130
6
Cat. No. | Product Name | Target | Signaling Pathways |
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T11372 |
GC7 Sulfate
|
Autophagy | Autophagy |
GC7 Sulfate 是 deoxyhypusine synthase(DHS)有效抑制剂。真核翻译起始因子5A2 (eIF5A2)是DHS 已知的底物,因此GC7通过抑制DHS 活性来抑制eIF5A2的激活。 | |||
T5188 |
GC376 sodium
|
SARS-CoV | Microbiology/Virology |
GC376 sodium 是一种 3C 样蛋白酶 (3CLpro) 抑制剂,IC50 值范围为 0.49~4.35 μM。 | |||
T24086 |
GC 10284
GC10284,GC-10284 |
||
GC 10284 is an agent of pesticide. | |||
T76681 |
Fresolimumab
GC1008 |
TGF-beta/Smad | Stem Cells |
Fresolimumab (GC1008) 是一种具有特异性的人抗转化生长因子 β单克隆抗体,可与人 TGFβ1、TGFβ2 和 TGFβ3 的活性形式结合,可用于研究成人局灶节段性肾小球硬化和癌症。 | |||
T11376 | GC 14 | Others | Others |
GC 14 is a selective thyroid hormone receptor antagonist, with IC50 values of 200 nM and 35 nM for hTRα and hTRβ, respectively. | |||
T71877 |
GC-204
|
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GC-204 is a selective inhibitor of carbonic anhydrase ix (caix) | |||
T69734 |
Org GC 94
|
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Org GC 94 is a serotonin antagonist; anti-migraine. | |||
T5313 |
Sobetirome
IACS-010759,QRX-431 |
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
Sobetirome (IACS-010759) 是一种甲状腺激素受体 β (TRβ) 激动剂,能够选择性的结合到TRβ-1(EC50:0.16 μM)。 | |||
T9080 |
Plecanatide
|
Guanylate cyclase | GPCR/G Protein |
Plecanatide 是尿鸟苷蛋白的类似物,是一种可口服的鸟苷酸环化酶-C (GC-C) 受体激动剂。在 T84 细胞实验中,它激活 GC-C 受体以刺激 cGMP 合成的EC50值为 190 nM。在小鼠结肠炎模型中,它具有抗炎活性。 | |||
T40548 |
NH-3
|
Thyroid hormone receptor(THR) | Endocrinology/Hormones |
NH-3是一种高效的口服活性甲状腺激素受体(THR)拮抗剂,具有可逆行为,其IC 50为55 nM。NH-3源自选择性甲状腺激素模拟物GC-1,有效地抑制甲状腺激素与相应受体的结合,从而阻碍辅因子的招募。 | |||
T29251 |
(±)-GC242
GC242,(±) GC242 |
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(±)-GC242 is a profluorescent RAMOSUS3 (RMS3) probe with strigalactone-like biological activity. | |||
T69840 |
MX106
|
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MX106 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation. | |||
T30959 |
CK-119
CK 119,GC-6119,UNII-AL53N923EI |
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CK-119 is an interleukin-1 blocker, which mainly inhibits the growth of fibroblast-like corneal and conjunctival cells by inhibiting the synthesis of DNA and RNA. | |||
T39763 |
Rucosopasem manganese
GC4711 |
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Rucosopasem manganese (GC4711) is a potent, selective superoxide dismutase (SOD) mimetic capable of efficiently converting superoxide to hydrogen peroxide. This compound, specifically designed for research purposes, holds promise in cancer-related studies. | |||
T69733 |
LM9
|
||
LM9 is a MyD88 inhibitor which prevents atherosclerosis by regulating inflammatory responses and oxidative stress in macrophages. | |||
T69841 | GC813 sodium | ||
GC813 is a potent and permeable inhibitor of MERS coronavirus 3CL protease. GC813 is analogue of GC376. | |||
T40544 |
NCGC00092410
ML008 |
Glucosidase | Metabolism |
NCGC00092410 (ML008) 是一种葡萄糖脑苷脂酶 (glucocerebrosidase, GC) 抑制剂,IC50 值为 31 nM。可用于由糖脑苷酶基因突变引起的戈谢病的研究。 | |||
TP1267L |
CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate
CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate(254110-79-7 free base) |
