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Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7545 |
6-Aminonicotinamide
|
Others | Others |
6-Aminonicotinamide 是一种竞争性 NADP+依赖性酶,是一种烟酰胺抗代谢药,葡萄糖 6-磷酸脱氢酶抑制剂 (Ki=0.46 μM)。 它干扰糖酵解,导致 ATP 耗竭,并与 DNA 交联化学疗法药物,如Cisplatin,协同杀死癌细胞。 | |||
T35648 |
4-Thiouridine
|
Others | Others |
4-Thiouridine (4-TU) 是一种光活化核糖核苷类似物,广泛用于RNA 分析。 | |||
T19958 |
2-Iminothiolane HCl
2-Iminothiolane,2-亚氨基硫烷盐酸盐,Traut's reagent,Trauts reagent,2-IT |
Others | Others |
2-Iminothiolane HCl (Trauts reagent) 可用于将巯基引入衍生自天冬酰胺连接聚糖的寡糖中。 | |||
T1616 |
Cefotiam hydrochloride
盐酸头孢替安,Pansporin,SCE-963 hydrochloride,Pansporine,头孢替安盐酸盐,Cefotiam dihydrochloride,Halospor |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefotiam hydrochloride (SCE-963 hydrochloride) 是一种肠外头孢菌素类广谱抗生素,对革兰氏阳性菌和革兰氏阴性菌有活性。 | |||
T14061 |
EMCS
6-Maleimidohexanoic acid N-hydroxysuccinimide ester |
Others | Others |
EMCS (6-Maleimidohexanoic acid N-hydroxysuccinimide ester) 是一种异双官能团交联剂,是一种制备半抗原结合物和酶免疫偶联物的化合物,是抗体药物偶联物中一种有效的保护基团。 | |||
T4047 |
Bisantrene
CL216942,比生群 |
Topoisomerase | DNA Damage/DNA Repair |
Bisantrene (CL216942) 是一种具有抗肿瘤活性的蒽基双腙,可靶向作用于真核生物的 II 型拓扑异构酶。它插入并破坏 DNA 的构型,导致 DNA 单链断裂、DNA-蛋白质交联和 DNA 复制的抑制。 | |||
T5024 |
Cefotiam Hexetil Hydrochloride
盐酸头孢替安酯,头孢替安海替酯盐酸盐 |
Antibacterial; Antibiotic | Microbiology/Virology |
Cefotiam hexetil hydrochloride 是一种可口服头孢菌素,是抗生素 cefotiam 的前药,但无抗菌作用。 | |||
T4657 |
WHI-P97
4-(3',5'-二溴-4-羟基苯基)氨基-6,7-二甲氧基喹唑啉 |
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
WHI-P97 是一种选择性 JAK-3抑制剂,可用于预防过敏性哮喘的研究。 | |||
T38951 |
Isatuximab
SAR-650984,hu38SB19,Isatuximab-irfc |
Apoptosis; CD38 | Apoptosis; Immunology/Inflammation |
Isatuximab 是一种在血液系统恶性细胞中靶向跨膜受体和胞外酶 CD38 的单克隆抗体,是在多发性骨髓瘤中高度表达的蛋白。Isatuximab 具有抗肿瘤活性、抗体依赖性细胞介导的细胞毒性、补体依赖性细胞毒性、抗体依赖性细胞吞噬作用,可在无交联情况下直接诱导细胞凋亡 (apoptosis)。Isatuximab 对 CD38 胞外酶活性有抑制作用,这与许多细胞功能有关。 | |||
T38294 |
4-Deoxypyridoxine hydrochloride
|
S1P Receptor | GPCR/G Protein |
4-Deoxypyridoxine hydrochloride 通过抑制 S1P 裂解酶 (SPL) 活性来抑制细胞内 S1P 的降解,与 S1P 一样,减少化学诱导的胰岛素瘤细胞系的细胞凋亡。 | |||
T39757 |
EC2629
EC2629 |
||
EC2629 is a highly potent folate- receptor-targeted DNA crosslinking agent. | |||
T19560 |
SGD-1882
PBD dimer |
Others | Others |
SGD-1882 is a agent of cytotoxic, DNA minor-groove crosslinking pyrrolobenzodiazepine (PBD) dimer, and acting as the payload for ADCs. | |||
T19941 |
MBS Crosslinker
MBS protein crosslinker |
||
MBS crosslinker is a non-cleavable, water-insoluble, heterobifunctional protein crosslinking reagent. The MBS protein crosslinker extended spacer arm analog is SMPB crosslinker SATA Protein Modifier can be used to add sulfhydryl groups to proteins or pept | |||
T24841 |
Sulfo-MBS Crosslinker
Sulfo-MBS Cross linker,Sulfo-MBS Cross-linker |
||
Sulfo-MBS Crosslinker is a non-cleavable, water-soluble, heterobifunctional protein crosslinking reagent. It is commonly used to crosslink haptens to carrier proteins and enzymes to antibodies. | |||
T29964 |
Ametantrone Acetate
CI-881 |
||
Ametantrone Acetate is a topoisomerase II inhibitor of anthrapyrazole family, which can lead to DNA covalent crosslinking. | |||
T31584 |
DST Crosslinker
