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5
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T16251 |
N-Succinimidyl-S-acetylthioacetate
SATA,N-丁二酸,S-乙酰基巯基乙二醇酯 |
Others | Others |
N-Succinimidyl-S-acetylthioacetate (SATA) 是蛋白质修饰剂,它能够以受保护的形式将巯基添加到蛋白质和其他含胺分子中。 | |||
T19780 |
2,2′-Dipyridyl disulfide
2,2'-Dipyridyl disulfide,OPSS,2,2'-二硫二吡啶,Aldrithiol 2,Orthopyridyl disulfide |
Others | Others |
2,2′-Dipyridyl disulfide (Aldrithiol 2) 是肽化学中的常用试剂,是测定巯基的有用试剂,常用于氧化还原缩合以形成肽键或用于偶联反应以形成二硫键连接的异二聚体。 | |||
T3088 |
N-Ethylmaleimide
1-Ethyl-1H-pyrrole-2,5-dione,n-乙基马来酰亚胺,Ethylmaleimide,NEM |
Cysteine Protease; DUB | Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Proteases/Proteasome; Ubiquitination |
N-Ethylmaleimide (NEM) 是烷基化自由巯基的试剂, 是一种半胱氨酸蛋白酶抑制剂,用于实验生化研究。它也是一种去泛素化酶抑制剂,特异性抑制线粒体中的磷酸盐转运。 | |||
T20121 |
L-Albizziin
NSC-132089,L-beta-Ureidoalanine,L-Albizziine,Albizzine,NSC 132089,Albizziin,L-脲基丙氨酸 |
Glutaminase | Proteases/Proteasome |
L-Albizziin (L-beta-Ureidoalanine) 是一种巯基试剂,是一种谷氨酰胺酶抑制剂,可用于研究癌症。 | |||
T19955 |
Biotin-HPDP
Pyridyldisulfide-biotin,Pyridyldithiol-biotin |
Others | Others |
Biotin-HPDP (Pyridyldithiol-biotin) 是一种巯基反应性生物素化试剂。 | |||
T21334 |
Bucillamine
DE-019,Thiobutarit,Tiobutarit,布西拉明,SA96,DE 019,DE019 |
VEGFR; Antioxidant | Angiogenesis; oxidation-reduction; Tyrosine Kinase/Adaptors |
Bucillamine (DE019) 可防止高危器官移植中的缺血/再灌注损伤,抑制 VEGF 的产生。 Bucillamine 是一种具有抗风湿和抗血管生成特性的口服活性巯基供体和抗氧化剂。 Bucillamine 可用于脉络膜新生血管和类风湿性关节炎的研究。 | |||
T17389 |
AMAS
|
Others | Others |
AMAS 是一种不可裂解的异双功能交联剂,具有 NHS 酯和马来酰亚胺基团,可实现含胺和巯基分子的共价结合。 | |||
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。 | |||
T6741 |
SPDP
SPDP Crosslinker |
Others | Others |
SPDP 是一种短链交联剂,用于通过 NHS 酯和吡啶基二硫醇反应基团与半胱氨酸巯基形成可切割(可还原)的二硫键,实现胺与巯基的共轭。它是一种可降解的 ADC 连接剂,可用于合成抗体偶联药物。 | |||
T18728 |
Sulfo-SMCC sodium
|
Others | Others |
Sulfo-SMCC sodium 是一种异双功能、不可裂解的 ADC 交联剂,带有 N-羟基琥珀酰亚胺酯和马来酰亚胺基团,分别与伯胺和巯基反应。 | |||
T5030 |
Zofenopril calcium
SQ26991,佐芬普利钙,Zofenopril (calcium) |
RAAS; Reactive Oxygen Species | Endocrinology/Hormones; Immunology/Inflammation; Metabolism; NF-κB |
Zofenopril calcium (SQ26991) 是一种抗氧化剂和血管紧张素转化酶 (ACE) 抑制剂。 | |||
T1484L |
Perindopril erbumine
培哚普利叔丁胺,培哚普利叔丁胺盐,S9490-3,Perindopril tert-butylamine salt |
Apoptosis; RAAS; MRP | Apoptosis; Endocrinology/Hormones; Immunology/Inflammation |
Perindopril erbumine (S9490-3) 是一种长效血管紧张素转换酶抑制剂。 | |||
T0893 |
Tinidazole
替硝唑,CP12574 |
Antibacterial; Antibiotic | Microbiology/Virology |
Tinidazole (CP12574) 是一种对厌氧菌和原生动物具有选择性抗菌活性的 5-硝基咪唑,是一种具有口服活性的抗菌剂。 | |||
T1756 |
Ilaprazole sodium
IY-81149 sodium,艾普拉唑钠 |
Proton pump; TOPK | MAPK; Membrane transporter/Ion channel |
Ilaprazole sodium (IY-81149 sodium) 是一种具有口服活性质子泵抑制剂,以剂量依赖性方式不可逆地抑制 H+/K+-ATPase,在兔壁细胞制剂中的 IC50为 6 μM。它也是一种有效的 T 细胞起源蛋白激酶(TOPK)抑制剂,用于胃溃疡的研究。 | |||
T26065 |
Rev 5975
|
||
Rev 5975 is a non-sulfhydryl ACE-inhibitor. | |||
T70884 | Moexipril methyl ester | ||
Moexipril methyl ester is a long-acting, non-sulfhydryl angiotensine-converting enzyme inhibitor. | |||
T26067 |
Rev 6207
Rev-6207 |
||
Rev 6207 is a non-sulfhydryl ACE-inhibitor. | |||
T20758 |
Trandolaprilat
RU44403,RU-44403,Trandolaprilate,Trandolaprilatum,RU 44403 |
||
Trandolaprilat is an inhibitor of non-sulfhydryl angiotensin-converting enzyme. | |||
T26066 |
Rev 6134
Rev6134,Rev-6134 |
||
Rev 6134 is an ACE-inhibitor with non-sulfhydryl containing. | |||
T21269 |
Sulfo-EMCS
|
||
Sulfo-EMCS is a heterobifunctional sulfhydryl- and amine-reactive crosslinker. | |||
T19956 |
Iodoacetyl-LC-Biotin
Iaa-Biotin |
||
Iodoacetyl-LC-Biotin reacts with sulfhydryl groups to form stable thioether linkages. | |||
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 | |||
