31
4
Cat. No. | Product Name | Target | Signaling Pathways |
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T31162 |
Cysteinyltyrosine
N-L-Cysteinyl-L-tyrosine,Cys-tyr |
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Cysteinyltyrosine is a dipeptide composed of cysteine and tyrosine. It is an incomplete breakdown product of protein digestion or protein catabolism. | |||
T8844 |
Diflapolin
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Others; FLAP; Epoxide Hydrolase | Immunology/Inflammation; Metabolism; Others |
Diflapolin 是高活性的双 5-脂氧合酶激活蛋白(FLAP)/可溶性环氧化物水解酶抑制剂,具有显著的抗炎作用和较高的靶向选择性。它抑制分离的 sEH 的活性,IC50为20 nM。它还抑制完整人单核细胞和中性粒细胞中 5-LOX 产物的形成,IC50分别为 30 和 170 nM。 | |||
T1677L |
Montelukast sodium
MK0476,孟鲁司特钠 |
Leukotriene Receptor; LTR | GPCR/G Protein; Immunology/Inflammation |
Montelukast sodium (MK0476) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 | |||
T1677 |
Montelukast
孟鲁司特,Singular |
Leukotriene Receptor; Lipoxygenase; LTR | GPCR/G Protein; Immunology/Inflammation; Metabolism |
Montelukast (Singular) 是可口服的半胱氨酸白三烯受体1 选择性拮抗剂,可用于研究预防哮喘和肝损伤。它还可减少心脏损伤,在肠缺血-再灌注损伤中也具有抗氧化作用。 | |||
T4233L |
Cysteinylglycine acetate
Cys-Gly Acetate,Cysteinylglycine acetate(19246-18-5 Free base) |
Endogenous Metabolite | Metabolism |
Cysteinylglycine acetate (Cys-Gly Acetate) 是Cysteinylglycine 的醋酸盐形式。Cysteinylglycine 是一种内源性代谢产物,可用于疾病诊断。 | |||
T32099 |
Homocysteinylpropachlor
Homo-cys-ipa |
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Homocysteinylpropachlor is a bioactive chemical. | |||
T15036 |
Cysteinylglycine TFA
|
Others | Others |
Cysteinylglycine TFA is an endogenous metabolite. It is used in disease diagnosis. | |||
T38206 |
3-Cysteinylacetaminophen (trifluoroacetate salt)
APAP-Cys,3-(cysteine-S-yl)acetaminophen,3-Cysteinylacetaminophen (trifluoroacetate salt) |
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3-Cysteinylacetaminophen is an acetaminophen-protein adduct formed during the metabolism of acetaminophen.[1],[2] 3-Cysteinylacetaminophen has been found in isolated human serum following therapeutic and supratherapeutic doses of acetaminophen and in the presence and absence of hepatotoxicity.[3],[4] In mice, 3-cysteinylacetaminophen decreases renal glutathione (GSH) levels, an effect that can be blocked by the γ-glutamyl inhibitor acivicin. | |||
T31161 |
Cysteinyllysine
|
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Cysteinyllysine is a dipeptide composed of cysteine and lysine. It is an incomplete breakdown product of protein digestion or protein catabolism. | |||
T31160 |
Cysteinylcysteine
Cys-cys |
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Cysteinylcysteine is a bioactive chemical. | |||
T19699 |
Triciribine phosphate
TCN-P,VD 002,VQD-002 |
Apoptosis; Akt | Apoptosis; Cytoskeletal Signaling; PI3K/Akt/mTOR signaling |
Triciribine phosphate (VD 002) 是一种高选择性的 AKT 抑制剂,可诱导细胞周期停滞和半胱天冬酶依赖性细胞凋亡,抑制新生血管的生成,可用于研究白血病。 | |||
T36333 |
Z-IETD-AFC
|
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Z-IETD-AFC 是 caspase-8 和颗粒酶 B 的荧光底物,可用于定量半胱天冬酶-8 或颗粒酶 B 的活性。 | |||
T0694 |
Pranlukast
普鲁司特,ONO-1078,普仑司特 |
Leukotriene Receptor; IL Receptor; Others; TNF; NF-κB; LTR | Apoptosis; GPCR/G Protein; Immunology/Inflammation; NF-κB; Others |
Pranlukast (ONO-1078) 是一种半胱氨酰白三烯受体 1 拮抗剂,可拮抗或减少支气管痉挛,用于哮喘研究。 | |||
T68130 |
Pobilukast
SKF 104353 Z2,SKF 104353 |
Leukotriene Receptor | GPCR/G Protein |
Pobilukast (SKF 104353) 是一种选择性半胱氨酰白三烯受体拮抗剂,可阻断磷脂酰肌醇代谢和白三烯D诱导的血栓素合成,可用于研究过度心肌再灌注损伤 (MI/R) 大鼠限制心肌损伤。 | |||
T11388 |
Gemilukast
ONO-6950 |
