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9
Cat. No. | Product Name | Target | Signaling Pathways |
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TP1869L |
Antioxidant peptide A acetate
Antioxidant peptide A acetate (159147-88-3 free base) |
Others | Others |
Antioxidant peptide A acetate (159147-88-3 free base) 是一种短肽,它含有替代的芳香族或含硫氨基酸。 | |||
T0352 |
Dibenzothiophene
二苯并噻吩,Imino semicarbazide,Diphenylene sulfide |
Others | Others |
Dibenzothiophene (Imino semicarbazide) 是有机合成过程的中间体,是由两个苯环稠合到一个中心的噻吩环。 | |||
T20290 |
Thianthrene
AI3 00638,AI300638,NSC-439,AI3-00638,噻蒽,dibenzo-1,4-dithiin,9,10-Dithiaanthracene,NSC439,Dibenzodithiodioxane,NSC 439 |
Others | Others |
Thianthrene (Dibenzodithiodioxane) 是一种含硫杂环化合物,是称为二硫因的母体杂环的衍生物,易于氧化。 | |||
T50009L |
sodium 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate
|
Others | Others |
sodium 3-amino-4,6-dimethylthieno[2,3-b]pyridine-2-carboxylate 是一种有机硫化合物。它已被用作研究含硫化合物对酶活性和代谢途径的影响的模型化合物,也被用于研究含硫化合物对细菌生长和基因表达调控的影响。 | |||
T24771 |
SCH-336
SCH336,SCH 336 |
Cannabinoid Receptor | GPCR/G Protein |
SCH-336是一种 CB2受体激动剂(Ki-1.8 nM, EC50-2 nM),具有有效性,选择性和口服活性。SCH-336对 CB1受体也具有生物活性,对CB2受体的选择性是CB1的100倍。SCH-336能够减少鸟苷5'-3- o -(硫)三磷酸与含hCB 的膜的结合,抑制 BaF3/CB2 细胞迁移,抑制小鼠延迟型超敏反应模型中的白细胞迁移,抑制小鼠过敏模型中抗原诱导的肺嗜酸性粒细胞增多。 | |||
T31760 |
Felinine
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Felinine is a sulfur-containing amino acid. | |||
TP1869 |
Antioxidant peptide A
|
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Antioxidant peptide A is a short peptide, which contains alternative aromatic or sulfur-containing amino acid. | |||
T19299 |
DTE
Cleland’s reagent,Dithioerythritol |
Others | Others |
Dithioerythritol (DTE), a sulfur-containing sugar derivative of the 4-carbon monosaccharide erythrose, is an epimer of dithiothreitol (DTT). | |||
T38437 |
NMTCA
N-Nitroso-2-methylthiazolidine4-carboxylicacid,NMTPRO,N-nitrosomethylthioproline |
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NMTCA (NMTPRO) is a sulfur-containing N-nitrosamino acid utilized as an endogenous nitrosation indicator in gas chromatography-thermal energy analysis. | |||
T36141 |
Boscalid
|
Mitochondrial Metabolism | Metabolism |
Boscalid 是一种广谱羧酰胺类杀菌剂,通过与线粒体复合物 II/琥珀酸脱氢酶的泛醌位点结合来抑制真菌呼吸。 | |||
T32655 |
l-Ergothionine hydrochloride
l-Ergothionine HCl |
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l-Ergothionine hydrochloride is a sulfur-containing amino acid, which is only produced by Actinomycetales bacteria and non-yeast-like fungi belonging to the division Basidiomycota and Ascomycota. It was originally isolated from Claviceps purpurea or rye e | |||
T68291 |
APSR-IN-8
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APSR-IN-8 is a first-in-class inhibitor of APS reductase (APSR), which is a critical enzyme in the assimilation of sulfate for the biosynthesis of cysteine and other essential sulfur-containing molecules. | |||
T75025 | ChoKα inhibitor-5 | ||
ChoKα inhibitor-5,一种含硫胆碱激酶(Choline Kinase)抑制剂,对HChoK α1表现出显著抑制效果,IC50值为0.64 μM。此外,该化合物还可诱导细胞凋亡,常用于癌症相关研究领域。 | |||
T75024 | ChoKα inhibitor-3 | ||
