119
18
2
13
7
Cat. No. | Product Name | ||
---|---|---|---|
L9410 | 共价抑制剂库 | 1920 compounds | |
1920 种小分子的独特集合,包含已发现的共价抑制剂以及包含某些共价反应基团常见弹头的分子,如氯乙酰基,2-氯丙酰基,丙烯酰基,1-丙-2-炔基,1-丁-2-炔基,酮羰基,二硫键等,可以用于共价抑制剂药物研发; | |||
L9830 | 抗帕金森病化合物库 | 857 compounds | |
857 种帕金森病相关的化合物集合,可用于高通量和高内涵筛选; |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2086 |
ELN-441958
ELN 441958 |
Bradykinin Receptor | GPCR/G Protein |
ELN-441958是一种B1受体拮抗剂,能够抑制B1激动剂配体[3H] DAKD 与IMR-90细胞结合(Ki:0.26 nM),相较于B2受体,它对B1受体的抑制作用具有更高的选择性,且比抑制μ阿片受体选择性高500多倍,比抑制δ阿片受体选择性高2000多倍。 | |||
T15430 |
GSK2256294A
GSK 2256294 |
Others; Epoxide Hydrolase | Metabolism; Others |
GSK2256294A (GSK 2256294) 是重组人、大鼠和小鼠 sEH 的有效特异性抑制剂,IC50 分别为 27 pM、61 pM 和 189 pM。 | |||
T21995 |
XAP044
|
GluR | Neuroscience |
XAP044 是高效的选择性mGlu7拮抗剂。代谢型谷氨酸受体亚型 7 是哺乳动物 CNS 中神经传递的重要突触前调节剂。它在啮齿动物行为测试中表现出较好的大脑暴露、广谱抗应激、抗抑郁以及抗焦虑作用。 | |||
T1812 |
KX1-004
KX1 004,KX1004 |
Src | Angiogenesis; Tyrosine Kinase/Adaptors |
KX1-004 是非 ATP 竞争性 Src-PTK 抑制剂,IC50=40 μM。它能够保护耳蜗,使其免受有害噪音的影响,并防止噪音引起的听力损失 (NIHL)。 | |||
T20039 |
7-Methyladenine
NSC7857,7-甲基腺嘌呤,NSC-7857,NSC 7857 |
Others | Others |
7-Methyladenine (NSC-7857) 可用作暴露于外源性和致癌性甲基化剂的标志物。 | |||
T0601 |
Monobenzyl phthalate
邻苯二甲酸单苄酯,Phthalic Acid Monobenzyl Ester |
Others; Endogenous Metabolite | Metabolism; Others |
Phthalic Acid Monobenzyl Ester 是一种暴露于邻苯二甲酸盐(如,邻苯二甲酸二乙基己酯)后的尿代谢物 (urinary metabolite),具有雌激素作用。。 | |||
T8547 |
DCBA
|
Drug Metabolite | Metabolism |
DCBA 是驱虫剂 N-N-diethyl-meta-toluamide (DEET) 的代谢物。尿液中 DCBA 的浓度是评估 DEET 暴露程度的指标。 | |||
T36478 |
BI-6901
|
CCR | Immunology/Inflammation; Microbiology/Virology |
BI-6901 是一种选择性 CCR10 拮抗剂。在DNFB接触超敏反应的小鼠模型中,BI 6901 以剂量依赖的方式显示其抗炎反应。 | |||
TQ0039 |
(±)-Zanubrutinib
(±)-BGB-3111 |
BTK | Angiogenesis; Tyrosine Kinase/Adaptors |
(±)-Zanubrutinib ((±)-BGB-3111) 是一种有效的口服Bruton’s 酪氨酸激酶(Btk)抑制剂,具有优越的口服生物利用度,可实现更高的暴露量和更完整的靶点抑制。 | |||
T19310 |
Ensulizole
2-PHENYLBENZIMIDAZOLE-5-SULFONIC ACID,苯基苯丙咪唑磺酸,2-Phenyl-1H-benzo[d]imidazole-5-sulfonic acid,Phenylbenzimidazole sulfonic acid |
Others | Others |
Ensulizole 是磺化的紫外线吸收剂,可以强烈吸收 UVB 和部分 UVA。在紫外线或阳光照射下,它可以产生活性氧,进而破坏 DNA。 | |||
T0976 |
Propoxur
残杀威,Aprocarb,Propoxure,Baygon |
AChR; Antifungal | Microbiology/Virology; Neuroscience |
Propoxur (Propoxure) 是一种氨基甲酸酯类杀虫剂,用于控制蟑螂、苍蝇、蚊子以及草坪和草坪昆虫。 | |||
T3106 |
C-DIM12
|
Apoptosis; Others | Apoptosis; Others |
C-DIM12是一种人工合成的Nurr1激活剂,可诱导Nurr1和DA 基因表达。 | |||
T35501 |
5,6-trans-Vitamin D3
5,6-trans-Colecalciferol,5,6-trans-Cholecalciferol,Cholecalciferol EP Impurity A |
Vitamin | Metabolism |
5,6-trans-Vitamin D3(5,6-trans-Cholecalciferol)是维生素 D3 的异构体,经光照后在皮肤表面由 Vitamin D3 转化而来。 | |||
T17315 |
(±)-CPSI-1306
cpsi-1306,2-(3-(2,4-Difluorophenyl)-4,5-dihydroisoxazol-5-yl)-1-morpholinoethan-1-one |
Others | Others |
(±)-CPSI-1306 (2-(3-(2,4-Difluorophenyl)-4,5-dihydroisoxazol-5-yl)-1-morpholinoethan-1-one) 是一种巨噬细胞迁移抑制因子 (MIF) 拮抗剂,可用于关于非胰岛素依赖型糖尿病 (NIDDM) 的研究以及预防急性和慢性 UVB 暴露对皮肤的有害影响。 | |||
T21404 |
Fluticasone furoate
Veramyst,Allermist,Avamys,糠酸氟替卡松,Fluticasone furoate |
Glucocorticoid Receptor | Endocrinology/Hormones |
Fluticasone furoate (Avamys) 是一种合成的三氟化皮质类固醇,衍生自氟替卡松,Kd 为 0.3 nM。Fluticasone furoate 具有有效的抗炎、抗哮喘活性和低全身暴露。Fluticasone furoate 可用作过敏性鼻炎治疗研究的鼻喷雾剂。 | |||
T22341 |
GSK-114
|
Others | Others |
GSK 114 是口服有活性的、高选择性的TNNI3K 抑制剂 (IC50= 25 nM)。其中TNNI3K (又称 CARK) 是酪氨酸样激酶家族的成员,选择性在心脏组织中表达。它对 TNNI3K 的选择性是 B-Raf 激酶的 40 倍 (IC50= 1 µM)。 | |||
T0357 |
Potassium iodide
|
Tyrosinase | Proteases/Proteasome |
