111
19
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T37547 |
trans-Urocanic Acid
|
||
trans-Urocanic acid is a major epidermal chromophore for the immunosuppressive effects of UV radiation that is produced in mammalian stratum corneum by the action of histidine ammonialyase on L-histidine. It contributes to the acidification of the surface of the stratum corneum, and its function has been proposed as that of an endogenous sunscreen, endowing a low-level of protection (SPF ~ 1.5) against UV-induced DNA damage and excessive keratinocyte apoptosis. Upon UVB exposure, trans-urocanic ... | |||
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。 | |||
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。 | |||
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。 | |||
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. | |||
T39136 |
ATX inhibitor 7
|
||
ATX inhibitor 7 is a autotaxin inhibitor and shows good oral exposure. | |||
T34777 |
Talaporfin free acid
Monoaspartyl chlorin,NPe6,Talaporfin,Aspartyl chlorin |
||
Talaporfin, an effective tumor localizer, can produce the selective degradation of tumor tissue following light exposure. | |||
T71091 |
Y2-Antagonist-2
|
||
Y2-Antagonist-2 is a novel, selective, soluble non-peptidic NPY Y2 receptor antagonist with enhanced CNS exposure. | |||
T26525 |
ABT-281
ABT 281,A-86281,A 86281,ABT281,A86281 |
||
ABT-281 is an ascomycin analog and a macrolactam T cell inhibitors with potent topical activity and reduced systemic exposure. | |||
T29689 |
AFB1-N7-guanine
|
||
In epidemiological studies, Aflatoxin B1-N7-guanine serum albumin adducts have been established as biomarkers of dietary aflatoxin exposure. | |||
T68335 |
MK-1220
|
||
MK-1220 is a novel Macrocyclic Inhibitor of Hepatitis C Virus NS3/4A Protease with Improved Preclinical Plasma Exposure. | |||
T70223 |
UA8967
|
||
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 |
||
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. | |||
T69607 | Dersimelagon phosphate | ||
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. | |||
T30691 |
Calcium diglutamate
Calcium di-L-glutamate,Glutamic acid, calcium salt (2:1), L- |
||
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. | |||
T61174 | MT-134 | ||
MT-134 是一种 SkMII 特异性抑制剂,在肌肉中具有良好的暴露性。 | |||
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]. | |||
T70608 |
cis-Entacapone
|
||
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. | |||
T35236 |
5α-Hydroxy-6-keto cholesterol
YS 64,Yakkasterone,5α-羟基-6-酮胆固醇 |
||
Yakkasterone is a major metabolite of cholesterol formed during exposure of lung epithelial cells to ozone. | |||
T31194 |
Dalapon
Basfapon B,Dowpon M,Dawpon-Rae |
||
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 | |||
T35458 |
(R)-nitro-Blebbistatin
|
||
(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 |
||
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 | |||
T40226 |
FP-Biotin
|
||
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. | |||
T40397 |
3,4,6-Trichlorocatechol
|
||
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. | |||
T37704 |
Olanzapine Lactam Impurity
|
||
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) | |||
T38267 |
Valeryl-L-carnitine (chloride)
Valeryl-L-carnitine (chloride),L-Valerylcarnitine |
||
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] | |||
T26821 |
BIPM
|
||
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 | |||
T61528 |
FGFR-IN-7
|
||
FGFR-IN-7 (compound 17) is an orally active, potent FGFR modulator with the ability to penetrate the blood-brain barrier. It exhibits neuroprotective properties, enhancing brain exposure and decreasing the likelihood of phospholidosis. FGFR-IN-7 proves valuable for research on neurodegenerative diseases [1]. | |||
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。 | |||
TP1179 |
Porcine dynorphin A(1-13)
Dynorphin A Porcine Fragment 1-13 |
||
Porcine dynorphin A (1-13) is a potent, endogenous κ opioid receptor agonist and is antinociceptive at physiological concentrations. Exposure to dynorphin A (1-13) causes acute increases in [Ca2+]i in individual neurons similar to increases seen with acut | |||
T14682 |
BMS-962212
|
Others | Others |
BMS-962212, a direct, reversible, and selective factor XIa (FXIa) inhibitor, demonstrates fast pharmacodynamic (PD) response onset and rapid elimination with a well-tolerated profile. It dependently increases activated partial thromboplastin time and decreases FXI clotting activity exposure [1]. |
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。 | |||
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。 | |||
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。 | |||
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。 | |||
T39836 |
Monoethyl phthalate
|
||
Monoethyl phthalate is a metabolite of diethyl phthalate, serving as a urinary biomarker for phthalate exposure, and indicating potential risks of thyroid cancer and benign nodules. | |||
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
|
||
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 |
||
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
|
||
Tricetin 7-O-glucoside (compound 33)为一种黄酮类单-O-糖苷。 |