Others | Others |
CEF27, Epstein-Barr Virus BRLF-1 lytic 148-156 acetate(254110-79-7 free base) 对应于 BRLF1 的氨基酸 148-156。 BRLF1 是一种转录激活因子,可直接与一些 Epstein-Barr 病毒 (EBV) 裂解基因启动子中的富含 GC 的基序结合。 | |||
T16947 |
SU16f
3-substituted indolin-2-one 16f,SU-16F,SU 16F |
PDGFR | Angiogenesis; Tyrosine Kinase/Adaptors |
SU16f (3-substituted indolin-2-one 16f) 是一种有效的,选择性 PDGFRβ 抑制剂,对 PDGFRβ,PDGFR1,PDGFR2 的 IC50 分别为 10 nM,140 nM,2.29 μM。SU16f 抑制 PDGFRβ 受体从而可以阻断胃癌来源的间充质干细胞 (GC-MSC) 条件培养基在胃癌细胞增殖和迁移中的促进作用。 | |||
T12670 |
(Rac)-MGV354
MGV354,外消旋MGV354 |
Others | Others |
(Rac)-MGV354 (MGV354) 是 MGV354 的外消旋体,MGV354 是可溶性鸟苷酸环化酶活化剂,在 GTM-3E 和 CHO 细胞中 EC50分别为 5 nM 和小于 0.5 nM。 | |||
T6888 |
Methylene Blue
亚甲蓝,methylthioninium chloride,CI-52015,Tetramethylthionine chloride,亚甲兰,Basic Blue 9 |
Guanylate cyclase; Microtubule Associated; NO Synthase; Parasite; Monoamine Oxidase | Cytoskeletal Signaling; GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Methylene Blue (Tetramethylthionine chloride) 是鸟苷酸环化酶,是单胺氧化酶 A 和 NO 合酶抑制剂。它有抗伤害感受、抗疟疾、抗抑郁和抗焦虑作用,可研究高铁血红蛋白血症、神经退行性疾病和异环磷酰胺引起的脑病。它是血管加压剂,用作色素内窥镜检查中的染料。 | |||
T2090 |
Lexibulin
CYT-997 |
Apoptosis; Reactive Oxygen Species; Microtubule Associated | Apoptosis; Cytoskeletal Signaling; Immunology/Inflammation; Metabolism; NF-κB |
Lexibulin (CYT-997) 是一种微管蛋白聚集强效抑制剂,可诱导细胞凋亡,并诱导 GC 细胞中的线粒体ROS 生成。它对多种癌细胞的 IC50 值为 10-100n M,在体内外具有高细胞毒性和血管增生阻断作用。 | |||
T12501 |
Plecanatide acetate
|
Others | Others |
Plecanatide acetate is a agonist of guanylate cyclase-C (GC-C) receptor( EC50 of 190 nM in T84 cells), and shows anti-inflammatory activity in models of murine colitis. | |||
T11422 | Glutaminyl Cyclase Inhibitor 3 | Others | Others |
Glutaminyl Cyclase Inhibitor 3, a designed anti-Alzheimer’s compound, is a potent human Glutaminyl Cyclase (GC) inhibitor (IC50: 4.5 nM). It significantly reduced the brain concentrations of pyroform Aβ and total Aβ and restored cognitive functions. | |||
T68877 |
Tetrahydrocorticosterone
|
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Tetrahydrocorticosterone (THB) is a glucocorticoid (GC) that has anti-inflammatory functions. For instance, 5α THB inhibits inflammatory actions by binding to GC receptor. HPLC studies in rat brains have reported that tetrahydrocorticosterone (THB) isomers are differentially distributed in males and females. | |||
T78573 |
Glucocerebrosidase
GCase,Glucosylceramidase |
Endogenous Metabolite | Metabolism |
Glucocerebrosidase (Glucosylceramidase; GBA) 是溶酶体内的酶,负责催化GC中的β-糖苷键裂解,从而生成葡萄糖和神经酰胺。 | |||
T10535L | BI 653048 phosphate | P450 | Metabolism |
BI 653048 phosphate is a selective and orally active agonist of nonsteroidal glucocorticoid (GC)(IC50 : 55 nM). | |||
T22615 |
BPIPP
|
Others | Others |
guanylyl cyclase (GC) and adenylyl cyclase (AC) inhibitor | |||
T76274 |
Dolcanatide
|
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Dolcanatide为一种对GC-C(鸟苷酸环化酶-C)具有口服活性的激动剂,展现出通便、抗痛及抗炎效果,适用于炎症性肠病研究。 | |||
T73940 |
S-Phenylmercapturic acid
|
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S-Phenylmercapturic acid,苯的代谢物,作为生物标志物使用,可通过GC、HPLC(UV或荧光检测)、GC-MS、LC-MS/MS或免疫测定进行检测。 | |||
T83247 | 7-Deaza-dGTP tetralithium | ||