Potassium iodide 用于治疗过度活跃的甲状腺,并保护甲状腺免受吞咽或吸入放射性碘的辐射影响。可在意外接触放射性碘后或服用含放射性碘的药物前后使用。 | |||
TP1179L |
Porcine dynorphin A(1-13) acetate
Dynorphin A Porcine Fragment 1-13 acetate,Porcine dynorphin A(1-13) acetate(72957-38-1 free base) |
Opioid Receptor | Endocrinology/Hormones; GPCR/G Protein; Neuroscience |
Porcine dynorphin A(1-13) acetate (Dynorphin A Porcine Fragment 1-13 acetate)(72957-38-1 free base) 是一种有效的内源性 κ opioid 受体激动剂,在生理浓度下具有镇痛作用。暴露于强啡肽 A (1-13) 会导致单个神经元中 [Ca2+]i 的急剧增加,类似于急性 NMDA 治疗所见的增加。 | |||
T1435 |
Praziquantel
吡喹酮,Pyquiton,Droncit,Biltricide |
Calcium Channel; Antibiotic; Parasite | Membrane transporter/Ion channel; Metabolism; Microbiology/Virology |
Praziquantel (Droncit) 是一种外消旋混合物,由 (R)-Praziquantel 和 (S)-Praziquantel 组成。它可研究血吸虫病。 | |||
T1787 |
Levobupivacaine
|
Sodium Channel | Membrane transporter/Ion channel |
Levobupivacaine 是一种氨基酰胺类局麻药,属于n-alkylsubstituted pipecoloxylidide 家族。它是bupivacaine 的 S-对映异构体。 | |||
T38003 |
Levofloxacin N-oxide
|
Others | Others |
Levofloxacin N-oxide 是从左氧氟沙星中分离出来的杂质。 | |||
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。 | |||
T39136 |
ATX inhibitor 7
|
Others | Others |
ATX inhibitor 7 is a autotaxin inhibitor and shows good oral exposure. | |||
T8675 |
Vaniprevir
|
Others | Others |
Vaniprevir is a macrocyclic hepatitis C virus NS3/4a protease inhibitor and is active against both the genotype 1 and genotype 2 NS3/4a protease enzymes. vaniprevir has good plasma exposure and excellent liver exposure in multiple species. | |||
T26525 |
ABT-281
ABT 281,A-86281,A 86281,ABT281,A86281 |
Others | Others |
ABT-281 is an ascomycin analog and a macrolactam T cell inhibitors with potent topical activity and reduced systemic exposure. | |||
T34777 |
Talaporfin free acid
Monoaspartyl chlorin,NPe6,Talaporfin,Aspartyl chlorin |
Others | Others |
Talaporfin, an effective tumor localizer, can produce the selective degradation of tumor tissue following light exposure. | |||
T29689 |
AFB1-N7-guanine
|
Others | Others |
In epidemiological studies, Aflatoxin B1-N7-guanine serum albumin adducts have been established as biomarkers of dietary aflatoxin exposure. | |||
T71091 |
Y2-Antagonist-2
|
Others | Others |
Y2-Antagonist-2 is a novel, selective, soluble non-peptidic NPY Y2 receptor antagonist with enhanced CNS exposure. | |||
T68335 |
MK-1220
|
Others | Others |
MK-1220 is a novel Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma Exposure. | |||
T70223 |
UA8967
|
Others | Others |
UA8967 is a membrane-active anti-tumor agent. Cytotoxicity studies in six pancreatic cancer cell lines, one normal human pancreatic ductal epithelial line and two colon cancer cells showed the IC50s UA8967 ranged from 12–61 μM for exposure times of 72 h. There was also no selective inhibition of DNA, RNA or protein synthesis after exposure to UA8967. UA8967 is observed to affect the plasma membrane. | |||
T14879 | CB 300919 | Others | Others |
CB 300919 is a quinazoline-based antitumor agent with high activity in the CH1 human ovarian tumor xenograft and has continuous exposure (96 h) growth inhibition (IC50: 2 nM). | |||
T16372 |
Obidoxime dichloride
|
Others | Others |
Obidoxime dichloride, a selective oxime agent, effectively reactivates sarin-inhibited acetylcholinesterase (AChE) and mitigates the acute toxicity associated with sarin exposure. It is also utilized as an antidote for organophosphate nerve agent poisoning. | |||
T6060L |
Anabasine HCl
BB-NC-0036,CCG-38440,H-8174,AR-1H7273,ZX-BK000320,ST-24041653 |
Others | Others |
