65
25
3
10
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T9048 |
Ecamsule
|
Others | Others |
Ecamsule 是一种亚苄基樟脑衍生物,其中许多以其出色的光稳定性而闻名。 可添加到防晒霜中以过滤掉 UVA 射线。 | |||
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。 | |||
T7769 |
Nonapeptide-1
Met-Pro-D-Phe-Arg-D-Trp-Phe-Lys-Pro-Val-,九胜肽-1,Melanostatine™ 5 |
Others | Others |
Nonapeptide-1 (Melanostatine™ 5) 可以抑制黑色素的合成,这使得它对治疗某些皮肤病很感兴趣。 | |||
T77695 |
Muvalaplin
LY3473329 |
Others | Others |
Muvalaplin (LY3473329) 是一种具有口服活性的脂蛋白 (a) Lp (a) 抑制剂,可阻断 apo(a)-apo B100 相互作用来抑制 Lp(a) 的形成。 | |||
T1487 |
Fluvastatin sodium
XU 62320 sodium,XU-62-320,氟伐他汀钠,Fluvastatin sodium salt |
Ferroptosis; HMG-CoA Reductase; Autophagy | Apoptosis; Autophagy; Metabolism |
Fluvastatin sodium (Fluvastatin sodium salt) salt 是羟甲基戊二酰辅酶 A 还原酶的竞争性抑制剂,IC50为 8 nM。它通过依赖 Nrf2 的抗氧化通路保护血管平滑肌细胞免受氧化应激,是一种常用的降胆固醇剂。 | |||
T12652 |
(Rac)-5-Keto Fluvastatin
5-Ketofluvastatin,3-Hydroxy-5-Keto Fluvastatin,rac 5-Keto Fluvastatin |
Others | Others |
(Rac)-5-Keto Fluvastatin (rac 5-Keto Fluvastatin) 是 Fluvastatin 的杂质,Fluvastatin 是一种 HMG-CoA 还原酶的抑制剂。 | |||
T21405 |
Fluvastatin
Canef,XU-62320,Vastin,Cranoc,Lescol |
HMG-CoA Reductase | Metabolism |
Fluvastatin (XU-62320) 是一种具有高效性和竞争性的 HMG-CoA 还原酶抑制剂(IC50 :8 nM),可通过依赖 Nrf2 通路抑制血管平滑肌细胞免受氧化应激,用于降低血浆胆固醇水平和预防心血管疾病。 | |||
T38863 |
Luvadaxistat
TAK-831,NBI 1065844 |
Others | Others |
Luvadaxistat (TAK-831) 是一种具有口服活性、高效性和高选择性的 D-氨基酸氧化酶 (DAAO) 抑制剂,对 D-丝氨酸的氧化脱氨的 IC50 值为 14 nM。Luvadaxistat 可用于研究精神分裂和认知障碍。 | |||
T1510 |
Rosuvastatin calcium
ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium,瑞舒伐他汀钙 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin calcium (ZD4522) 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 | |||
T11684 |
Isoguvacine hydrochloride
1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride,异四氢烟酸 |
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Isoguvacine hydrochloride (1,2,3,6-tetrahydro-4-pyridinecarboxylic acid hydrochloride) 是 GABA 受体激动剂。它与大鼠突触皮质膜结合并激活 α1β2γ2S、α2β2γ2S、α3β2γ2S、α5β2γ2S 和 ρ1 亚基 GABAA 受体。 | |||
T2516 |
Amuvatinib
MP470,HPK 56 |
Apoptosis; FLT; c-Met/HGFR; c-RET; DNA/RNA Synthesis; PDGFR; c-Kit | Angiogenesis; Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; Tyrosine Kinase/Adaptors |
Amuvatinib (MP470) 是一种多靶点酪氨酸激酶抑制剂,对突变 c-Kit,PDGFRα,Flt3,c-Met 和 c-Ret 具有活性。它还是一种 DNA 修复抑制剂,靶向蛋白 DNA 修复 RAD51,从而破坏 DNA 损伤修复,具有抗肿瘤活性。 | |||
T68018 |
Tuvatexib
|
VDAC | Membrane transporter/Ion channel |
Tuvatexib 是一种小分子VDAC/HK2双调节剂。 | |||
T1676 |
Rosuvastatin
罗伐他汀,ZD 4522,瑞舒伐他汀 |
Potassium Channel; HMG-CoA Reductase; Autophagy | Autophagy; Membrane transporter/Ion channel; Metabolism |
Rosuvastatin (ZD 4522) 是一种抗血脂药,可竞争性抑制羟甲基戊二酰辅酶 A 还原酶,用于降低血浆胆固醇水平和预防心血管疾病。它降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go 相关基因电流,IC50为 195 nM,延迟心脏复极化,延长动作电位持续时间和校正 QT 间期间隔。 | |||
T10126 |
(3R,5R)-Rosuvastatin
|
Others | Others |
