PHOSPHORAMIDEMUSTARD

PHOSPHORAMIDEMUSTARD

中文名称PHOSPHORAMIDEMUSTARD
中文同义词PHOSPHAMIDE MUSTARD CYCLOHEXAMINE SALT;磷酰胺氮芥环己盐;N,N-双(2-氯乙基)磷二酰胺酸环己胺盐;N,N-BIS(2-CHLOROETHYL)PHOSPHORODIAMIDIC ACID COMPOUND WITH CYCLOHEXANAMINE (1:1);磷酰胺芥子-[D8]环己铵盐/精确称量;磷酰胺氮芥环己胺盐;磷酰胺氮芥环己胺盐(标准品)
英文名称PHOSPHORAMIDEMUSTARD
英文同义词Ai3-51834;Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, compd. with cyclohexanamine(1:1) (9ci);Phosphorodiamidic acid, N,N-bis(2-chloroethyl)-, compound with cyclohexanamine (1:1);N,N-Bis(2-chloroethyl)phosphorodiaMidic Acid CyclohexylaMine Salt;amino-[bis(2-chloroethyl)amino]phosphinic acid,cyclohexanamine;Phosphamide Mustard;Phosphamide Mustard Cyclohexamine Salt;Phosphoramide mustard cyclohexylammonium salt
CAS号1566-15-0
分子式C10H24Cl2N3O2P
分子量320.196221
EINECS号
相关类别Amino Acids & Derivatives, Heterocycles, Metabolites & Impurities, Pharmaceuticals, Intermediates & Fine Chemicals
Mol文件1566-15-0.mol
结构式PHOSPHORAMIDEMUSTARD 结构式

PHOSPHORAMIDEMUSTARD 性质

熔点100-103°C
储存条件Hygroscopic, -20°C Freezer, Under inert atmosphere
溶解度可溶于氯仿(少许)、甲醇(少许)
形态固体
颜色白色至类白色
稳定性湿气敏感
InChI1S/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)
InChIKeyBGTIPRUDEMNRIP-UHFFFAOYSA-N
SMILESClCCN(P(N)(O)=O)CCCl.NC1CCCCC1

PHOSPHORAMIDEMUSTARD 用途与合成方法

Phosphoramide mustard cyclohexanamine 是环磷酰胺 (HY-17420) 的活性代谢物,具有抗肿瘤活性。Phosphoramide mustard cyclohexanamine 能诱导 DNA 损伤

Phosphoramide mustard cyclohexanamine causes cytotoxicity through forming cross-linked DNA adducts which inhibit DNA strand separation during replication.
Phosphoramide mustard cyclohexanamine (3-6 μM; 48 hours) reduces cell viability in rat spontaneously immortalized granulosa cells (SIGCs).
Phosphoramide mustard cyclohexanamine (3-6 μM; 24-48 hours) induces DNA adduct formation and ovarian DNA damage.
Phosphoramide mustard cyclohexanamine (3-6 μM; 24-48 hours) increases DNA damage responses (DDR) gene mRNA expression levels and DDR proteins.

Cell Viability Assay

Cell Line: SIGCs
Concentration: 0.5 μM, 1 μM, 3 μM, 6 μM
Incubation Time: 48 hours
Result: Reduced cell viability at concentrations of 3 μM and higher.

RT-PCR

Cell Line: SIGCs
Concentration: 3 μM, 6 μM
Incubation Time: 24 hours, 48 hours
Result: Increased DDR gene mRNA expression levels.

Western Blot Analysis

Cell Line: SIGCs
Concentration: 3 μM, 6 μM
Incubation Time: 24 hours, 48 hours
Result: Generally increased DDR proteins.

Phosphoramide mustard cyclohexanamine (2.1-20.7 mg/kg; i.p.; daily; for 5 days) inhibits subcutaneous tumor growth in rats.
Phosphoramide mustard cyclohexanamine exhibits terminal elimination half-lives (rat 15.1 min) following intravenous administration (rat 59.4 mg/kg).

Animal Model: Rat, subcutaneously implanted Walker 256 carcinosarcoma tumor
Dosage: 2.1 mg/kg, 4.8 mg/kg, 10.4 mg/kg, 20.7 mg/kg
Administration: Intraperitoneal injection, once daily, for 5 consecutive days
Result: Required to produce 50% inhibition of subcutaneous tumor growth with dose of 12 mg/kg.
Animal Model: Rats
Dosage: 86.0 mg/kg (Pharmacokinetic Analysis)
Administration: Intravenous injection
Result: T 1/2 (15.1 min).

安全信息

WGK GermanyWGK 3
存储类别11 - 可燃固体

MSDS信息

更新日期产品编号产品名称CAS号包装价格
2026/06/05HY-137316APhosphoramide mustard cyclohexanamine1566-15-01 mg1545元
2026/06/05HY-137316APHOSPHORAMIDEMUSTARD
Phosphoramide mustard (cyclohexanamine)
1566-15-05mg3400元

PHOSPHORAMIDEMUSTARD 上下游产品信息

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