Anabasine HCl is used as a clinical biomarker for tobacco smoke exposure and as an insecticide. It is also a depolarizing NMJ blocker, aromatase inhibitor, nAChr antagonist, and teratogen found in species of Nicotiana. | |||
T30691 |
Calcium diglutamate
Calcium di-L-glutamate,Glutamic acid, calcium salt (2:1), L- |
Others | Others |
Calcium diglutamate(CDG), calcium acid salt of glutamic acid. As a soluble source of calcium ions, this chemical is used as a first-aid treatment for exposure to hydrofluoric acid. | |||
T35236 |
5α-Hydroxy-6-keto cholesterol
YS 64,Yakkasterone,5α-羟基-6-酮胆固醇 |
Others | Others |
Yakkasterone is a major metabolite of cholesterol formed during exposure of lung epithelial cells to ozone. | |||
T69607 |
Dersimelagon phosphate
|
Others | Others |
Dersimelagon phosphate is a selective melanocortin-1 receptor (MC1R) agonist that increases skin melanin without sun exposure and is being developed to increase light tolerance in EPP/XLP patients. | |||
T61174 |
MT-134
|
Others | Others |
MT-134 是一种 SkMII 特异性抑制剂,在肌肉中具有良好的暴露性。 | |||
T70608 |
cis-Entacapone
|
Others | Others |
cis-Entacapone is a metabolite of the catechol-O-methyltransferase (COMT) inhibitor entacapone. It is also a potential impurity found in commercial preparations of entacapone and a degradant of entacapone formed by UV light exposure. | |||
T14570 |
BI 99179
BI99179 |
Fatty Acid Synthase | Metabolism |
BI99179 is a potent and selective type I fatty acid synthase (FAS) inhibitor with an IC50 of 79 nM and it exhibits significant exposure (both peripheral and central) upon oral administration in rats[1]. | |||
T35458 |
(R)-nitro-Blebbistatin
|
Others | Others |
(R)-nitro-Blebbistatin is a more stable form of (+)-blebbistatin , which is the inactive form of (-)-blebbistatin . Prolonged exposure to blue light (450-490 nm) results in degradation of blebbistatin to an inactive product via cytotoxic intermediates, which may be problematic for its use in fluorescent live cell imaging applications. The addition of a nitro group stabilizes the molecule to circumvent its degradation by prolonged blue light exposure. (R)-nitro-Blebbistatin has the same stereoche... | |||
T26573 |
AG311
AG 311,AG-311 |
Others | Others |
AG311 is an inhibitor of complex I and hypoxia-induced HIF-1α stabilization. In vitro, AG311 induces rapid necrosis in numerous cancer cell lines. Within minutes, exposure to AG311 also results in mitochondrial depolarization, superoxide production, and i | |||
T31194 |
Dalapon
Basfapon B,Dowpon M,Dawpon-Rae |
Others | Others |
Dalapon is a selective herbicide used to control perennial grasses. The major use of dalapon is on food crops including sugarcane and sugar beets. Its use is no longer authorized in France. The National Institute for Occupational Safety and Health in the | |||
T38267 |
Valeryl-L-carnitine (chloride)
Valeryl-L-carnitine (chloride),L-Valerylcarnitine |
Others | Others |
Valeryl-L-carnitine is a short-chain acylcarnitine and a derivative of L-carnitine . Valeryl-L-carnitine levels increase in the serum of rhesus monkeys following exposure to 7 and 10 Gray units (Gy) of ionizing radiation.[1] | |||
T40397 |
3,4,6-Trichlorocatechol
|
Others | Others |
3,4,6-Trichlorocatechol (TCC) is a metabolite generated by the post-mitochondrial liver fraction in Aroclor-1254 induced rats, resulting from exposure to industrial pollutants. | |||
T26821 |
BIPM
|
Others | Others |
