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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T8897 |
2-Iodoacetamide
碘乙酰胺,2-碘乙酰胺,Iodoacetamide |
Others | Others |
2-Iodoacetamide (Iodoacetamide) 是常用的烷基化剂之一,能够在蛋白质组学样品制备过程中,将半胱氨酸烷基化。 | |||
T8380 |
Bendamustine
SDX105,宾达氮芥 |
Apoptosis; Others; DNA Alkylator/Crosslinker | Apoptosis; DNA Damage/DNA Repair; Others |
Bendamustine (SDX105) 是一种嘌呤类似物,是一种 DNA 交联剂,具有烷基化、抗癌和抗代谢作用。它可激活 DNA 损伤反应和细胞凋亡。 | |||
T4169 |
N-Nitroso-N-methylurea
1-甲基-1-亚硝基脲,1-Methyl-1-nitrosourea,N-Methyl-N-nitrosourea,Methylnitrosourea |
Others; DNA Alkylator/Crosslinker | DNA Damage/DNA Repair; Others |
N-Nitroso-N-methylurea (Methylnitrosourea) 是一种具有烷基化、致癌和致突变特性的亚硝基脲化合物。它靶向多种动物器官,可引起各种癌症和变性疾病,可用于重氮甲烷合成。 | |||
T0095 |
Bendamustine hydrochloride
SDX-105,SDX-105 (Cytostasane) HCl,Bendamustine HCl,EP-3101,盐酸苯达莫司汀 |
Apoptosis; DNA Alkylator/Crosslinker; DNA/RNA Synthesis | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Bendamustine hydrochloride (EP-3101) 是一种嘌呤类似物,是一种 DNA 交联剂。它可激活 DNA 损伤反应和细胞凋亡,有烷基化,抗癌和抗代谢作用。 | |||
T1250 |
Thio-TEPA
Tiofosyl,Triethylenethiophosphoramide,三亚乙基硫代磷酰胺,Tiofosfamid |
DNA Alkylator/Crosslinker; DNA Alkylation; Antibacterial; Antibiotic | DNA Damage/DNA Repair; Microbiology/Virology |
Thio-TEPA (Tiofosyl) 是一种具有抗肿瘤作用的 DNA 烷化剂。 | |||
T1601 |
Lomustine
CCNU,NSC 79037,洛莫司汀 |
Apoptosis; Others; DNA Alkylator/Crosslinker; DNA Alkylation; Autophagy | Apoptosis; Autophagy; DNA Damage/DNA Repair; Others |
Lomustine (NSC-79037) 是一种具有抗肿瘤活性的 DNA 烷化剂。 | |||
T26978 |
CEP-40125
RXDX-107 |
DNA Alkylation | DNA Damage/DNA Repair |
CEP-40125 (RXDX-107) 是一种 DNA 烷基剂,可用于研究晚期实体瘤。 | |||
T1241 |
Altretamine
Hexamethylmelamine,NSC13875,六甲蜜胺,RB-1515,ENT-50852,WR-95704 |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Altretamine (ENT-50852) 是一种具有抗肿瘤活性的烷化剂。 | |||
T19736 |
Aniline mustard
Mesylerythrol,NSC-18429,N,N-双(2-氯乙基)苯胺,Lymphocin |
Others | Others |
Aniline mustard (Mesylerythrol) 是具有抗肿瘤活性的烷基化芥末。 | |||
T17159 |
Treosulfan
NSC 39069,曲奥舒凡,Treosulphan |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Treosulfan (Treosulphan) 是一种双功能的烷化剂,对卵巢癌及其他的实体瘤都有抑制效果。 | |||
T3091 |
Carmustine
bis-chloroethylnitrosourea,Nitrumon,卡莫司汀,Gliadel,BCNU,BiCNU,Carmubris |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Carmustine (bis-chloroethylnitrosourea) 是一种细胞周期性非特异性烷基化抗肿瘤剂。 | |||
T13689 |
Ethylene dimethanesulfonate
|
Apoptosis | Apoptosis |
Ethylene dimethanesulfonate 是温和的烷基化乙二醇非挥发性甲烷磺酸二酯,对 LC 具有选择性的促凋亡作用。 | |||
T17212 |
VAL-083
1,2:5,6-二脱水半乳糖醇,Dianhydrogalactitol,去水卫矛醇,Dianhydrodulcitol |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
VAL-083 (Dianhydrogalactitol) 是一种烷化剂,具有抗肿瘤活性,可在 DNA 上产生 N7 甲基化。 | |||
