Weighted: 0.34 | Np Likeness Score: 0.83 |
References
| 1. Bratoeff E, Garrido M, Ramírez-Apan T, Heuze Y, Sánchez A, Soriano J, Cabeza M.. (2014) Effect of dehydroepiandrosterone derivatives on the activity of 5α-reductase isoenzymes and on cancer cell line PC-3., 22 (21): [PMID:25261928] [10.1016/j.bmc.2014.08.019] |
Source
Source(1):