BIPM is a potent inhibitor of Rho-associated protein kinase 2 (ROCK2). Exposure of SH-SY5Y cells to BIPM led to significant changes in cell migration, actin stress fibers and neurite length. BIPM significantly inhibits phosphorylation of cofilin, a regula | |||
T37704 |
Olanzapine Lactam Impurity
|
Others | Others |
Olanzapine lactam impurity is a potential impurity found in commercial preparations of olanzapine.1It is a degradation product formed by exposure to thermal or oxidative stress. 1.Baertschi, S.W., Brunner, H., Bunnell, C.A., et al.Isolation, identification, and synthesis of two oxidative degradation products of olanzapine (LY170053) in solid oral formulationsJ. Pharm. Sci.97(2)883-892(2008) | |||
T40226 |
FP-Biotin
|
Others | Others |
FP-biotin is a potent organophosphorus toxicant, ideal for identifying novel biomarkers of organophosphorus toxicant exposure. It measures FAAH, ABHD6, and MAG-lipase activity, specifically in plasma studies, due to the efficient purification of biotinylated peptides through binding to immobilized avidin beads. | |||
T85274 |
2-hydroxy Myristic Acid methyl ester
|
Others | Others |
2-Hydroxy Myristic Acid Methyl Ester, a rare hydroxylated fatty acid methyl ester isolated from aquatic microbial sources, experiences a decrease in levels to <1% within these communities following Atradex pesticide exposure at 245 mg/L concentration. [Matreya, LLC. Catalog No. 1704] | |||
T85217 |
Cholesteryl Palmitoleate
Cholesterol Palmitoleate,16:1(9Z) Cholesterol ester,CE(16:1),16:1(9Z) CE |
Others | Others |
Cholesteryl palmitoleate, a cholesterol ester, exhibits elevated plasma levels in ApoE-/- mice following exposure to cigarette smoke and in pediatric patients diagnosed with biliary atresia. It serves as a standard for identifying cholesterol esters in human meibomian gland secretions. | |||
T11986 |
Mebeverine acid
Mebeverine metabolite Mebeverine acid,美贝维林酸 |
Drug Metabolite | Metabolism |
Mebeverine acid (Mebeverine metabolite Mebeverine acid) 是美贝维林的次级代谢产物,可用作口服美贝维林的标志物。 |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
TN7118 |
Methylhippuric acid
Methyl hippurate,N-苯甲酰基甘氨酸甲酯 |
||
Methylhippuric acid (Methyl hippurate) 是人体尿液中二甲苯暴露的生物标志物。 | |||
T4931 |
Dihydroxyfumaric acid hydrate
|
Others; Endogenous Metabolite | Metabolism; Others |
Dihydroxyfumaric acid hydrate 是内源性代谢产物的一种。 | |||
T5S1550 |
Cinnamyl alcohol
肉桂醇,肉桂醇;beta-苯丙烯醇,Cinnamic Alcohol,Styryl Carbinol |
PPAR | DNA Damage/DNA Repair; Metabolism |
Cinnamyl alcohol (Styryl Carbinol) 是从板栗花中分离得到的一种活性成分,抑制增加的 PPARγ表达,具有抗肥胖作用。 | |||
T19082 |
1-Hydroxypyrene
1-Pyrenol,Pyren-1-ol,1-羟基芘 |
Endogenous Metabolite | Metabolism |
1-Hydroxypyrene (1-Pyrenol) 是一种暴露于多环芳烃的生物标志物,存在尿液样本中,也是一种暴露于 pyrenes 中的主要生物标志物。 | |||
T5718 |
L-(+)-Abrine
L-(+)-红豆碱,L-N-Methyltryptophan,N-α-Methyl-L-tryptophan,L-ABRINE |
Others | Others |
L-(+)-Abrine (L-N-Methyltryptophan) 是一种致命白蛋白,发现于在 Abrus precatorius 种子中,是一种急性毒性生物碱,可用作化学标记物。 | |||
T3746 |
Dimethyl phthalate
邻苯二甲酸二甲酯,Solvanom,Avolin,Fermine,避蚊酯 |
Others | Others |
Dimethyl phthalate (Fermine) 是一种邻苯二甲酸酯 (PAEs),是一种已知的内分泌干扰物,也是一种普遍存在的污染物。它常作为增塑剂,赋予硬质聚氯乙烯 (PVC) 树脂以柔韧性。 | |||
T1659 |
Melatonin
Melatonine,松果体素,N-Acetyl-5-methoxytryptamine,褪黑素 |
CaMK; Apoptosis; Mitophagy; Estrogen/progestogen Receptor; Melatonin Receptor; Glutathione Peroxidase; Endogenous Metabolite; ROR; Autophagy | Apoptosis; Autophagy; Endocrinology/Hormones; GPCR/G Protein; Metabolism; Neuroscience |
Melatonin (Melatonine) 是一种由松果体制成的激素,可激活褪黑激素受体。它在睡眠中起作用,有抗氧化和抗炎特性。它是新型选择性ATF-6抑制剂,可诱导细胞凋亡。 | |||