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。 | |||
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。 | |||
T16871 |
Semustine
|
DNA Alkylator/Crosslinker | DNA Damage/DNA Repair |
Semustine 是一种 DNA 烷化剂,是一种癌症化疗化合物,在接受辅助化疗的恶性黑色素瘤患者中具有肾毒性,可用于辅助治疗白血病。 | |||
T21463 |
Temozolomide Acid
TMZA,3,4-二氢-3-甲基-4-氧代咪唑并[5,1-D]-1,2,3,5-四嗪-8-甲酰胺酸 |
Others | Others |
Temozolomide Acid (TMZA) 是 temozolomide (TMZ) 的代谢物。TMZ 在体外具有抗癌活性。TMZ 是一种口服烷化剂,用于治疗多形性胶质母细胞瘤 (GBM) 和星形细胞瘤。 | |||
T28663 |
Sarmustine
NSC-364432,SarCNU,Sarcosinamide,NSC 364432,NSC364432 |
||
Sarmustine (SarCNU) 是一种具有抗癌活性的烷化剂,通过 p53 依赖性和 p53 非依赖性途径抑制前列腺癌细胞的生长。Sarmustine 在体外介导 P140K 甲基鸟嘌呤-DNA-甲基转移酶转导的人 CD34(+)细胞的选择。 | |||
T0164 |
Oxaliplatin
L-OHP,奥沙利铂 |
DNA Alkylator/Crosslinker; DNA/RNA Synthesis; Autophagy | Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Oxaliplatin (L-OHP) 是一种 DNA 烷化剂,一种 DNA 合成抑制剂。Oxaliplatin 会导致 DNA 交联损伤,阻止 DNA 复制和转录并导致细胞死亡。Oxaliplatin 可以诱导细胞自噬。 | |||
T1178 |
Temozolomide
NSC 362856,替莫唑胺,TZM,CCRG 81045,TMZ |
Apoptosis; DNA Alkylator/Crosslinker; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Temozolomide (TMZ) 是一种 DNA 烷基化剂,具有血脑屏障渗透性和口服活性。Temozolomide 具有抗肿瘤活性和抗血管生成活性,还可以诱导细胞凋亡和自噬。 | |||
T15771 |
Lobaplatin
D-19466,络铂 |
DNA Alkylation | DNA Damage/DNA Repair |
Lobaplatin (D-19466) 是一种铂 (II) 复合物的非对映混合物,是一种有前途的抗肿瘤化疗药物,在多种肿瘤类型的患者中具有活性。 | |||
T4469 |
Nemorubicin
Methoxymorpholinyldoxorubicin,PNU-152243A,PNU 152243,奈莫柔比星 |
Others | Others |
Nemorubicin (PNU 152243) 是一种 Doxorubicin 衍生物,具有抗肿瘤活性。它需要完整的核苷酸切除修复系统才能发挥活性。它对多药耐药表型的多种肿瘤细胞系具有细胞毒性。 | |||
T61487 |
APE1-IN-1
|
DNA/RNA Synthesis | Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
APE1-IN-1 是一种可透过血脑屏障且有效的无嘌呤/嘧啶内切酶 1 (APE1) 抑制剂,具有潜在的抗肿瘤活性,可增强烷基化剂甲基甲烷磺酸盐对癌细胞的细胞毒性。 | |||
T6798 |
Tretazicar
5-Aziridino-2,4-dinitrobenzamide,CB1954,NSC 115829 |
DNA Alkylator/Crosslinker; DNA Alkylation | DNA Damage/DNA Repair |
Tretazicar (NSC-115829) 是一种抗肿瘤前药,由 NAD(P)H 醌氧化还原酶 2 激活。它在酶促活化后生成细胞毒性双功能烷基剂,可以形成 DNA-DNA 链间交联。 | |||
T21320 |
Methoxyamine HCl
甲氧基胺盐酸盐,TRC102,TRC 102,Methoxyamine,TRC-102 |
Others | Others |
Methoxyamine HCl (Methoxyamine) 与脱嘌呤/脱嘧啶 (AP) DNA 损伤位点共价结合并抑制碱基切除修复 (BER),这可能导致 DNA 链断裂和细胞凋亡增加。 Methoxyamine 是一种具有潜在佐剂活性的口服生物可利用的小分子抑制剂。该药剂可增强烷化剂的抗肿瘤活性。 | |||
T3615 |
Evofosfamide
艾伏磷酰胺,TH-302 |
Apoptosis; Others | Apoptosis; Others |
Evofosfamide (TH-302) 是一种缺氧激活前药,在缺氧 (N2) 和常氧 (21% O2) 环境下,IC50分别为 10 μM 和 1000 μM。 | |||
T4570 |
Pipobroman
Vercyte,A-8103,Amedel,哌泊溴烷 |
Others; DNA Alkylator/Crosslinker | DNA Damage/DNA Repair; Others |
Pipobroman (Vercyte) 是一种烷基化剂,是哌嗪的溴化衍生物。它通过抑制 DNA 和 RNA 聚合酶或减少嘧啶核苷酸掺入 DNA 发挥其作用。它在真性红细胞增多症和原发性血小板增多症中具有良好的临床活性,可用于癌症研究。 | |||
