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ID: ALA12504
Max Phase: Preclinical
Molecular Formula: C12H17Cl3N2O2
Molecular Weight: 292.19
Molecule Type: Small molecule
Associated Items:
ID: ALA12504
Max Phase: Preclinical
Molecular Formula: C12H17Cl3N2O2
Molecular Weight: 292.19
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C[N+](CCCl)(CCCl)Cc1ccccc1[N+](=O)[O-].[Cl-]
Standard InChI: InChI=1S/C12H17Cl2N2O2.ClH/c1-16(8-6-13,9-7-14)10-11-4-2-3-5-12(11)15(17)18;/h2-5H,6-10H2,1H3;1H/q+1;/p-1
Standard InChI Key: XIEWWPGSKHFRTG-UHFFFAOYSA-M
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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: 292.19 | Molecular Weight (Monoisotopic): 291.0662 | AlogP: 3.02 | #Rotatable Bonds: 7 |
Polar Surface Area: 43.14 | Molecular Species: | HBA: 2 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: | CX LogD: |
Aromatic Rings: 1 | Heavy Atoms: 18 | QED Weighted: 0.34 | Np Likeness Score: -0.61 |
1. Tercel M, Wilson WR, Anderson RF, Denny WA.. (1996) Hypoxia-selective antitumor agents. 12. Nitrobenzyl quaternary salts as bioreductive prodrugs of the alkylating agent mechlorethamine., 39 (5): [PMID:8676343] [10.1021/jm9507791] |
2. Tercel M, Wilson WR, Denny WA.. (1993) Nitrobenzyl mustard quaternary salts: a new class of hypoxia-selective cytotoxins showing very high in vitro selectivity., 36 (17): [PMID:8355257] [10.1021/jm00069a019] |
3. Tercel M, Lee AE, Hogg A, Anderson RF, Lee HH, Siim BG, Denny WA, Wilson WR.. (2001) Hypoxia-selective antitumor agents. 16. Nitroarylmethyl quaternary salts as bioreductive prodrugs of the alkylating agent mechlorethamine., 44 (21): [PMID:11585455] [10.1021/jm010202l] |
Source(1):