(3R,5R)-Rosuvastatin is the (3R,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoA reductase inhibitor (IC50: 11 nM). | |||
T80060 |
Pyruvate carboxylase
|
Endogenous Metabolite | Metabolism |
Pyruvate carboxylase是一种催化反应中丙酮酸与HCO3−和MgATP进行依赖性羧化生成草酰乙酸的含生物素酶。它在调控肝脏糖异生、脂肪细胞脂肪酸合成及胰腺β细胞胰岛素分泌方面,对全身能量平衡发挥关键作用。 | |||
TP2121 |
Sauvagine
|
||
Corticotropin-releasing factor (CRF) receptor agonist. Ki values are 9.4, 9.9, and 3.8 nM for inhibition of 125I-[D-Tyr1]astressin binding to hCRF-R1, rCRF-R2a and mCRF-R2b respectively. | |||
T10129 |
(3S,5R)-Fluvastatin sodium
(3S,5R)-XU 62-320 |
Others | Others |
(3S,5R)-Fluvastatin sodium is the (3S,5R)-enantiomer of Fluvastatin. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). Fluvastatin protects vascular smooth muscle cells against oxidative stress through the Nrf2- | |||
T34325 |
Ribuvaptan
|
Others | Others |
Ribuvaptan is a antagonist of vasopressin receptor . | |||
T125971 |
Isotriuvaretin
|
Others | Others |
Isotriuvaretin 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T125971,CAS号为 137397-72-9。 | |||
T60341 |
Pyruvate Carboxylase-IN-1
|
Others | Others |
Pyruvate Carboxylase-IN-1 (compound 37) 是一种有效的丙酮酸羧化酶(PC) 抑制剂,对于基于细胞裂解物和基于细胞的 PC 活性,IC50s 分别为 0.204 和 0.104 μM。Pyruvate Carboxylase-IN-1 是毛兰素的天然类似物。Pyruvate Carboxylase-IN-1 抑制 PC 的酶活性,介导人肝细胞癌 (HCC) 的抗癌作用。 | |||
T78351 |
Phosphoenolpyruvate carboxylase
PEPC |
Others | Others |
Phosphoenolpyruvate carboxylase (PEPC) 是将磷酸烯醇丙酮酸同碳酸氢盐在 Mg2+ 存在下以不可逆的过程转变成草酰乙酸和无机磷的二氧化碳固定酶。该酶在催化景天酸代谢植物中二氧化碳(CO(2))的初级同化过程中发挥关键作用,并在植物代谢的昼夜模式设定中扮演主要角色。 | |||
T81257 |
Rosuvastatin zinc salt
Rosuvastatin zinc |
Others | Others |
Rosuvastatin zinc salt (Rosuvastatin zinc),为Rosuvastatin的含锌盐形态,属于HMG-CoA还原酶抑制剂类药物,常用于动脉粥样硬化的研究领域。 | |||
T84962 |
(3R,5R)-Rosuvastatin calcium
|
Others | Others |
(3R,5R)-Rosuvastatin, a potential impurity detected in bulk rosuvastatin formulations, arises as a degradation product through various stresses including acid or base hydrolysis, thermal, photolytic, hydrolytic, oxidative stress, or during storage. This compound is associated with the HMG-CoA reductase inhibitor class to which rosuvastatin belongs. | |||
T75894 |
Sauvagine TFA
|
||
Sauvagine TFA,是一种来自青蛙皮肤的 40 个氨基酸的神经肽,是哺乳动物 CRF 激动剂。Sauvagine TFA 可有效从大鼠垂体细胞释放 ACTH。Sauvagine TFA 在利尿,心血管系统和内分泌腺体方面具有许多药理作用。 | |||
T62125 |
Colistin adjuvant-1
|
Others | Others |
Colistin adjuvant-1 是一种粘菌素佐剂 (colistin adjuvant),对革兰氏阴性细菌具有增强的粘菌素增强活性。Colistin adjuvant-1 对 NF-κB 表现出抑制作用 (IC50: 0.209 μM)。 | |||
T76143 |
Pyruvate oxidase
|
Others | Others |
Pyruvate oxidase(PoxB) 是一种焦磷酸硫胺素依赖型的氧化酶,可以催化丙酮酸氧化脱羧生成乙酰磷酸、二氧化碳和水。Pyruvate oxidase 是细菌代谢中的一种重要酶,常用于生化研究。 | |||
T124547 |
Diuvaretin
|
Others | Others |
Diuvaretin 是一种有用的有机化合物,可用于生命科学领域的相关研究。其产品编号为 T124547,CAS号为 61463-04-5。 | |||
T124682 |
Uvamalol D
|
Others | Others |
Uvamalol D 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T124682。 | |||