T4787 |
2-Hydroxyisobutyric acid
2-甲基-2-羟基丙酸,α-Hydroxyisobutyric acid |
Others; Endogenous Metabolite | Metabolism; Others |
2-Hydroxyisobutyric acid (α-Hydroxyisobutyric acid) 是内源性代谢产物的一种。 | |||
T2S0633 |
Raspberry ketone
Oxyphenalon,Rasketone,Aloenin,4-(4-Hydroxyphenyl)-2-butanone,p-Hydroxybenzyl acetone,Frambinone,覆盆子酮 |
PPAR | DNA Damage/DNA Repair; Metabolism |
Raspberry ketone (p-Hydroxybenzyl acetone) 是覆盆子中主要的芳香族天然产物,主要用作化妆品的香料和食品增味剂,也可作 PPAR-α激动剂。 | |||
T5S0018 |
Betulonic acid
路路通酸,(+)-Betulonic acid,Betunolic acid,Liquidambaric acid |
Parasite; HSV | Microbiology/Virology |
Betulonic acid (Liquidambaric acid) 是一种在许多植物中存在的三萜类天然产物,具有抗肿瘤,抗炎,抗寄生虫和抗病毒的活性。 | |||
T6S1917 |
Schisandrol B
Gomisin A,TJN-101,Besigomsin,五味子醇乙,Gamma-Schisandrin,戈米辛A,Schizandrol B,Wuweizi alcohol-B |
P450; Reactive Oxygen Species; Autophagy | Autophagy; Immunology/Inflammation; Metabolism; NF-κB |
Schisandrol B (Besigomsin) 是华中五味子的主要活性成分,具有保肝、抗炎、抗糖尿病和抗氧化的作用。它抑制活性氧的产生,也抑制 P-糖蛋白和CYP3A 的活性。 | |||
T3S0013 |
Ethyl trans-caffeate
咖啡酸乙酯,Ethyl caffeate,Caffeic Acid Ethyl Ester |
Others | Others |
Ethyl trans-caffeate (Caffeic Acid Ethyl Ester) 具有抗炎作用。 它是一种有前途的天然化合物,未来在慢性肝病中的应用。它是一种有效的化学预防化合物,可防止因太阳紫外线照射引起的皮肤癌变。它是与人胰腺α-淀粉酶复合的代表性抑制剂的高分辨率结构。 它强烈抑制 JB6 Cl41细胞的肿瘤转化,无毒性。 PI3K、ERK1/2 和 p38 激酶活性在体外通过与 HOEC 直接结合而受到抑制。 | |||
T37280 |
PE(18:1(9Z)/0:0)
|
Endogenous Metabolite | Metabolism |
PE(18:1(9Z)/0:0) 是一种天然存在的溶血磷脂,是缩醛磷脂溶血磷脂酰乙醇胺的类似物。 PE(18:1(9Z)/0:0) 以浓度依赖性方式诱导 PC12 大鼠神经元细胞中细胞内钙的瞬时增加。 PE(18:1(9Z)/0:0) 增加 IL-4 和 IL-2 的产生,但不增加 IFN-γ 的产生。 在小鼠血清中,PE(18:1(9Z)/0:0)(1 μg/动物)诱导 T 辅助细胞 2 反应。 在寒冷暴露三天后,小鼠肩胛间棕色脂肪组织中的 PE(18:1(9Z)/0:0) 水平增加。 | |||
TN4026 |
Eucamalol
|
Others | Others |
Eucamolol exhibits significant repellent activity against Aedes albopictus, and inhibits its feeding as well as DEET, is effective repellent (75%) up to 3 h after exposure to mosquito. | |||
TN1766 |
(-)-Integerrimine
Integerrimine,全緣千里光鹼,全缘千里光碱 |
Others | Others |
Prenatal exposure to Integerrimine N-oxide induces maternal toxicity, impairment of maternal care and delayed in physical and behavioral development of the offspring. Doses of Integerrimine N-oxide here employed did not produce marked immunotoxic effects. | |||
T83108 |
Anhuienoside B
|
Others | Others |
Anhuienoside B为从C. anhuiensis K. F. Wu鲜叶中提取的天然产物,能应对CuCl2诱导的非生物胁迫。 | |||
T40859 |
5-Hydroxy-8-methoxypsoralen
5-Hydroxyxanthotoxin,5-Hydroxy-8-methoxypsoralen |
Others | Others |
5-Hydroxy-8-methoxypsoralen (5-Hydroxyxanthotoxin) is a metabolite derived from Xanthotoxin, which acts as a potent tricyclic furocoumarin suicide inhibitor of CYP (cytochrome P-450). It is employed as an agent for the treatment of psoriasis, eczema, vitiligo, and certain cutaneous Lymphomas, in combination with phototherapy involving exposure to sunlight. | |||
T80950 |
Tricetin 7-O-glucoside
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Tricetin 7-O-glucoside (compound 33)为一种黄酮类单-O-糖苷。 |
Cat. No. | Product Name | Species | Expression System |
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TMPY-03407 |
NQO1 Protein, Human, Recombinant (His)
NAD(P)H dehydrogenase, quinone 1,NMORI,DIA4,QR1,NMOR1,DTD,DH... |
Human | E. coli |
NQO1 gene is a member of the NAD(P)H dehydrogenase (quinone) family and encodes a cytoplasmic 2-electron reductase. NQO1 forms homodimers and reduces quinones to hydroquinones. NQO1's enzymatic activity prevents the one-electron reduction of quinones that results in the production of radical species. Mutations in the NQO1 gene have been associated with tardive dyskinesia (TD), an increased risk of hematotoxicity after exposure to benzene, and susceptibility to various forms of cancer. Altered ex... | |||