Others | Others |
Gemilukast(ONO-6950) 是一种具有口服活性和有效性的半胱氨酰白三烯 1 和 2 受体 (CysLT1 和CysLT2) 双重抑制剂,抑制 LTC 4 诱导的支气管收缩,对人 CysLT1 和 CysLT2 有抑制作用,可用于治疗哮喘。 | |||
T27912 |
LY 290324
LY-290324,LY290324 |
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LY 290324 is an orally active, potent and selective antagonist of cysteinyl leukotriene (LTD4) receptor. | |||
T31080 |
CP-85958
(+)-Cp 85958,UNII-CU98Q2IL7P |
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CP-85958 is a cysteinyl leukotriene antagonist. | |||
T28481 |
Q8 hydrochloride
Q8 |
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Q8 is an antagonist of cysteinyl leukotreine receptor. Q8 inhibits VEGF-independent angiogenesis. | |||
T37016 |
Iralukast (CGP 45715A)
|
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Iralukast is a cysteinyl-leukotriene antagonist (CysLT) with a pKi of 7.8 for CysLT1. | |||
T38129 |
Leukotriene F4
LTF4 |
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LTF4 is a cysteinyl-leukotriene produced in vitro, but not reported to date in vivo. It is formed by the incubation of LTE4 with γ-glutamyl transpeptidase and glutathione. LTF4 is a weak agonist in its ability to contract vascular smooth muscle. [1] The rank order of potency of the cysteinyl-leukotrienes to contract vascular smooth muscle is LTD4 > LTC4 > LTE4 >> LTF4. [1] [2] | |||
T15463 |
(Rac)-HAMI 3379
HAMI 3379 |
Others | Others |
HAMI 3379 is a potent and selective antagonist of the Cysteinyl leukotriene (CysLT2) receptor. HAMI 3379 has a protective effect on acute and subacute ischemic brain injury. It also attenuates microglia-related inflammation. | |||
T37386 |
Dihydro Montelukast
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Dihydro montelukast is a potential impurity found in commercial montelukast preparations. Montelukast (sodium salt) is a potent and selective cysteinyl leukotriene 1 (CysLT1) receptor antagonist. Formulations containing montelukast are used for the treatment of asthma as well as for the symptoms associated with allergic rhinitis. | |||
T21864 |
BAY-u 9773
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BAY-u 9773 是 CysLT 受体(半胱氨酸白三烯受体)的非选择性拮抗剂,对于 CysLT1和 CysLT2的 IC50值大致相同,用于抑制白三烯反应。 | |||
TP1816 |
Urotensin II, mouse
|
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Jump to search UTS2 Identifiers Aliases UTS2, PRO1068, U-II, UCN2, UII, urotensin 2 External IDs OMIM: 604097 MGI: 1346329 HomoloGene: 4939 GeneCards: UTS2 hide Gene location (Human) Chr. Chromosome 1 (human)[1] Band 1p36.23 Start 7,843,083 bp[1] En | |||
T72145 |
Montelukast dicyclohexylamine
MK0476 dicyclohexylamine |
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Montelukast (MK0476) dicyclohexylamine 是一种有效、选择性且具口服活性的半胱氨酸白三烯受体1 (CysLT1) 拮抗剂,用于哮喘和肝损伤预防研究。它在肠缺血-再灌注损伤中展现抗氧化作用,减轻心脏损伤,并降低嗜酸性粒细胞对哮喘气道的浸润。此外,亦被用于COVID-19的研究。 | |||
T37492 |
11-trans Leukotriene C4
11-trans Leukotriene C4 |
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11-trans Leukotriene C4 (11-trans LTC4) is a C-11 double bond isomer of LTC4. LTC4 undergoes slow temperature-dependent isomerization to 11-trans LTC4 during storage. 11-trans LTC4 is produced in smaller amounts relative to LTC4 in ionophore-stimulated HMC-1 cells (a human mast cell line) and equine eosinophils, but not in human neutrophils or RBL-1 cells. It is nearly equipotent with LTC4 for contraction of guinea pig parenchymal and ileum. In a radioligand binding assay using guinea pig ileum ... | |||
T37620 |
Leukotriene C4 methyl ester