T71555 |
Moexipril ethyl ester
|
||
Moexipril ethyl ester is a long-acting, non-sulfhydryl angiotensine-converting enzyme inhibitor. | |||
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 | |||
T19437 |
MTSEA hydrobromide
|
Others | Others |
MTSEA hydrobromide is a sulfhydryl-reactive compound that modifies free cysteine residues to produce a positively charged side chain similar in size to lysine. | |||
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. | |||
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. | |||
T81904 |
Lucifer yellow iodoacetamide dipotassium
|
||
Lucifer yellow iodoacetamide dipotassium为一种反应性巯基荧光示踪剂,具备巯基与特定生物分子反应的能力,广泛应用于生物化学与分子生物学研究中。 | |||
T17834 |
DM4-SPDP
|
Others | Others |
DM4-SPDP, a drug-linker conjugate, integrates the antitubulin agent DM4 with the linker SMCC, facilitating the creation of antibody drug conjugates[1]. Additionally, SPDP serves as a short-chain crosslinker enabling amine-to-sulfhydryl conjugation, leveraging NHS-ester and pyridyldithiol groups to establish cleavable (reducible) disulfide bonds with cysteine sulfhydryls[2][3]. | |||
T27974 |
Maleimide-PEG4-NHS
MAL-PEG-NHS,Maleimide PEG NHS,Maleimido-Tetra(Ethylene Glycol)-Acetic Acid NHS ester,MAL-PEG4-NHS |
||
Maleimide-PEG4-NHS is a sulfhydryl and amine reactive heterofuncational PEG linker. The chemical bonds formed through Maleimide-PEG4-NHS linker are stable and are not cleavable. The NHS ester reacts with amino groups at pH 7-9 to form stable amide bond wh | |||
T71768 | CB10-277 | ||
CB10-277 is a synthetic derivative of dimethylphenyl-triazene related to dacarbazine, with antineoplastic properties. Related to the agent dacarbazine, CB10-277 is converted in vivo to a monomethyl triazene form that alkylates DNA, resulting in inhibition of DNA replication and repair; in addition, this agent may act as a purine analogue, resulting in inhibition of DNA synthesis, and may interact with protein sulfhydryl groups. | |||
T38351 |
DYn-2
|
||
Mild oxidation can convert the sulfhydryl group of cysteine residues on proteins to cysteine-sulfenic acid derivatives (Cys-SOH). Protein sulfenylation, then, is a post-translational modification that is relevant to redox signaling. DYn-2 is a chemoselective probe for detecting sulfenylated proteins in intact cells. DYn-2 consists of 1,3-cyclohexanedione coupled to an alkyne moiety by a 3-carbon spacer. The cyclohexanedione group selectively reacts with protein sulfenic acid modifications. The a... | |||
T68012 | rebimastat | ||
Rebimastat 是基于巯基的第二代基质金属蛋白酶(MMP)抑制剂,具有潜在的抗肿瘤活性。利莫司他选择性抑制几种 MMPs (MMP 1、2、8、9和14),从而诱导细胞外基质降解,抑制血管生成、肿瘤生长、侵袭和转移。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T1085L |
Glutathione oxidized
Bi(glutathion-S-yl),Oxidized glutathione,L-谷胱甘肽(氧化型),氧化型谷胱甘肽,L-Glutathione oxidized,Glutathione disulfide,L(-)-Glutathione,GSSG |
Reactive Oxygen Species; Endogenous Metabolite; Glutathione reductase | Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
Glutathione oxidized (L(-)-Glutathione) 是氧化型谷胱甘肽,谷胱甘肽是细胞内一种主要的抗氧化剂和解毒剂。 | |||
T1630 |
Tiopronin
Thiopronine,硫普罗宁,Acadione,Captimer |
ROS | Immunology/Inflammation |
Tiopronin (Acadione) 是可扩散的抗氧化剂,是重金属中毒的解毒剂和辐射防护剂。它可控制胱氨酸沉淀和排泄的速度,有用于胱氨酸尿症、类风湿性关节炎和肝病的研究潜力。 | |||
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. | |||
T75671 | Senecionine acetate | ||
Senecionine acetate (O-Acetylsenecionine)为吡咯烷核生物碱,通过使游离巯基失活,抑制线粒体及其区域内Ca2+的螯合。 | |||
T10928 |
Cytochalasin A
|
HIV Protease | Microbiology/Virology; Proteases/Proteasome |
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), inhibits actin polymerization and interferes with microtubule assembly by reacting with sulfhy |