TMPH-02153 |
Sulfiredoxin-1 Protein, Human, Recombinant (His & Myc)
SRXN1,Sulfiredoxin-1 |
Human | E. coli |
Contributes to oxidative stress resistance by reducing cysteine-sulfinic acid formed under exposure to oxidants in the peroxiredoxins PRDX1, PRDX2, PRDX3 and PRDX4. Does not act on PRDX5 or PRDX6. May catalyze the reduction in a multi-step process by acting both as a specific phosphotransferase and a thioltransferase. | |||
TMPK-00516 |
BST1 Protein, Cynomolgus, Recombinant (His)
Bp-3,CD157,Bst1,BST-1,Ly65,Bp3,Antigen BP3 |
Cynomolgus | HEK293 Cells |
BST1 overexpression conferred resistance to sphingosine in yeast. BST1 deletion produced sensitivity to exogenous D-erythro-sphingosine and phytosphingosine and intracellular accumulation of sphingosine 1-phosphate upon exposure to exogenous sphingosine. sphingoid base metabolism is similar in all eukaryotes and suggests that yeast genetics may be useful in the isolation and identification of other genes involved in sphingolipid signaling and metabolism. | |||
TMPH-01676 |
Meteorin-like/METRNL Protein, Human, Recombinant (His & SUMO)
METRNL,Meteorin-like protein,Subfatin |
Human | E. coli |
Hormone induced following exercise or cold exposure that promotes energy expenditure. Induced either in the skeletal muscle after exercise or in adipose tissue following cold exposure and is present in the circulation. Able to stimulate energy expenditure associated with the browning of the white fat depots and improves glucose tolerance. Does not promote an increase in a thermogenic gene program via direct action on adipocytes, but acts by stimulating several immune cell subtypes to enter the a... | |||
TMPH-03614 |
DNA photolyase Protein, Synechococcus sp., Recombinant (His & Myc & SUMO)
DNA photolyase,Deoxyribodipyrimidine photo-lyase,phr,phrA,Ph... |
Synechococcus | E. coli |
Involved in repair of UV radiation-induced DNA damage. Catalyzes the light-dependent monomerization (300-600 nm) of cyclobutyl pyrimidine dimers (in cis-syn configuration), which are formed between adjacent bases on the same DNA strand upon exposure to ultraviolet radiation. DNA photolyase Protein, Synechococcus sp., Recombinant (His & Myc & SUMO) is expressed in E. coli expression system with N-10xHis-SUMO and C-Myc tag. The predicted molecular weight is 74.3 kDa and the accession number is P05... | |||
TMPJ-01107 |
PAP Protein, Human, Recombinant (His)
PAP1,PAP,PDGFA-Associated Protein 1,HASPP28,28 kDa Heat- and... |
Human | E. coli |
Human PAP, also known as 28 kDa heat- and acid-stable phosphoprotein, PDGF-associated protein, PDGFA-associated protein 1, PDAP1, HASPP28, is a protein which belongs to the PDAP1 family. The encoded protein in rodents has been shown to bind PDGFA with a low affinity. PDGF-Associated Protein (PAP) is a phosphoprotein that may enhance PDGFA-stimulated cell growth in fibroblasts, but inhibits the mitogenic effect of PDGFB. PDAP1 expression is induced by TNF-alpha, and cells overexpressing PDAP1 sho... | |||
TMPJ-00018 |
CCL16 Protein, Human, Recombinant
NCC-4,Lymphocyte and Monocyte Chemoattractant,LMC,NCC4,HCC-4... |
Human | E. coli |
