首页工具

登录

搜索结果

Search Results for " cyclophosphamide "

如果没找到您满意的产品或者您对产品有其他要求，可以联系我们专业顾问为您提供针对性的合理建议。 QQ咨询网站留言咨询

Cat. No.	Product Name	Target	Signaling Pathways
T0707L	Cyclophosphamide	DNA Alkylator/Crosslinker; DNA; MRP	DNA Damage/DNA Repair; Immunology/Inflammation
	Cyclophosphamide 是一种烷化剂，具有抗肿瘤及免疫抑制活性，用于治疗多种癌症。
T0707	Cyclophosphamide hydrate 环磷酰胺一水物,Cyclophosphamide monohydrate,环磷酰胺水合物	DNA Alkylator/Crosslinker; DNA; MRP	DNA Damage/DNA Repair; Immunology/Inflammation
	Cyclophosphamide hydrate 是一种 DNA 烷化剂，一种 DNA 合成抑制剂。Cyclophosphamide hydrate 具有抗肿瘤活性、免疫抑制活性等。
T35643	4-hydroperoxy Cyclophosphamide 4-hydroperoxy Cyclophosphamide,4-OOH-CY
	4-hydroperoxy Cyclophosphamide (4-OOH-CY) is the active metabolite form of the prodrug Cyclophosphamide. 4-OOH-CY crosslinks DNA and induces T cell apoptosis independent of death receptor activation, but activates mitochondrial death pathways through production of reactive oxygen species (ROS).[1] Formulations containing the prodrug Cyclophosphamide are used to treat lymphomas and autoimmune disorders.[2],[3]
T35645	4-oxo Cyclophosphamide
	4-oxo Cyclophosphamide is an inactive metabolite of the alkylating agent cyclophosphamide .1,2It is formed from cyclophosphamide through a 4-hydroxycyclophosphamide intermediate by aldehyde dehydrogenases.2 1.Struck, R.F., Kirk, M.C., Mellett, L.B., et al.Urinary metabolites of the antitumor agent cyclophosphamideMol. Pharmacol.7(5)519-529(1971) 2.de Jonge, M.E., Huitema, A.D.R., Rodenhuis, S., et al.Clinical pharmacokinetics of cyclophosphamideClin. Pharmacokinet.44(11)1135-1164(2005)
T1414	Sodium 2-mercaptoethanesulfonate Mitexan,美司那,美司钠,Uromitexan,Mesna,Mesnum,Mesnex	Others	Others
	Sodium 2-mercaptoethanesulfonate (Uromitexan) 是一种抗氧化剂，具有细胞保护作用。它可用于减轻由环磷酰胺引起的出血性膀胱炎。它广泛用作抗化学疗法毒性的全身保护剂。
T38410	Phosphoramide mustard	DNA Alkylation; Drug Metabolite	DNA Damage/DNA Repair; Metabolism
	Phosphoramide mustard 是环磷酰胺的毒性代谢物物，具有抗癌活性且对卵巢具有毒性，可诱导 DNA 损伤。
T1055	Ifosfamide NSC109724,Isophosphamide,异环磷酰胺	DNA Alkylator/Crosslinker; DNA/RNA Synthesis	Cell Cycle/Checkpoint; DNA Damage/DNA Repair
	Ifosfamide (NSC-109724) 是一种烷化剂，具有抗肿瘤活性。它烷基化并形成 DNA 交联，从而防止 DNA 链分离和 DNA 复制。它是一种前药，必须通过肝微粒体酶的羟基化来激活。
T37108	Carboxyphosphamide
	Carboxyphosphamide is an inactive metabolite of the alkylating agent cyclophosphamide .1It is formed from cyclophosphamideviaoxidation of the intermediate metabolite aldophosphamide by aldehyde dehydrogenase. 1.Manthey, C.L., and Sladek, N.E.Kinetic characterization of the catalysis of activated" cyclophosphamide (4-hydroxycyclophosphamide/aldophosphamide) oxidation to carboxyphosphamide by mouse hepatic aldehyde dehydrogenasesBiochem. Pharmacol.37(14)2781-2790(1988)"
T29845	Alcophosphamide NSC 153182,Hydroxyphosphamide
	Alcophosphamide is a urinary metabolite of cyclophosphamide which may be used in proteomics research.
T24102	GR-203040 HCl GR 203040,GR-203040 hydrochloride,GR-203040,GR203040
	GR203040 inhibits cyclophosphamide-induced damage in the rat and ferret bladder. GR-203040 is a selective NK1 receptor antagonist.
T25723	L-Ifosfamide (+)-Ifosfamide
	L-Ifosfamide is nitrogen mustard, a chemotherapeutic antineoplastic, and more precisely an alkylating agent structural analog of cyclophosphamide with respect to which presents some differences regard to the antitumor activity and spectrum.
T68434	Mafosfamide
	Mafosfamide is a synthetic oxazaphosphorine derivative with antineoplastic properties. Mafosfamide alkylates DNA, forming DNA cross-links and inhibiting DNA synthesis. Although closely related to cyclophosphamide, mafosfamide, unlike cyclophosphamide, does not require hepatic activation to generate its active metabolite 4-hydroxy-cyclophosphamide; accordingly, mafosfamide is potentially useful in the intrathecal treatment of neoplastic meningitis.
T68592	Mafosfamide sodium
	Mafosfamide is a synthetic oxazaphosphorine derivative with antineoplastic properties. Mafosfamide alkylates DNA, forming DNA cross-links and inhibiting DNA synthesis. Although closely related to cyclophosphamide, mafosfamide, unlike cyclophosphamide, does not require hepatic activation to generate its active metabolite 4-hydroxy-cyclophosphamide; accordingly, mafosfamide is potentially useful in the intrathecal treatment of neoplastic meningitis.
T70304	CI-898 HCl
	CI-898 HCl is a lipophilic antifolate inhibitor of dihydrofolate reductase (DHFR). It has enhanced binding to DHFR in the presence of the cofactor NADPH. Cl-898 HCl inhibits cell growth and halts the cell cycle at the G1/S phase in L1210 mouse lymphocytic leukemia cells and is active against methotrexate-resistant cancer cell lines. It also enhances the activity of doxorubicin, cyclophosphamide, and 6-thioguanine (6-TG) in mice with advanced stage P338 leukemia.
T36701	Phosphoramide mustard (cyclohexanamine)
	Phosphoramide mustard cyclohexanamine is the major metabolite for Cyclophosphamide , with anticancer activitiy. Phosphoramide mustard cyclohexanamine induces DNA adduct formation in ovarian granulosa cells, induces DNA damage and elicits the ovarian DNA repair response[1][2]. Phosphoramide mustard cyclohexanamine causes cytotoxicity through forming cross-linked DNA adducts which inhibit DNA strand separation during replication[1].Phosphoramide mustard cyclohexanamine destroys rapidly dividing ce...
T63464	ERCC1-XPF-IN-1
	ERCC1-XPF-IN-1 是有效的、高亲和力的 ERCC1-XPF 抑制剂 (IC50: 0.49 μM)。ERCC1-XPF-IN-1 能够抑制 CPDs 的去除，降低环磷酰胺对结直肠癌细胞的毒性，提高了 UV 辐射的细胞毒性作用，阻碍 DNA 修复。
T71549	RKS-262
	RKS262 is a specific cyclin/CDK inhibitor. RKS262 was identified by structural optimization of Nifurtimox which is currently undergoing phase II clinical trials to treat high-risk neuroblastoma. In a NCI(60) cell-line assay RKS262 exhibited significant cytotoxicity in ovarian cancer cells and a variety of other cell lines exceeding effects of commercial drugs such as cisplatin, 5-FU, cyclophosphamide or sapacitabine. Various leukemia cell-lines were most sensitive (GI(50): ~ 10 nM) while several...