DST Cross linker,DST Cross-linker |
||
DST crosslinker(disuccinimide tartarate) is an isotype bifunctional, cleavable crosslinker (cleavable by an oxidizer) for applications that require crosslinking cleavability and that do not interfere with protein disulfide bonds with reducing agents. | |||
T19193 |
Amotosalen hydrochloride
S-59 |
Others | Others |
Amotosalen hydrochloride (S-59) is a light-activated, RNA-, DNA-crosslinking psoralen compound and is used to neutralize pathogens. | |||
T30598 |
BS2G-d4 Deuterated Crosslinker
D4-BS2G,BS2G-d4 |
||
BS2G-d4 or Bis(Sulfosuccinimidyl) 2,2,4,4-glutarate-d4, is a water-soluble and membrane impermeable protein crosslinking agent. | |||
T19942 |
SBA Crosslinker
SBA Cross-linker,SBA Cross linker |
||
SBA crosslinker is a sulfhydryl and amino reactive heterobifunctional protein crosslinking reagent. SBA protein crosslinker is non-cleavable and is among the shortest amine and sulfhydryl reactive crosslinking reagents known with a spacer arm length of on | |||
T24453 |
Metamelfalan
NSC-67781,Metamelfalanum,NSC67781,NSC 67781,m-L-Sarcolysin |
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Metamelfalan is an alkylating nitrogen mustard with potential antineoplastic activity. It causes crosslinking of DNA, thereby preventing DNA replication and eventually cellular proliferation. | |||
T19944 |
DSSeb Crosslinker
DSSeb Cross linker,DSSeb Cross-linker |
||
DSSeb Crosslinker is a homobifunctional cross-linking reagent. It is useful in protein crosslinking and making antibody-drug conjugates. | |||
T30599 |
BS3-d4 Deuterated Crosslinker
Deuterated Crosslinker BS3-d4,BS3-d4,D4-BS3 |
||
BS3-d4 Deuterated Crosslinker or Bis(Sulfosuccinimidyl) 2,2,7,7-suberate-d4, is a water-soluble and membrane impermeable protein crosslinking agent. | |||
T19943 |
SMPB Crosslinker
SMPB Cross linker,SMPB Cross-linker |
||
SMPB crosslinker is a heterobifunctional protein crosslinking reagent that is reactive toward sulfhydryl and amino groups. The SMPB protein crosslinker is an extended chain length analog of MBS crosslinker. SMPB crosslinker's spacer arm is non-cleavable. | |||
T61870 |
(rel)-Oxaliplatin
|
||
(rel)-Oxaliplatin is a DNA synthesis inhibitor that induces DNA crosslinking damage, inhibits DNA replication and transcription, and stimulates apoptosis. This compound has applications in cancer research [1] [2] [3]. | |||
T33490 |
m-PEG12-aldehyde
|
||
m-PEG12-aldehyde is a PEG derivative containing an aldehyde group. Aldehyde is reactive to hydrazide and aminooxy groups which are commonly used in biomolecular probes for labeling and crosslinking carbonyls (oxidized carbohydrates). The hydrophilic PEG s | |||
T16025 |
SGD-1910
MC-Val-Ala-PBD |
Others | Others |
MC-Val-Ala-PBD is a drug-linker conjugate for ADC by using the antitumor antibiotic, pyrrolobenzodiazepine (PBD, a cytotoxic DNA crosslinking), linked via the cleavable linker MC-Val-Ala[1]. | |||
T21134 |
Decane, 1,10-diiodo-
Decamethylene diiodide,1,10-Diiododecane |
||
Decane, 1,10-diiodo- is used as a crosslinking reagent for tetrabutylammonium polygalacturonic acid and as an alkylating agent in the synthesis of symmetrical and unsymmetrical bis-cryptophanes. It is also used to produce decane at temperature of 20°C. | |||