CCL16 is a member of CC chemokine family. CCL16 cDNA encodes a 120 amino acid peptide along with a 23 amino acids signal peptide that is cleaved to generate 97 amino acid protein. CCL16 is distantly related to other CC chemokines, showing less than 30% sequence identity. CCL16 elicits its effects on cells by interacting with cell surface chemokine receptors such as CCR1, CCR2, CCR5 and CCR8. Recombinant CCL16 has been shown to chemoattract human monocytes and THP1 cells but not resting lymphocyt... | |||
TMPH-00201 |
BK polyomavirus (BKPyV) VP2 Protein (His)
Minor capsid protein VP2,Minor structural protein VP2 |
BKPyV | E. coli |
Isoform VP2 is a structural protein that resides within the core of the capsid surrounded by 72 VP1 pentamers. Participates in host cell receptor binding together with VP1. Following virus endocytosis and trafficking to the endoplasmic reticulum, VP2 and VP3 form oligomers and integrate into the endoplasmic reticulum membrane. Heterooligomer VP2-VP3 may create a viroporin for transporting the viral genome across the endoplasmic reticulum membrane to the cytoplasm. Nuclear entry of the viral DNA ... | |||
TMPY-03851 |
BPIFB1 Protein, Human, Recombinant (His)
LPLUNC1,BPI fold containing family B, member 1,C20orf114 |
Human | HEK293 Cells |
BPIFB1, also known as LPLUNC1, belongs to the BPI/LBP/Plunc superfamily, plunc family. BPIFB1 may be involved in the innate immune response to bacterial exposure in the mouth, nasal cavities, and lungs. BPIFB1 is expressed in the upper respiratory tract and oral cavity, which may function in host defence. The expression of BPIF proteins is associated with CF lung disease in humans and mice. It is unclear if this elevation of protein production, which results from phenotypic alteration of the cel... | |||
TMPH-02365 |
JC polyomavirus (JCV) Minor capsid protein VP2 (His)
Minor capsid protein VP2,Minor structural protein VP2 |
JCPyV | E. coli |
Isoform VP2 is a structural protein that resides within the core of the capsid surrounded by 72 VP1 pentamers. Participates in host cell receptor binding together with VP1. Following virus endocytosis and trafficking to the endoplasmic reticulum, VP2 and VP3 form oligomers and integrate into the endoplasmic reticulum membrane. Heterooligomer VP2-VP3 may create a viroporin for transporting the viral genome across the endoplasmic reticulum membrane to the cytoplasm. Nuclear entry of the viral DNA ... | |||
TMPJ-00748 |
Ig kappa Protein, Human, Recombinant (His)
Ig κ chain C region AG,Ig κ,Ig kappa chain C region AG,Ig ka... |
Human | HEK293 Cells |
Immunoglobulin Kappa is constant region of immunoglobulin light chains. Immunoglobulins, also known as antibodies, are membrane-bound or secreted glycoproteins produced by B lymphocytes. In the recognition phase of humoral immunity, the membrane-bound immunoglobulins serve as receptors which, upon binding of a specific antigen, trigger the clonal expansion and differentiation of B lymphocytes into immunoglobulins-secreting plasma cells. Secreted immunoglobulins mediate the effector phase of humo... | |||
TMPH-00789 |
Hamster polyomavirus (HaPyV) VP1 Protein (His & Myc)
Major structural protein VP1,Major capsid protein VP1 |
HaPyV | E. coli |
Forms an icosahedral capsid with a T=7 symmetry and a 40 nm diameter. The capsid is composed of 72 pentamers linked to each other by disulfide bonds and associated with VP2 or VP3 proteins. Interacts with sialic acids on the cell surface to provide virion attachment to target cell. Once attached, the virion is internalized by endocytosis and traffics to the endoplasmic reticulum. Inside the endoplasmic reticulum, the protein folding machinery isomerizes VP1 interpentamer disulfide bonds, thereby... | |||