T69237 |
Phosphoenol-3-bromopyruvate
|
Others | Others |
Phosphoenol-3-bromopyruvate is a mechanism-based inhibitor of phosphoenolpyruvate carboxylase from maize | |||
T125561 |
Uvarigranol E
|
Others | Others |
Uvarigranol E 是一种有用的有机化合物,可用于生命科学领域的相关研究,其产品编号为 T125561。 | |||
T69178 |
Rosuvastatin lactone
|
Others | Others |
Rosuvastatin lactone is the lactone form of the HMG-CoA reductase inhibitor rosuvastatin. It is found in vivo following rosuvastatin administration. Rosuvastatin lactone is an inhibitor of the cytochrome P450 (CYP) isoforms CYP2C9.1 and CYP2C9.3 (IC50s = 8.52 and 4.1 µM, respectively). | |||
T61154 |
Colistin adjuvant-2
|
Others | Others |
Colistin adjuvant-2 is a compound that acts as a potentiation agent for colistin, effectively enhancing its activity against Gram-negative bacteria [1]. | |||
T63430 |
Rosuvastatin Sodium
|
Others | Others |
Rosuvastatin Sodium 是竞争性HMG-CoA 还原酶 (HMGCR) 抑制剂 (IC50: 11 nM),能够有效阻断hERG 电流 (IC50: 195 nM)。Rosuvastatin Sodium 可以有效减少低密度脂蛋白 (LDL) 胆固醇,甘油三酯和 C- 反应蛋白水平。Rosuvastatin Sodium 能够减少成熟 hERG 的表达,并抑制及热休克蛋白 70 (Hsp70) 与 hERG 蛋白的相互作用。 | |||
T77187 | Zeluvalimab | ||
Zeluvalimab (AMG-404) 是一种靶向PD-1受体的单克隆抗体,可用于癌症的研究。 | |||
T10131 |
(3S,5R)-Rosuvastatin
|
Others | Others |
(3S,5R)-Rosuvastatin is the (3R,5R)-enantiomer of Rosuvastatin. Rosuvastatin is a competitive HMG-CoA reductase inhibitor (IC50: 11 nM). | |||
TP2091 |
Antisauvagine-30
|
||
Potent, selective and competitive corticotropin-releasing factor CRF2 receptor antagonist (Kd values are 1.4 and 153.6 nM for binding to mouse CRF2β and rat CRF1 receptors respectively). Inhibits sauvagine-stimulated cAMP accumulation in HEK-mCRF2β cells | |||
T80559 |
Duvakitug
|
||
Duvakitug为针对TNFSF15/TL1A的人源IgG1-λ2型单克隆抗体,在CHOK1SV细胞系的内源性谷氨酰胺合成酶(GS)阳性细胞中表达,适用于克罗恩病(Crohn's Disease, CD)研究。 | |||
T19132 |
(3R,5R)-Rosuvastatin Lactone
|
Others | Others |
(3R,5R)-Rosuvastatin Lactone is an isomer of Rosuvastatin Lactone. | |||
T10338 |
Antisauvagine-30 TFA (220673-95-0 free base)
Antisauvagine-30 TFA,aSvg-30 TFA |
Others | Others |
Antisauvagine-30 TFA (aSvg-30 TFA) is a highly selective and competitive antagonist of CRF2 receptor peptidic. It shows a Kd of 1.4 nM and 150 nM for mCRFR2β and CRFR1, respectively. | |||
T39036 |
(3R,5S)-Fluvastatin
(3R,5S)-Fluvastatin,(3R,5S)-XU 62-320 free acid |
Others | Others |
(3R,5S)-Fluvastatin, the 3R,5S-isomer of Fluvastatin (XU 62-320 free acid), stands as the inaugural fully synthetic, competitive inhibitor of HMG-CoA reductase, exhibiting an IC50 value of 8 nM. It safeguards vascular smooth muscle cells from oxidative stress by activating the Nrf2-dependent antioxidant pathway. | |||
TP2121L |
Sauvagine acetate(74434-59-6 Free base)
|
||
Sauvagine acetate(74434-59-6 Free base) 是一种促肾上腺皮质激素释放因子 (CRF) 受体激动剂。 抑制 125I-[D-Tyr1]astressin 与 hCRF-R1、rCRF-R2a 和 mCRF-R2b 结合的 Ki 值分别为 9.4、9.9 和 3.8 nM。 | |||