T79196 |
4-Thiouridine 5′-triphosphate tetralithium
4-Thio-UTP tetralithium |
P2Y Receptor | GPCR/G Protein; Neuroscience |
4-Thiouridine 5’-triphosphate (4-Thio-UTP) tetralithium 作为P2Y2和P2Y4受体的高效激动剂,其对hP2Y2的EC50为35 nM,对hP2Y4的EC50为350 nM。该化合物广泛应用于交联实验以及转录复合物标记研究。 | |||
T70229 |
Laromustine
|
||
Laromustine is a sulfonyl hydrazine prodrug with antineoplastic activity. Laromustine releases the DNA chloroethylating agent 90CE after entering the blood stream; 90CE chloroethylates alkylates the 06 position of guanine, resulting in DNA crosslinking, strand breaks, chromosomal aberrations, and disruption of DNA synthesis. Intracellular metabolism of this agent also releases methyl isocyanate which inhibits 06-alkyl-guanine transferase, an enzyme involved with DNA repair. | |||
T79197 |
4-Thiouridine 5′-triphosphate tetrasodium
4-Thio-UTP tetrasodium |
P2Y Receptor | GPCR/G Protein; Neuroscience |
4-Thiouridine 5′-triphosphate (4-Thio-UTP) tetrasodium 作为P2Y2和P2Y4受体的有效激动剂,显示出对hP2Y2的EC50为35 nM,以及对hP2Y4的EC50为350 nM。该化合物适用于交联实验和转录复合物标记研究。 | |||
T77238 |
Fmoc-L-photo-proline
|
||
Fmoc-L-photo-proline为可通过Fmoc固相法纳入合成肽中的光交联氨基酸。该化合物在环状拟肽抗生素合成及肽基光亲和探针研究制备中应用广泛。 | |||
T36745 |
cDPCP
|
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cDPCP is a platinum-containing DNA-crosslinking agent.1Unlike cisplatin or oxaliplatin , cDPCP forms monofunctional DNA adducts. It is transported into cells by organic cation transporter 1 (OCT1) and OCT2, inhibiting proliferation of MDCK cells expressing the human transporters with IC50values of 8.1 and 1.5 μM, respectively. cDPCP inhibits RNA polymerase II-mediated transcription in a reporter assay using HeLa cells. It increases survival in murine S180 sarcoma and P388 leukemia models when ad... | |||
T12585L |
PXS-5153A monohydrochloride
PXS-5153A monohydrochloride (2125956-82-1 free base) |
Others | Others |
PXS-5153A monohydrochloride 是一种有效的、选择性的、具有口服活性和快速起效的赖氨酰氧化酶 2/3(LOXL2/LOXL3)的双抑制剂,对几乎所有哺乳动物物种 LOXL2的 IC50均< 40 nM,对人类 LOXL3 的 IC50为63 nM。PXS-5153A monohydrochloride 可减少交联并改善纤维化。 | |||
T71401 | Oxaliplatin-d10 | ||
Oxaliplatin-d10 is intended for use as an internal standard for the quantification of oxaliplatin by GC- or LC-MS. Oxaliplatin is a platinum-containing DNA-crosslinking agent. It induces the formation of DNA inter- and intrastrand crosslinks and DNA-protein adducts, inhibits DNA and RNA synthesis, and induces apoptosis in cancer cells. Oxaliplatin is cytotoxic to cisplatin-sensitive A2780(1A9) and KB-3-1 cells and cisplatin-resistant A2780-E(80) and KB-CP20 cells (IC50s = 0.12, 0.39, 4.7, and 2.... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2210 |
Genipin
京尼平,(+)-Genipin |
Others; Autophagy | Autophagy; Others |
Genipin ((+)-Genipin) 是衍生自黄栀果实的天然交联剂,可抑制细胞中的 UCP2 (解偶联蛋白 2)。它有蛋白质调节、抗肿瘤、抗炎症、免疫抑制、抗血栓形成和对海马神经元保护的多种生物活性,可研究 2 型糖尿病。 | |||
T4704 |
L-Anserine nitrate
L-鹅肌肽硝酸盐,L-Anserine nitrate salt |
Others; Endogenous Metabolite | Metabolism; Others |
L-Anserine nitrate (L-Anserine nitrate salt) 是一种存在于大多数动物组织中的二肽。在模型系统中,它是一种有效的抗氧化剂和羟基自由基清除剂。该化合物抑制醛糖和酮糖还原糖诱导的非酶蛋白糖基化。 |