7-Deaza-dGTP tetralithium可用于高效扩增富含GC序列的DNA。 | |||
T37031 |
Quinacrine mustard hydrochloride
Quinacrine mustard HCl |
Autophagy | Autophagy |
Quinacrine mustard hydrochloride 是一种荧光染料,也 是一种多环芳香剂,可作为诱变剂诱导细菌的突变体。Quinacrine mustard hydrochloride 能选择性地与腺嘌呤-胸腺嘧啶(AT)碱基对结合,而不 是与鸟嘌呤-胞嘧啶(GC)碱基对结合,诱导细胞周期停滞在 G2/M 期。Quinacrine mustard (hydrochloride) 已被用于标记移相染色体,以通过自动放射摄影技术进行核型分析。 | |||
T37365 |
7-hydroxy Coumarin sulfate (potassium salt)
|
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7-hydroxy Coumarin sulfate is a phase II metabolite of coumarin that can be used as an internal standard for the analysis of 7-hydroxy coumarin metabolism using GC- or LC-MS. | |||
T37438 |
C17 Globotriaosylceramide (d18:1/17:0)
C17 Globotriaosylceramide (d18:1/17:0) |
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C17 Globotriaosylceramide is a sphingolipid that has been used as an internal standard for the quantification of globotriaosylceramides in plasma and urine from patients with Fabry disease by GC-MS. | |||
T35515 |
3-Acetyldeoxy Nivalenol-13C17
3-Acetyldeoxy Nivalenol-13C17 |
||
3-Acetyldeoxy nivalenol-13C17is intended for use as an internal standard for the quantification of 3-acetyldeoxy nivalenol by GC- or LC-MS. 3-Acetyldeoxy nivalenol is a mycotoxin that has been found inF. graminearum.1In vivo, 3-acetyldeoxy nivalenol (40 mg/kg) induces duodenal and splenic cell necrosis, as well as lethality (LD50= 70 mg/kg) in mice.2 1.Jiao, F., Kawakami, A., and Nakajima, T.Effects of different carbon sources on trichothecene production and Tri gene expression by Fusarium grami... | |||
T37258 |
13-methyl Myristic Acid methyl ester
|
||
13-methyl Myristic acid methyl ester is a methylated bacterial fatty acid methyl ester. It has been used as a marker of bacteria in sewage sludges and of bacterial contaminants in pharmaceutical manufacturing by GC-MS. | |||
T38037 |
Caffeic Acid-13C3
Caffeic Acid-13C3 |
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Caffeic acid-13C3 is an isotopically enriched form of caffeic acid that is intended for use as an internal standard for the quantification of caffeic acid by GC- or LC-MS. Caffeic acid is an inhibitor of 5-LO , with IC50 values of 3.7-72 μM, and 12-LO, with IC50 values of 5.1-30 μM. | |||
T70893 | K811 | ||
K811 is an ASK1-specific inhibitor that prolongs survival in a mouse model of amyotrophic lateral sclerosis. K811 efficiently prevented cell proliferation in cell lines with high ASK1 expression and in HER2-overexpressing GC cells. Treatment with K811 reduced sizes of xenograft tumors by downregulating proliferation markers. | |||
T35697 |
Lauric Acid-13C
|
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Lauric acid-13C is intended for use as an internal standard for the quantification of lauric acid by GC- or LC-MS. Lauric acid is a medium-chain saturated fatty acid. It has been found at high levels in coconut oil.1Lauric acid induces the activation of NF-κB and the expression of COX-2, inducible nitric oxide synthase (iNOS), and IL-1α in RAW 264.7 cells when used at a concentration of 25 μM.2 | |||
T71500 |
Palifosfamide tromethamine