T21306 |
Glyfosfin
|
||
Glyfosfin is a DNA cross-linking agent and an alkylating agent with anticancer activity. | |||
T11046 |
Dimethyl-SGD-1882
Dimethyl-PBD dimer |
Others | Others |
Dimethyl-SGD-1882 (Dimethyl-PBD dimer) is a highly efficient DNA alkylating agent used as antibody-drug conjugate (ADC) cytotoxin. PBD Dimer is a DNA alkylating agent that inhibits DNA replication. | |||
T34424 |
RSU 1164
RSU-1164,RSU1164 |
||
RSU 1164 is an electron affinic agent that contains a nitro group and a weakly basic alkylating aziridine moiety. | |||
T12586 | Py-MPB-amino-C3-PBD | Others | Others |
Py-MPB-amino-C3-PBD is a cytotoxic agent comprised non-alkylating group,with antimicrobial activity. | |||
T68622 |
Ditiomustine
|
||
Ditiomustine is a nitrosourea compound with alkylating activity. Ditiomustine crosslinks DNA, resulting in the inhibition of DNA replication and eventually cellular proliferation. It was developed as antineoplastic agent. | |||
T34474 |
S-23906-1
S239061 |
||
S-23906-1 is a potential alkylating agent for solid tumors. | |||
T34927 |
Triaziquone
Trenimone,A 163,Trenimon |
||
Triaziquone is an alkylating agent that can react with DNA to form intrastrand crosslinks. | |||
T41074 |
MB-VC-MGBA
|
||
MB-VC-MGBA is a potent antitumor drug-linker conjugate for antibody-drug conjugates (ADC), utilizing the minor-groove-binding DNA-alkylating agent (MGBA), connected through the ADC linker MB-VC. | |||
T21133 |
Decane, 1,10-dibromo-
Decamethylene dibromide,1,10-Dibromodecane |
||
Decane, 1,10-dibromo- is used as synthetic organic intermediate and as an alkylating agent. | |||
T24453 |
Metamelfalan
NSC-67781,Metamelfalanum,NSC67781,NSC 67781,m-L-Sarcolysin |
||
Metamelfalan is an alkylating nitrogen mustard with potential antineoplastic activity. It causes crosslinking of DNA, thereby preventing DNA replication and eventually cellular proliferation. | |||
T32376 | Kenazepine | ||
Kenazepine is a benzodiazepine cpd containing functional alkylating moiety. | |||
T72217 |
Altretamine hydrochloride
RB-1515 hydrochloride,ENT-50852 hydrochloride ; RB-1515 hydrochloride ; WR-95704 hydrochloride,ENT-50852 hydrochloride,WR-95704 hydrochloride |
||
Altretamine hydrochloride 是一种烷化剂 (alkylator),具有抗肿瘤活性。 | |||
T25299 |
Degranol
NSC 9698,NSC-9698,NSC9698 |
||
Degranol is a nitrogen mustard derivative alkylating agent utilized as antineoplastic. It causes severe bone marrow depression and is a powerful vesicant. | |||
T68715 |
Anaxirone
|
||
Anaxirone is a synthetic triepoxide alkylating agent with potential antineoplastic activity. Anaxirone alkylates DNA via actual or derived epoxide groups, resulting in inhibition of DNA synthesis. This agent has been shown to exhibit a broad spectrum of antineoplastic activity against experimental tumors, including those resistant to other alkylating agents. | |||