化合物

Cyclophosphamide

Cat.No: T0707L

Target: DNA Alkylator/Crosslinker, DNA, MRP

Cyclophosphamide hydrate

Cat.No: T0707

Synonym: 环磷酰胺一水物,Cyclophosphamide monohydrate,环磷酰胺水合物

Target: DNA Alkylator/Crosslinker, DNA, MRP

4-hydroperoxy Cyclophosphamide

Cat.No: T35643

Synonym: 4-hydroperoxy Cyclophosphamide,4-OOH-CY

4-oxo Cyclophosphamide

Cat.No: T35645

Sodium 2-mercaptoethanesulfonate

Cat.No: T1414

Synonym: Mitexan,美司那,美司钠,Uromitexan,Mesna,Mesnum,Mesnex

Target: Others

Phosphoramide mustard

Cat.No: T38410

Target: DNA Alkylation, Drug Metabolite

Cat.No: T1055

Synonym: NSC109724,Isophosphamide,异环磷酰胺

Target: DNA Alkylator/Crosslinker, DNA/RNA Synthesis

Carboxyphosphamide

Cat.No: T37108

Alcophosphamide

Cat.No: T29845

Synonym: NSC 153182,Hydroxyphosphamide

Cat.No: T24102

Synonym: GR 203040,GR-203040 hydrochloride,GR-203040,GR203040

Cat.No: T25723

Synonym: (+)-Ifosfamide

Cat.No: T68434

Mafosfamide sodium

Cat.No: T68592

Cat.No: T70304

Phosphoramide mustard (cyclohexanamine)

Cat.No: T36701

Cat.No: T63464

Cat.No: T71549

我们的所有产品和服务仅用于科学研究，不能被用于人体，我们也不向个人提供产品和服务。

Copyright © 2015-2024 TargetMol Chemicals Inc. All rights reserved. 沪ICP备20019793号-4

沪公网安备 31010602006700号

沪公网安备 31010602006700号

TargetMol Loading

联系我们

电话：

400-820-0310

邮箱：

service@tsbiochem.com

QQ：

2881945090（终端用户）

2885109491（经销商）

经销：

终端：

地址：

上海市静安区江场三路238号8楼