T70592 |
Makaluvamine A
|
Others | Others |
Makaluvamine A comes from the fruiting bodies of Didymium bahiense that act as active anti-cancer agents and DNA topo II inhibitors. | |||
T76115 |
Pyruvate kinase
|
Others | Others |
Pyruvate kinase 是一种糖酵解酶,催化磷酸烯醇式丙酮酸和 ADP 转化为丙酮酸和 ATP。 | |||
T34266 |
Rauvanine
Rauvanin |
Others | Others |
Rauvanine a alkaloid of Rauwolfia vomitora. | |||
T68381 |
Tuvatidine
|
Others | Others |
Tuvatidine is a histamine 2 receptor antagonist. | |||
T39611 |
Enuvaptan
Enuvaptan,BAY-2327949 |
Others | Others |
Enuvaptan is a vasopressin receptor antagonist and has the potential for research into renal and cardiovascular diseases. | |||
T61961 |
Pyruvate Carboxylase-IN-2
|
Others | Others |
Pyruvate Carboxylase-IN-2 是毛兰素的天然类似物。Pyruvate Carboxylase-IN-2 (compound 29) 是有效的丙酮酸羧化酶(pyruvate carboxylase) 抑制剂。在基于细胞裂解物和基于细胞的 PC 活性中,Pyruvate Carboxylase-IN-2的 IC50s 分别为 0.065 和 0.097 μM。Pyruvate Carboxylase-IN-2介导人肝细胞癌 (HCC) 的抗癌作用。 | |||
T14282 |
Amuvatinib hydrochloride
HPK 56 hydrochloride,MP470 hydrochloride |
Others | Others |
Amuvatinib hydrochloride (MP470 hydrochloride) is an orally bioavailable multi-targeted tyrosine kinase inhibitor with potent activity against mutant c-Kit, PDGFRα, Flt3, c-Met and c-Ret and is also a DNA repair suppressor through suppression of DNA repai | |||
T35419 |
τ-Fluvalinate
|
Others | Others |
τ-Fluvalinate is a pyrethroid acaricide.1It induces tail currents in Western honeybee (A. mellifera) voltage-gated sodium channels (AmNav1) expressed inXenopusoocytes (EC50= 60 nM). It also induces tail currents in honeybee parasitic Varroa mite (V. destructor) Nav1 channels (VdNav1) expressed inXenopusoocytes (EC50= 160 nM) with a faster tail current decay than that of AmNav1 channels. Topical application of τ-fluvalinate (2 μl) in combination with coumaphos , atrazine , 2,4-DMPF, chlorpyrifos ... | |||
T35718 |
N-desmethyl Rosuvastatin (sodium salt hydrate)
|
Others | Others |
N-desmethyl Rosuvastatin is an active metabolite of the HMG-CoA reductase inhibitor rosuvastatin .1,2N-desmethyl Rosuvastatin is formed when rosuvastatin undergoes demethylation, primarily by the cytochrome P450 (CYP) isoform CYP2C9 and to a lesser extent by CYP2C19 and CYP3A4.1 1.Macwan, J.S., Ionita, I.A., and Akhlaghi, F.A simple assay for the simultaneous determination of rosuvastatin acid, rosuvastatin-5S-lactone, and N-desmethyl rosuvastatin in human plasma using liquid chromatography-tand... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T0473 |
Arbutin
Uva,p-Arbutin,p-Arbutin,熊果苷,β-Arbutin |
Tyrosinase | Proteases/Proteasome |
Arbutin (p-Arbutin) 是一种从熊果植物 Arctostaphylos uvaursi 中分离出的天然多酚,具有抗氧化,抗炎和抗肿瘤特性。它是一种脱色剂,也是一种黑色素细胞中酪氨酸酶的竞争性抑制剂,对单酚酶的 Kiapp 值为 1.42 mM;对二酚酶Kiapp 的值为 0.9 mM。 | |||
T7557 |
Guvacine hydrochloride
