Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, compd. with cyclohexanamine (1:1)
CAS 1566-15-0 MFCD01566150
化学结构图
SMILES: NC1CCCCC1.NP(=O)(O)N(CCCl)CCCl
化学属性
| Mol. Formula | C10H24Cl2N3O2P |
|---|---|
| Mol. Weight | 320 |
别名和识别编码
| Chemical Name | PHOSPHORAMIDEMUSTARD |
|---|---|
| Chemicalbook ID | CB11447771 |
| Chemical Name Translation | |
| PubChem Substance ID | 96355 |
| InChI | InChI=1S/C6H13N.C4H11Cl2N2O2P/c7-6-4-2-1-3-5-6;5-1-3-8(4-2-6)11(7,9)10/h6H,1-5,7H2;1-4H2,(H3,7,9,10) |
| MDL Number | |
| CAS Number | 1566-15-0 |
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相关文献及参考
- [2]. S Genka, et al. Brain and plasma pharmacokinetics and anticancer activities of cyclophosphamide and phosphoramide mustard in the rat. Cancer Chemother Pharmacol. 1990;27(1):1-7.
- [1]. Shanthi Ganesan, et al. Phosphoramide mustard exposure induces DNA adduct formation and the DNA damage repair response in rat ovarian granulosa cells. Toxicol Appl Pharmacol. 2015 Feb 1; 282(3): 252–258.
- [1]. Shanthi Ganesan, et al. Phosphoramide mustard exposure induces DNA adduct formation and the DNA damage repair response in rat ovarian granulosa cells. Toxicol Appl Pharmacol. 2015 Feb 1; 282(3): 252–258.
- [2]. S Genka, et al. Brain and plasma pharmacokinetics and anticancer activities of cyclophosphamide and phosphoramide mustard in the rat. Cancer Chemother Pharmacol. 1990;27(1):1-7.