IPM tromethamine,Isophosphoramide mustard tromethamine,ZIO-201 tromethamine,Isophosphoramide mustard tromethamine ; IPM tromethamine ; ZIO-201 tromethamine |
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Palifosfamide (tromethamine) 是一种具有潜在抗肿瘤活性的合成烷基化剂。作为异环磷酰胺 (ifosfamide) 稳定的活性代谢物,Palifosfamide (tromethamine) 通过GC 碱基对不可逆地烷基化和交联DNA,导致了DNA 复制的抑制,并导致细胞死亡。与异环磷酰胺相比,Palifosfamide (tromethamine)的毒性较小。 | |||
T35462 | (±)11-HETE | ||
(±)11-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid . The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC. The racemic HETEs have been quantified as an index of lipid peroxidation using GC/MS. | |||
T36383 |
L-Thyroxine-13C9,15N
L-Thyroxine-13C9,15N |
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L-Thyroxine-13C9,15N is intended for use as an internal standard for the quantification of L-thyroxine by GC- or LC-MS. L-Thyroxine is a synthetic form of the thyroid hormone thyroxine. In vivo, L-thyroxine (0.9 and 2.7 μg) inhibits synthesis and release of thyrotropin induced by thyrotropin-releasing hormone from the anterior pituitary in mice. It also reverses decreases in levels of circulating thymic serum factor (FTS) and the number of T rosette-forming cells in an old age-induced mouse mode... | |||
T36558 |
(±)9-HETE
|
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(±)9-HETE is one of the six monohydroxy fatty acids produced by the non-enzymatic oxidation of arachidonic acid. The individual R and S isomers of racemic HETEs have been separated and identified using chiral phase HPLC. The racemic HETEs have been quantified as an index of lipid peroxidation using GC/MS. | |||
T71893 |
Clobetasol Propionate-d5
|
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Clobetasol propionate-d5 is intended for use as an internal standard for the quantification of clobetasol propionate by GC- or LC-MS. Clobetasol propionate is a corticosteroid. It binds to glucocorticoid receptors in a cell-free assay and inhibits proliferation of primary human skin fibroblasts when used at a concentration of 5 µg/ml. Topical administration of clobetasol propionate reduces croton oil-induced ear edema in mice. Formulations containing clobetasol propionate have been used in the t... | |||
T78165 | SPEN inhibitor 1 | Others | Others |
SPEN-IN-1(compound X1)是一种针对蛋白因子SPEN的抑制剂,其Kd值达47 nM。该化合物对于RepA显示出高度的选择性,RepA为Xist(非编码RNA原型)中包含431个核苷酸的结构域,由8.5个GC-rich基序构成,这些基序参与基因的沉默作用。 | |||
T35513 |
13C15-Nivalenol
13C15-Nivalenol |
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13C15-Nivalenol is intended for use as an internal standard for the quantification of nivalenol by GC- or LC-MS. Nivalenol is a trichothecene mycotoxin that has been found inFusarium.1It is lethal to mice (LD50= 6.9 mg/kg).2Nivalenol (5, 10, and 15 mg/kg) also induces thymic, splenic, and Peyer's patch cell apoptosis in mice.3 1.Yang, Z., Concannon, J., Ng, K.S., et al.Tetrandrine identified in a small molecule screen to activate mesenchymal stem cells for enhanced immunomodulationSci. Rep.63026... | |||
T70035 |
Tasimelteon-d5
|