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Guvacine hydrochloride 是从槟榔中得到的一种生物碱,是 GABA 摄取抑制剂,IC50为 10 μM。它对几种克隆的 GABA 转运体具有适度的选择性。 | |||
T8030 |
Ethyl pyruvate
|
Apoptosis; Antioxidant | Apoptosis; oxidation-reduction |
Ethyl pyruvate 是一种内源性代谢物丙酮酸的衍生物,是一种抗炎剂。 | |||
T4891 |
Sodium phenylpyruvate
苯丙酮酸钠,Phenylpyruvic acid, sodium salt |
Others | Others |
Sodium phenylpyruvate (Phenylpyruvic acid, sodium salt) 是phenylpyruvate decarboxylase 和phenylpyruvate tautomerase 互变异构酶的底物。 | |||
TN2290 |
Uvaol
|
Endogenous Metabolite; JNK; PPAR | DNA Damage/DNA Repair; MAPK; Metabolism |
Uvaol 存在于橄榄和初榨橄榄油中,具有抗炎、抗增殖和血管舒张活性。 | |||
T5805 |
Guvacoline hydrochloride
1,2,5,6-四氢吡啶-3-甲酸甲酯盐酸盐,Norarecoline hydrochloride,去甲槟榔碱 |
AChR | Neuroscience |
Guvacoline hydrochloride (Norarecoline hydrochloride) 是从三药槟榔中发现的一种吡啶生物碱,可作为心房和回肠的毒蕈碱激动剂。 | |||
TJS0123 |
Guvacine ethyl ester
槟榔碱,PT00442-2 |
Others | Others |
Guvacine ethyl ester (Arecoline) 是一种生物碱,存在于槟榔中,可用于 GABA 摄取抑制剂的合成。 | |||
TN1717 |
Guvacine
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Guvacine can enhance the inhibition of spinal neurones by GABA. | |||
T32326 |
Juvabione
|
||
Juvabione is the methyl ester of todomatuic acid, both of which are sesquiterpenes (C15) found in the wood of true firs of the genus Abies. They exist as part of a mixture of sesquiterpenes based on the bisabolane scaffold. Sesquiterpenes of this family, | |||
T13956 |
Uvarigrin
|
Others | Others |
Uvarigrin induces tumor multidrug resistance cell apoptosis and triggers Caspase-9 activation. Uvarigrin is isolated from the roots of Uvaria calamistrata. | |||
T40665 |
Uvaretin
|
Others | Others |
Uvaretin demonstrates potent antibacterial activity against B. subtilis (EC50: 8.7 μM) and S. epidermidis (IC50: 7.9 μM). | |||
T80887 |
Uvaol diacetate
|
||
Uvaol diacetate (Compound 5),一种从Nerium oleander L.叶提取的三萜化合物。 | |||
TN2292 |
Uvarigranol C
|
Others | Others |
Uvarigranol C is a natural product | |||
TN4465 |
Luvangetin
|
COX; Prostaglandin Receptor; Antifection | GPCR/G Protein; Immunology/Inflammation; Microbiology/Virology; Neuroscience |
Luvangetin may have anti-inflammatory activity, it can inhibit NO and PGE2 production in LPS-stimulated BV2 cells. Luvangetin shows significant protection against pylorus-ligated and aspirin-induced gastric ulcers in rats and cold restraint stress-induced | |||
TN6381 |
Grandiuvarin A
|
||
Grandiuvarin A 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN6381,CAS号为 882692-93-5。 | |||
T80014 |
Guvacine hydrobromide
|
GABA Receptor | Membrane transporter/Ion channel; Neuroscience |
Guvacine hydrobromide为槟榔中提取的生物碱,具有作为GABA摄取抑制剂的活性。该化合物对大鼠GAT-1、GAT-2和GAT-3的GABA摄取抑制作用具有不同的IC50值,分别为39 μM、58 μM及378 μM。 | |||
TN3824 |
Demethylluvangetin
|
Others | Others |
Demethylluvangetin 是一种天然产物,可用于生命科学领域的相关研究。其产品编号为 TN3824,CAS号为 64652-10-4。 | |||
TN2291 |
Uvarigranol B
|
Others | Others |
Uvarigranol B is a natural product | |||