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Leukotriene C4 (LTC4) is the parent cysteinyl-leukotriene produced by the LTC4 synthase-catalyzed conjugation of glutathione to LTA4. LTC4 is produced by neutrophils, macrophages, and mast cells, and by transcellular metabolism in platelets. It is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) and exhibits potent smooth muscle contracting activity. LTC4-induced bronchoconstriction and enhanced vascular permeability contribute to the pathogenesis of asthma and acute all... | |||
T60439 |
CAY10789
|
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CAY10789 (化合物 6) 是有效的CysLT1R 拮抗剂 ,IC50值为2.80 μM。CAY10789 也是一种GPBAR1激动剂 ,EC50为3 μM。CAY10789 显著降低 U937 细胞对 HAEC 的粘附并降低 TNF-α 的表达。CAY10789 表现出有前途的代谢稳定性和出色的药代动力学。 CAY10789 可用于结肠炎、代谢综合征和其他 GPBAR1/CysLT1R 相关疾病的研究。 | |||
T37980 |
N-methyl Leukotriene C4
N-methyl Leukotriene C4 |
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Produced by neutrophils, macrophages, mast cells, and by transcellular metabolism in platelets, leukotriene C4 (LTC4) is the parent cysteinyl leukotriene formed by the LTC4 synthase-catalyzed conjugation of glutathione to LTA4. It is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) and exhibits potent smooth muscle contracting activity. LTC4, however, is rapidly metabolized to LTD4 and LTE4, which makes the characterization of LTC4 pharmacology difficult. N-methyl Leukot... | |||
T83926 |
S-Geranylgeranyl-L-glutathione
GGG |
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S-Geranylgeranyl-L-glutathione是孤儿G蛋白偶联受体(GPCR)P2RY8的配体。该化合物在100 nM浓度下,选择性地诱导P2RY8而非鞘氨醇-1-磷酸受体2(S1P2)、GPR55、半胱氨酸白三烯受体1(CysLT1 receptor)以及CysLT2 receptor的内吞作用。在10 nM浓度下,S-Geranylgeranyl-L-glutathione抑制了表达P2RY8的WEHI-231 B细胞淋巴瘤细胞和分离的人扁桃体生发中心B细胞由趋化因子(C-X-C motif)配体12(CXCL12)诱导的迁移。 | |||
T38128 |
Leukotriene D4
Leukotriene D4 MaxSpec® Standard,LTD4 |
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Leukotriene D4 (LTD4) is one of the constituents of slow-reacting substance of anaphylaxis (SRS-A) produced by the metabolism of LTC4 by γ-glutamyl transpeptidase. It is the first cysteinyl-leukotriene metabolite of LTC4 . Like LTC4, LTD4-induced bronchoconstriction and enhanced vascular permeability contribute to the pathogenesis of asthma and acute hypersensitivity. LTD4 is equipotent to LTC4 in its biological activities, except that LTD4 is nearly 100-fold more effective in the contraction of... |
Cat. No. | Product Name | Target | Signaling Pathways |
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T1085 |
L-Glutathione reduced
谷胱甘肽,GSH,Isethion,Glutathione,γ-L-Glutamyl-L-cysteinyl-glycine,Glutathion,还原型谷胱甘肽,Tathion |
Ferroptosis; Reactive Oxygen Species; Endogenous Metabolite; Glutathione reductase | Apoptosis; Immunology/Inflammation; Metabolism; NF-κB; oxidation-reduction |
L-Glutathione reduced (Glutathione) 属于天然三肽,存在与细胞中,是一种内源性抗氧化剂,可以清除氧自由基。L-Glutathione reduced 是某些酶的辅助因子,参与蛋白质二硫键重排并减少过氧化物。 | |||
T4233 |
Cysteinylglycine
半胱氨酰甘氨酸,Cys-Gly |
Others; Endogenous Metabolite | Metabolism; Others |
Cysteinylglycine (Cys-Gly) 是内源性代谢产物的一种,能够用于疾病诊断。 | |||
TN4675 |
Nortrachelogenin
(-)-Wikstromol,(-)-Nortrachelogenin |
Apoptosis; Antifungal | Apoptosis; Microbiology/Virology |
Nortrachelogenin ((-)-Wikstromol) 可从 Partrinia scabiosaefolia 提取得到,具有抗真菌活性,可诱导膜破坏和半胱天冬酶依赖性细胞凋亡. | |||
TN2554 |
1-Monopalmitin
Glyceryl palmitate |
Apoptosis | Apoptosis |
1-Monopalmitin (Glyceryl palmitate) 是一种从Mougeotia nummuloides 和 Spirulina major 提取出来的小分子化合物,具有潜在的抗肿瘤活性,抑制A549和SPC-A1细胞增殖,诱导G2/M阻滞和半胱天冬酶依赖性细胞凋亡。 |