ChoKα inhibitor-3 是一种含硫的胆碱激酶抑制剂。ChoKα inhibitor-3 可抑制 HChoK α1,IC50值为 0.66 μM。ChoKα inhibitor-3 也可诱导凋亡。ChoKα inhibitor-3 可用于癌症的研究。 | |||
T83828 |
Sp-2'-Deoxycytidine-5'-O-(1-thiotriphosphate) sodium
Sp-dCTP-α-S |
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Sp-2'-Deoxycytidine-5'-O-(1-thiotriphosphate) (Sp-dCTP-α-S) 是含硫核苷酸衍生物 dCTP-α-S 的异构体。它抑制解氧核苷酸三磷酸三磷酸水解酶 SAMHD1(Ki = 6.3 µM)。 | |||
T83831 |
Sp-2'-Deoxyguanosine-5'-O-(1-thiotriphosphate) sodium
Sp-dGTP-α-S |
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Sp-2'-Deoxyguanosine-5'-O-(1-thiotriphosphate) 是一种含硫异构体,属于核苷酸三磷酸2'-脱氧鸟苷-5'-O-三磷酸(dGTP)。它通过抑制脱氧核苷酸三磷酸三磷酸水解酶SAMHD1 (Ki = 820 nM)发挥作用。 | |||
T83834 |
Sp-Guanosine-5'-O-(1-thiotriphosphate) sodium
Sp-GTP-α-S,GTPαS(Sp),GTPαS(A) |
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Sp-Guanosine-5'-O-(1-thiotriphosphate) (Sp-GTP-α-S) 是一种含硫核苷酸衍生物GTP-α-S的异构体。它能结合到微管蛋白上,在20 mM的浓度下用于无细胞实验时可诱导微管组装。 | |||
T83837 |
Rp-Thymidine-5'-O-(1-thiotriphosphate) sodium
Rp-dTTP-α-S |
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Rp-Thymidine-5'-O-(1-thiotriphosphate) (Rp-TTP-α-S) 是含硫核苷酸衍生物 TTP-α-S 的一个异构体。它能与HIV-1逆转录酶结合(在镁、锰酸盐和钴存在下的Kds分别为45.7、27.32和39.44 µM)。 | |||
T83833 |
Rp-2'-Deoxyuridine-5'-O-(1-thiotriphosphate) sodium
Rp-dUTP-α-S |
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Rp-2'-Deoxyuridine-5'-O-(1-thiotriphosphate) (Rp-dUTP-α-S) 是含硫核苷酸 dUTP-α-S 的同分异构体,也是嘌呤P2Y2受体的激动剂。在表达P2Y2受体的1321N1星形胶质瘤细胞中,该化合物特异性诱导肌醇磷酸积累(EC50 = 12.5 µM),相较于表达P2Y4的1321N1细胞,在10 µM浓度下效果更显著。 | |||
T83838 |
Sp-Thymidine-5'-O-(1-thiotriphosphate) sodium
Sp-TTP-α-S |
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Sp-Thymidine-5'-O-(1-thiotriphosphate)(Sp-TTP-α-S)是含硫核苷酸衍生物TTP-α-S的一个异构体。它能够结合HIV-1逆转录酶(在镁、锰酸盐和钴存在时,Kds分别为2.88、4.23和20.21 µM)。Sp-TTP-α-S抑制脱氧核苷酸三磷酸三磷酸水解酶SAMHD1(Ki为46 nM)。 | |||
T37362 |
7α-Thiomethylspironolactone
|
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7α-Thiomethylspironolactone is a major metabolite of the synthetic steroid spironolactone.1,2 1.Jankowski, A., Skorek-Jankowska, A., and Lamparczyk, H.Simultaneous determination of spironolactone and its metabolites in human plasmaJ. Pharm. Biomed. Anal.14(8-10)1359-1365(1996) 2.Gardiner, P., Schrode, K., Quinlan, D., et al.Spironolactone metabolism: Steady-state serum levels of the sulfur-containing metabolitesJ. Clin. Pharmacol.29(4)342-347(1989) | |||
T83805 |
Rp-Adenosine-5'-O-(1-thiodiphosphate) sodium
Rp-ADP-α-S |
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Rp-Adenosine-5'-O-(1-thiodiphosphate)(Rp-ADP-α-S)是ADP-α-S的含硫异构体,是磷酸化酶激酶的抑制剂(Ki = 0.53 µM)。此化合物能诱导分离的人类血小板聚集(EC50 = 20 µM),并能引发经卡巴胆碱预收缩的豚鼠乙状结肠松弛(EC50 = 58.9 µM)。 | |||
T83806 |
Sp-Adenosine-5'-O-(1-thiodiphosphate) sodium
Sp-ADP-α-S |
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Sp-Adenosine-5’-O-(1-thiodiphosphate) (Sp-ADP-α-S) 是硫含量核苷酸衍生物ADP-α-S的一种异构体。它是磷酸化酶激酶的抑制剂(Ki = 0.53 µM)。Sp-ADP-α-S能引起人类孤立血小板聚集(EC50 = 20 µM),并能使羧胺胆碱预收缩的豚鼠taenia coli松弛(EC50 = 58.9 µM)。 | |||
T83808 |
Sp-Adenosine-5'-O-(1-thiotriphosphate) sodium
Sp-ATP-α-S |
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Sp-Adenosine-5'-O-(1-thiotriphosphate) (Sp-ATP-α-S) 是一种含硫核苷酸衍生物 ATP-α-S 的异构体,也是嘌呤P2Y1受体的激动剂。在表达P2Y1受体的HEK293细胞中增加钙离子的流动(对人类受体的EC50 = 9.4 nM)。Sp-ATP-α-S 抑制了ADP诱导的孤立人类血小板聚集(Ki = 4 μM)。它还能引起经卡巴胆碱预收缩的豚鼠十二指肠松弛(EC50 = 426 nM)。 | |||
