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ID: ALA1627337
Max Phase: Preclinical
Molecular Formula: C18H23FO2
Molecular Weight: 290.38
Molecule Type: Small molecule
Associated Items:
ID: ALA1627337
Max Phase: Preclinical
Molecular Formula: C18H23FO2
Molecular Weight: 290.38
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C[C@]12CC[C@@H]3c4ccc(O)c(F)c4CC[C@H]3[C@@H]1CC[C@@H]2O
Standard InChI: InChI=1S/C18H23FO2/c1-18-9-8-11-10-4-6-15(20)17(19)13(10)3-2-12(11)14(18)5-7-16(18)21/h4,6,11-12,14,16,20-21H,2-3,5,7-9H2,1H3/t11-,12-,14+,16+,18+/m1/s1
Standard InChI Key: QZFXMXJXAUMHQR-ZHIYBZGJSA-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: 290.38 | Molecular Weight (Monoisotopic): 290.1682 | AlogP: 3.75 | #Rotatable Bonds: 0 |
Polar Surface Area: 40.46 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 8.83 | CX Basic pKa: | CX LogP: 3.89 | CX LogD: 3.87 |
Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.76 | Np Likeness Score: 1.71 |
1. Heiman DF, Senderoff SG, Katzenellenbogen JA, Neeley RJ.. (1980) Estrogen receptor based imaging agents. 1. Synthesis and receptor binding affinity of some aromatic and D-ring halogenated estrogens., 23 (9): [PMID:7411555] [10.1021/jm00183a007] |
2. Poirier D, Roy J, Cortés-Benítez F, Dutour R.. (2016) Targeting cytochrome P450 (CYP) 1B1 with steroid derivatives., 26 (21): [PMID:27687674] [10.1016/j.bmcl.2016.09.046] |
3. Adhikari N, Baidya SK, Jha T.. (2020) Effective anti-aromatase therapy to battle against estrogen-mediated breast cancer: Comparative SAR/QSAR assessment on steroidal aromatase inhibitors., 208 [PMID:33017749] [10.1016/j.ejmech.2020.112845] |
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