T10974 |
DC41
|
Others | Others |
DC41 is a derivative of DC1. DC1 is a simplified analogue of CC-1065, an antibody conjugate of cytotoxic DNA alkylating agents, used for targeted treatment of cancer. | |||
T28418 |
Piposulfan
Ancyte,A-20968,A 20968,A20968 |
||
Piposulfan, a water-insoluble alkylating agent, is used as an antineoplastic and anti-tumor agent. | |||
T34523 |
Sarcolysine hydrochloride
DL-Phenylalanine mustard hydrochloride,Melphalan,DL-Sarcolysine hydrochloride,DL-Sarcolysin monohydrochloride,AI3-52155,Alkeran |
||
Sarcolysine hydrochloride, also known as Melphalan HCl, is a nitrogen mustard and alkylating agent that has been studied for use in multiple myeloma therapy. | |||
T25816 |
Mitolactol
NSC 104800,NSC-104800,NSC104800 |
||
Mitolactol is an alkylating antineoplastic toxic to bone marrow; utilized in breast cancer, also in combination with other drugs. Mitolactol is able to cross bloodbrain barrier, consequently could control certain brain tumors. | |||
T29851 |
Aldoifosfamide
UNII-S1JX147O5E,Mitoxana,Ifex |
||
Aldoifosfamide is a metabolite of ifosfamide. Ifosfamide (also marketed as Mitoxana and Ifex) is a nitrogen mustard alkylating agent used in the treatment of cancer. It is sometimes abbreviated 'IFO''. | |||
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)" | |||
T11116 |
Duocarmycin MA
|
Others | Others |
Duocarmycin MA can be used against multi-drug resistant cell lines.Duocarmycin MA is an antibody drug conjugates (ADCs) toxin. Duocarmycin is a DNA alkylating agent that binds in the minor groove. | |||
T22388 | OBI-3424 | Others | Others |
OBI-3424, a highly selective prodrug, is converted by aldo-keto reductase family 1 member C3 (AKR1C3) to a potent DNA-alkylating agent. | |||
T11119 |
Duocarmycin DM free base
Duocarmycin |
Others | Others |
Duocarmycin is a DNA minor groove binding alkylating agent and explored as drug–antibody conjugates (ADCs) . Duocarmycin is based on its characteristic curved indole structure and a spirocyclopropylcyclohexadienone electrophile to act anticancer activity. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T15467 |
Helenalin
|
Others | Others |
Helenalin is a selective inhibitor of transcription factor NF-κB by direct targeting of p65. It is an anti-inflammatory sesquiterpene lactone compound with alkylating activity. Through its ability to target the cysteine sulfhydryl groups in the p65 subunit of NF-κB, helenalin effectively inhibits its DNA binding. |