TMPJ-00837 |
LAMP1 Protein, Mouse, Recombinant (His)
Lysosomal membrane glycoprotein A,CD107a,LAMP-1,CD107 antige... |
Mouse | HEK293 Cells |
Lysosomal associated membrane protein 1 (LAMP1) is an approximately 120 kDa transmembrane glycoprotein that is a major protein component of lysosomal membranes. Mature mouse LAMP1 consists of a 346 amino acid (aa) intralumenal domain (ECD), a 24 aa transmembrane segment, and a 12 aa cytoplasmic tail. Its lumenal domain is organized into two heavily N-glycosylated regions separated by a Ser/Pro-rich linker that carries a minor amount of O-linked glycosylation. Within the lumenal domain, mouse LAM... |
Cat. No. | Product Name | Target | Signaling Pathways |
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TMIH-0322 |
Mebeverine Acid-d5
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Mebeverine Acid-d5 是 Mebeverine Acid 的氘代化合物。Mebeverine Acid 的 CAS 号为 475203-77-1。Mebeverine acid 是美贝维林的次级代谢产物,可用作口服美贝维林的标志物。 | |||
TMIJ-0526 |
Dibutyl Phthalate-d4
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Dibutyl Phthalate-d4 是 Dibutyl Phthalate 的氘代化合物。Dibutyl Phthalate 的 CAS 号为 84-69-5。Dibutyl phthalate 是一种用于大多数塑料的增塑剂,存在于水、空气、土壤、植物和动物中。长期接触可能会产生一些不利影响。 | |||
TMIJ-0412 |
Phthalic acid, bis-isobutyl ester-d4
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Phthalic acid, bis-isobutyl ester-d4 是 Phthalic acid, bis-isobutyl ester 的氘代化合物。Phthalic acid, bis-isobutyl ester 的 CAS 号为 84-69-5。Dibutyl phthalate 是一种用于大多数塑料的增塑剂,存在于水、空气、土壤、植物和动物中。长期接触可能会产生一些不利影响。 | |||
TMIJ-0505 |
Fluticasone Furoate-d3
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Fluticasone Furoate-d3 是 Fluticasone Furoate 的氘代化合物。Fluticasone Furoate 的 CAS 号为 397864-44-7。Fluticasone furoate 是一种合成的三氟化皮质类固醇,衍生自氟替卡松,Kd 为 0.3 nM。Fluticasone furoate 具有有效的抗炎、抗哮喘活性和低全身暴露。Fluticasone furoate 可用作过敏性鼻炎治疗研究的鼻喷雾剂。 | |||
TMID-0153 |
MELATONIN(ACETYL-d3)
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MELATONIN(ACETYL-d3) 是 MELATONIN 的氘代化合物。MELATONIN 的 CAS 号为 73-31-4。Melatonin 是一种由松果体制成的激素,可激活褪黑激素受体。它在睡眠中起作用,有抗氧化和抗炎特性。它是新型选择性ATF-6抑制剂,可诱导细胞凋亡。 | |||
T35517 |
4-deoxy Nivalenol-13C15
4-deoxy Nivalenol-13C15 |
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4-deoxy Nivalenol-13C15is intended for use as an internal standard for the quantification of 4-deoxy nivalenol by GC- or LC-MS. 4-deoxy Nivalenol is a trichothecene mycotoxin that has been found inFusarium.1It binds to eukaryotic ribosomes and inhibits protein synthesis in mice when administered at doses ranging from 5 to 25 mg/kg. 4-deoxy Nivalenol (0.1 and 0.2 mg/kg) induces emesis in pigs and decreases feed consumption in pigs when administered at a dose of 40 ppb in the diet.2It induces leth... | |||
T35775 |
HT-2 Toxin-13C22
HT-2 Toxin-13C22 |
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HT-2 toxin-13C22is intended for use as an internal standard for the quantification of HT-2 toxin by GC- or LC-MS. HT-2 toxin is a type A trichothecene mycotoxin and an active, deacetylated metabolite of the trichothecene mycotoxin T-2 toxin .1,2Like T-2 toxin, HT-2 toxin inhibits protein synthesis and cell proliferation in plants.2HT-2 toxin also reduces viability of HepG2, A549, HEp-2, Caco-2, A-204, U937, Jurkat, and RPMI-8226 cancer cells with IC50values ranging from 3.1 to 23 ng/ml and human... |