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Cat. No. | Product Name | Target | Signaling Pathways |
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T1564 |
Cisplatin
cis-Diaminodichloroplatinum,CDDP,顺铂 |
DNA Alkylator/Crosslinker; Ferroptosis; DNA/RNA Synthesis; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair |
Cisplatin (CDDP) 是一种 DNA 交联剂。Cisplatin 具有抗肿瘤活性,能够通过在癌细胞中形成 DNA 加合物来抑制 DNA 合成。Cisplatin 还可激活铁死亡并诱导自噬。 | |||
T19106 |
2-(Pyridyldithio)ethylamine hydrochloride
2-(2-吡啶基二硫基)乙胺盐酸盐,(S)-2-Pyridylthio Cysteamine Hydrochloride |
Others | Others |
2-(Pyridyldithio)ethylamine hydrochloride ((S)-2-Pyridylthio Cysteamine Hydrochloride) 是新型的二硫化物插入交联剂。 | |||
T1224 |
Cefuroxime sodium
Anaptivan,头孢呋辛钠,Cefuroxime sodium salt,Biociclin |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefuroxime sodium (Cefuroxime sodium salt) 是一种具有口服活性的头孢菌素抗生素,增加了对 β-内酰胺酶的稳定性。 | |||
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。 | |||
T14298 |
Rimiducid
|
Apoptosis; Others; Fatty Acid Synthase | Apoptosis; Metabolism; Others |
Rimiducid 是一种可渗透脂质的他克莫司类似物,是一种二聚剂,通过交联 FKBP 结构域起作用。它将 Caspase 9 自杀开关二聚化并迅速诱导细胞凋亡。 | |||
T78362 |
Transglutaminase
TG |
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Transglutaminase (TG) 是一种硫醇酶,促使蛋白质分子间交联,通过催化谷氨酰胺残基的γ-羧酰胺基团与其他化合物的一级ε-胺基团形成异肽键。该酶在包括凝血、抗菌免疫反应和光合作用在内的多种生理过程中发挥作用。 | |||
T5022 |
Ceforanide
|
Antibacterial; Antibiotic | Microbiology/Virology |
Ceforanide 是一种头孢菌素,可静脉或肌肉给药。它在体外具有一系列抗菌活性。 | |||
T21306 |
Glyfosfin
|
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Glyfosfin is a DNA cross-linking agent and an alkylating agent with anticancer activity. | |||
T32206 |
Isodityrosine
|
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Isodityrosine is a new cross-linking amino acid from plant cell-wall glycoprotein. | |||
T16890 |
SJG-136
NSC-694501 |
Others | Others |
SJG-136 is a DNA cross-linking agent (XL50: 45 nM for pBR322 DNA). | |||
T35271 |
Yoshi-864
Yoshi864,Improsulfan HCl,NSC102627,Improsulfan hydrochloride |
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Yoshi-864 alkylates and cross-links DNA, thereby inhibiting DNA replication. It is an alkyl sulfonate DNA cross-linking agent with potential anti-cancer activity. | |||
T41026 |
Biotin-LC-LC-NHS
|
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Biotin-LC-LC-NHS is a SMCC cross-linking reagent, which serves as a labeling agent for antibodies and small molecules, like Paclitaxel. | |||
T19944 |
DSSeb Crosslinker
DSSeb Cross linker,DSSeb Cross-linker |
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DSSeb Crosslinker is a homobifunctional cross-linking reagent. It is useful in protein crosslinking and making antibody-drug conjugates. | |||
T40642 |
Chlorpyrifos-oxon
|
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Chlorpyrifos-oxon, an active metabolite of Chlorpyrifos, is a powerful phosphorylating agent with potent inhibition of AChE activity. It induces cross-linking between tubulin subunits and disrupts microtubule function[4]. | |||
T19568 |
Sulfo-SMPB sodium
|
Others | Others |
Sulfo-SMPB sodium is a non-cleavable heterobifunctional chemical cross-linking reagent that combines N-hydroxysuccinimide ester and maleimide groups. This compound enables the covalent conjugation of molecules possessing amine and sulfhydryl functionalities. | |||
T19945 |
N,N'-Carbonyldiimidazole
1,1'-Carbonyldiimidazole,N,N'-Carbonyldiimidazole,CDI Crosslinker |
Others | Others |
N,N'-Carbonyldiimidazole 是一种生物交联剂,在质谱检测化合物纯度上有很大的应用。 | |||
T19203 |
Bendamustine D4
SDX-105 D4 |
Others | Others |