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Tasimelteon-d5 is intended for use as an internal standard for the quantification of tasimelteon by GC- or LC-MS. Tasimelteon is a melatonin (MT) receptor agonist. It selectively binds MT1 and MT2 receptors over a panel of 160 additional receptors and enzymes at 10 µM. Tasimelteon inhibits forskolin-induced cAMP accumulation with EC50 values of 0.79 and 1 nM in NIH3T3 cells expressing the MT1 or MT2 receptor, respectively. Formulations containing tasimelteon have been used in the treatment of no... | |||
T35521 |
Aflatoxin G2-13C17
Aflatoxin G2-13C17 |
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Aflatoxin G2-13C17is intended for use as an internal standard for the quantification of aflatoxin G2by GC- or LC-MS. Aflatoxin G2is a mycotoxin that has been found inAspergillus.1It is lethal to ducklings (LD50= 2.83 mg/kg) but is non-toxic to rats when administered at a dose of 200 mg/kg.2 1.Bennett, J.W., and Klich, M.MycotoxinsClin. Microbiol. Rev.16(3)497-516(2003) 2.Wogan, G.N., Edwards, G.S., and Newberne, P.M.Structure-activity relationships in toxicity and carcinogenicity of aflatoxins a... | |||
T36537 |
Nitrofurantoin-13C3
Nitrofurantoin-13C3 |
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Nitrofurantoin-13C3is intended for use as an internal standard for the quantification of nitrofurantoin by GC- or LC-MS. Nitrofurantoin is a nitrofuran antibiotic.1In vivo, nitrofurantoin (25-100 mg/kg) reducesE. colireplication and abscess formation in the renal medulla of infected rats in a dose-dependent manner. It prevents kidney and bladder infection in rats following bladder inoculation with clinical isolates ofP. mirabilis. Nitrofurantoin also prevents alkalization of urine, as well as ca... | |||
T36895 |
5-Fluorouracil-13C,15N2
5-Fluorouracil-13C,15N2 |
||
5-Fluorouracil-13C,15N2 is intended for use as an internal standard for the quantification of 5-flurouracil by GC- or LC-MS. 5-Fluorouracil is a pyrimidine analog that irreversibly inhibits thymidylate synthase, blocking the synthesis of thymidine which is required for DNA synthesis. Intracellular metabolites of 5-fluorouracil exert cytotoxic effects by either inhibiting thymidylate synthetase, or through incorporation into RNA and DNA, ultimately initiating apoptosis. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3828 |
(-)-Gallocatechin
(2S,3R)-gallocatechin,(−)-GC,(-)-棓儿茶酸;没食子儿茶素,没食子儿茶素 |
Others | Others |
(-)-Gallocatechin ((−)-GC) 是一种 (-)-Epigallocatechin (EGC) 的差向异构体,常存在于各种茶产品中,具有抗氧化特性。 | |||
TN6906 |
1-Pentadecene [Standard Material for GC]
|
||
1-Pentadecene [Standard Material for GC] is a natural product. | |||
T35618 |
D-Fructose-13C6
D-果糖 13C6 |
Others | Others |
D-Fructose-13C6 可用作通过 GC-或 LC-MS 定量 D-果糖的内标。 | |||
T5217 |
2-(2-Phenylacetamido)acetic acid
Phenaceturic acid,Phenyl-ac-Gly-OH,苯乙酰甘氨酸,Phenylacetyl glycine |
Others; Endogenous Metabolite | Metabolism; Others |
2-(2-Phenylacetamido)acetic acid (Phenyl-ac-Gly-OH) 是内源性代谢产物的一种。 | |||
T0019 |
Betaine chloride
Betaine hydrochloride,盐酸甜菜碱 |
Others; Chloride channel; Endogenous Metabolite | Membrane transporter/Ion channel; Metabolism; Others |
Betaine chloride (Betaine hydrochloride) 是一种天然化合物,在许多食物中能够发现,也是能够维持正常 DNA 甲基化模式的特性甲基供体。 | |||
TN6962 |
Docosane
|
Others | Others |
Docosane 是一种直链烷烃,可用于合成具有热能储存/释放能力的结构复合材料。 |