T83807 |
Rp-Adenosine-5'-O-(1-thiotriphosphate) sodium
Rp-ATP-α-S |
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Rp-Adenosine-5'-O-(1-thiotriphosphate)(Rp-ATP-α-S)是一种含硫核苷酸衍生物ATP-α-S的异构体,同时也是嘌呤P2Y1受体的激动剂。在表达人类P2Y1受体的HEK293细胞中,Rp-ATP-α-S能增加钙的动员(EC50 = 75 nM)。该化合物与洗涤的人类孤立血小板结合(Ki = 156 nM),抑制由ADP引发的人类富血小板血浆(PRP)的聚集(pA2 = 4.74),并且能够抑制前列腺素E1(PGE1)在人类孤立PRP中引发的cAMP产生(pA2 = 5.26)。同时,Rp-ATP-α-S还能引起用氨基甲酰胆碱预先缩紧的豚鼠结肠条带的松弛(EC50 = 56 nM)。此外,Rp-ATP-α-S已经被用于合成被细菌核糖开关识别的环状二核苷酸。 |
Cat. No. | Product Name | Target | Signaling Pathways |
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T39668 |
Methyl propyl disulfide
|
Others | Others |
Methyl propyl disulfide 是在大蒜和洋葱中产生的挥发性含硫化合物,具有抗癌活性。 | |||
T19081 |
1,3-Dithiane
1,3-Dithian,M-DITHIANE,1,3-Dithiacyclohexane,1,3-二噻烷 |
Anti-infection; Endogenous Metabolite; Antibacterial | Metabolism; Microbiology/Virology |
1,3-Dithiane (1,3-Dithian) 是一种受保护的甲醛阴离子等价物,可用作有用的标记合成子。它是在煮熟的牛肉提取物中发现的含硫美拉德反应产物 。 | |||
T60789 |
L-Cystine dihydrochloride
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L-Cystine dihydrochloride 是合成谷胱甘肽 (GSH) 的含硫前体。L-Cystine dihydrochloride 的稳态对谷胱甘肽的功能很重要。L-Cystine dihydrochloride 可用作细胞培养组分。 | |||
T10939L |
L-Cystathionine
L-胱硫醚,Cystathionine,ZINC1532680,L-(+)-Cystathionine,Cystathionine, L- |
Apoptosis; Endogenous Metabolite | Apoptosis; Metabolism |
L-Cystathionine (Cystathionine, L-) 是一种与含硫氨基酸的代谢条件有关的关键非蛋白质氨基酸。L-Cystathionine 可用于有关心血管保护的研究。 | |||
T22311 |
Djenkolic Acid
jengkolic acid,Djenkolate,3,3'-(亞甲二硫)雙丙胺酸,S,S'-Methylenebiscysteine |
Others | Others |
Djenkolic Acid (S,S'-Methylenebiscysteine) 是天然存在于东南亚植物 Archidendron jiringa 的 Djenkol 豆中的含硫非蛋白质氨基酸。它是人类急性肾损伤的一个不常见但重要的原因。 | |||
T2O2733 |
L-Cystine
Cystine Acid,cystine,胱氨酸,L-胱氨酸 |
Antioxidant; Ferroptosis; Endogenous Metabolite | Apoptosis; Metabolism; oxidation-reduction |
L-Cystine (Cystine Acid) 是一种从半胱氨酸氨基酸硫醇侧链氧化获得的含硫衍生物。它起到抗氧化剂的作用,保护组织免受辐射和污染,减缓衰老过程。它还有助于蛋白质合成。 | |||
T2O2721 |
L-Cysteine
Thioserine,L-半胱氨酸,cysteine,半胱氨酸,L-(+)-Cysteine |
Endogenous Metabolite | Metabolism |
L-Cysteine (L-(+)-Cysteine) 是人体非必需的含硫氨基酸。L-Cysteine 对蛋白质合成、解毒和多种代谢功能很重要。L-Cysteine 存在于指甲、皮肤和头发的主要蛋白质-角蛋白中,对胶原蛋白的生成、皮肤弹性和质地都很重要。L-Cysteine 是抗氧化剂谷胱甘肽的一种成分,在辅酶A、肝素和生物素等基本生化物质的代谢中起着重要作用,也是氨基酸牛磺酸的制造所必需的。 | |||
T17173 |
Tropodithietic acid
|
Others | Others |
Tropodithietic acid, a sulfur-containing antibiotic produced by the marine bacterium Phaeobacter inhibens, exhibits potent antibiotic efficacy across a diverse array of bacteria, encompassing alpha- and gammaproteobacteria, flavobacteria, and actinobacteria. | |||
T35624 | Ajoene | ||
Ajoene is a disulfide that has been found inA. sativumand has diverse biological activities, including antibacterial, anticancer, antiplatelet, and antioxidant properties.1,2,3,4It is active against Gram-positive (MICs = 5-160 µg/ml) and Gram-negative bacteria (MICs = 136-200 µg/ml), as well as yeasts (MICs = 10-20 µg/ml).1Ajoene is cytotoxic to mouse melanoma cells (IC50= 18 µM), as well as human colon, lung, mammary, and pancreatic cancer cells (IC50s = 7-41 µM).2It reduces... |