Bendamustine D4 is the deuterium-labeled Bendamustine. Bendamustine is a DNA cross-linking compound with alkylating and antimetabolite properties. Bendamustine causes DNA breaks. | |||
T38765 |
UBE2T/FANCL-IN-1
UBE2T/FANCL-IN-1 |
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UBE2T/FANCL-IN-1 is a highly effective inhibitor of UBE2T/FANCL-mediated FANCD2 monoubiquitylation. It greatly enhances the sensitivity of cells to Carboplatin, a DNA cross-linking agent. | |||
T40947 | PR-104 sodium | ||
PR-104 sodium is a hypoxia-activated DNA cross-linking agent used in the research of tumor xenograft models. It functions as a nitrogen mustard pre-prodrug and efficiently transforms into the more lipophilic dinitrobenzamide mustards alcohol PR-104A. | |||
T71034 |
Bizelesin
|
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Bizelesin is a synthetic cyclopropylpyrroloindole antineoplastic antibiotic. Bizelesin binds to the minor groove of DNA and induces interstrand cross-linking of DNA, thereby inhibiting DNA replication and RNA synthesis. Bizelesin also enhances p53 and p21 induction and triggers G2/M cell-cycle arrest, resulting in cell senescence without apoptosis. | |||
T82466 |
Englumafusp alfa
RG6076,CD19-4-1BBL,RO7227166 |
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Englumafusp alfa (CD19-4-1BBL; RO7227166)是一款由CD19特异性抗体域与人41BBL的三聚体胞外域结合构成的融合蛋白。该化合物能够促进T细胞与NK细胞表面CD19特异性4-1BB的交联作用。 | |||
T69873 |
Cefdinir monohydrate
|
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Cefdinir monohydrate is the salt form of Cefdinir (free base), a semi-synthetic cephalosporin and a beta-lactam antibiotic with bactericidal activity. Cefdinir's effect is dependent on its binding to penicillin-binding proteins (PBPs) located in the bacterial cytoplasmic membrane. Binding results in the inhibition of the transpeptidase enzymes, thereby preventing cross-linking of the pentaglycine bridge with the fourth residue of the pentapeptide and interrupting consequent synthesis of peptidog... | |||
T81773 |
Modotuximab
Sym 004,DS 1024 |
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Modotuximab (Anti-HumanEGFRRecombinant Antibody) 是一种IgG1κ型嵌合抗体,靶向人源EGFR蛋白。由Futuximab部分构成,Modotuximab能同时结合EGFR上两个独立非重叠的表位。该抗体通过促进EGFR在细胞表面的交联,并加速EGFR的细胞内化与降解,展现出体内的抗肿瘤活性。 | |||
T35646 |
4-oxo-2-Nonenal
4-oxo-2-Nonenal,4-ONE |
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4-hydroxy Nonenal is a lipid peroxidation product derived from oxidized ω-6 polyunsaturated fatty acids such as arachidonic acid and linoleic acid. [1] [2] It exhibits various biological activities such as cytotoxicity, growth inhibiting activity, genotoxicity, and chemotactic activity and has been widely used as a marker of lipid peroxidation.[1][2][3] 4-oxo-2-Nonenal is a more recently identified product of lipid peroxidation.[4][5][6] It actively modifies histidine and lysine residues on prot... | |||
T62582 |
WEHI-150
|
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WEHI-150是一种米托蒽醌类似物,作为DNA链间交联剂,具有12.5小时的半衰期。该化合物能够在CpG序列上形成共价加合物,对甲基化CpG位点表现出选择性。甲醛激活的WEHI-150能够诱导DNA链间交联,并表现出浓度依赖性的转录阻断作用。此外,WEHI-150还能在新的DNA序列中形成加合物,这不涉及与鸟嘌呤N-2的相互作用。 | |||
T60438 |
PXS-6302
|
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PXS-6302 是不可逆的赖氨酸氧化酶 (LOX) 抑制剂,对Bovine LOX、rh LOXL1、rh LOXL2、rh LOXL3、rh LOXL4的IC50分别为 3.7 μM,3.4 μM,0.4 μM,1.5 μM 和0.3 μM。PXS-6302 可以轻松渗透皮肤,减少胶原蛋白沉积和交联,显着改善疤痕外观而不降低组织强度。 PXS-6302 在其他纤维化疾病中也可能有更广泛的应用。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN4345 |
Jacobine
|
Others | Others |
Jacobine induces significant dose-dependent DNA-DNA interstrand cross-linking over the entire range of doses. It was catalyzed by guinea pig hepatic glutathione-S-transferase enzymes in in vitro experiments. |