T40695 |
Isouvaretin
|
Others | Others |
Isouvaretin demonstrates potent antibacterial activity against B. subtilis and S. epidermidis. | |||
T80886 |
Uvariol
21-Hydroxylanosterol |
Others | Others |
Uvariol (21-Hydroxylanosterol)为一自Piptostigma fugax根部提取得到的天然化合物。 | |||
TN7117 |
regaloside I
|
Others | Others |
Regaloside I 是百合中的单体成分,可能是保护人类皮肤成纤维细胞免受 UVA 诱导的形态变化的主要成分。 | |||
TN6988 |
Pterine-6-carboxylic acid
6-Carboxypterin |
DNA; PDE | DNA Damage/DNA Repair; Metabolism |
Pterine-6-carboxylic acid (6-Carboxypterin) 是叶酸的光降解产物,可被用作光敏感剂研究UVA 破环DNA 结构的分子机制。 | |||
TN1060 |
Ganoderol A
灵芝醇 A,灵芝醇A |
Others | Others |
Ganoderol A has significant anti-inflammatory activity and protection against UVA damage. it has an inhibitory effect on angiotensin converting enzyme activity and cholesterol biosynthesis. | |||
TN1542 |
Cycloheterophyllin
|
NADPH-oxidase; PKA; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Immunology/Inflammation; Tyrosine Kinase/Adaptors |
Cycloheterophyllin has an antioxidant effect, it is a photoprotective agent that inhibits ultraviolet A (UVA)-induced oxidative stress and damage, and could be used in the research on and prevention of skin photoaging. | |||
T80654 |
3,3′-Bisdemethylpinoresinol
|
MMP | Proteases/Proteasome |
3,3′-Bisdemethylpinoresinol,一种木质素类的天然产物,具有抑制UVA照射下人真皮成纤维细胞中MMP-1的活性。该化合物可从Morinda citrifolia种子中分离提取。 |
Cat. No. | Product Name | Species | Expression System |
---|---|---|---|
TMPH-00637 |
RuvA Protein, E. coli, Recombinant (His & SUMO)
ruvA,Holliday junction branch migration complex sub... |
E. coli | E. coli |
RuvA Protein, E. coli, Recombinant (His & SUMO) is expressed in E. coli expression system with N-6xHis-SUMO tag. The predicted molecular weight is 38.1 kDa and the accession number is P0A809. | |||
TMPJ-00457 |
OGG1 Protein, Human, Recombinant
OGH1,N-Glycosylase/DNA Lyase,DNA-(Apurinic or Apyrimidinic S... |
Human | E. coli |
Human N-Glycosylase/DNA Lyase(OOG1) is a DNA repair enzyme, which belongs to the type-1 OGG1 family. OOG1 incises DNA at 8-oxoG residues, and excises 7,8-dihydro-8-oxoguanine and 2,6-diamino-4-hydroxy-5-N-methylformamidopyrimidine (FAPY) from damage DNA. It has a β-lyase activity that nicks DNA 3’ to the lesion. OOG1 together with APEX1 is recruited to nuclear speckles in UVA-irradiated cells. The OGG1 gene mutations may be caused Renal cell carcinoma. | |||
TMPJ-00817 |
HO-1 Protein, Human, Recombinant
HO,HMOX1,HO-1,Heme Oxygenase 1,HO1 |
Human | E. coli |
Heme Oxygenase 1 (HO-1) is an enzyme in endoplasmic reticulum that belongs to the heme oxygenase family. HO-1 cleaves the heme ring at the alpha methene bridge to form Biliverdin. Biliverdin is subsequently converted to Bilirubin by Biliverdin reductase. In physiological state, the highest activity of HO-1 is found in the spleen, where senescent erythrocytes are sequestrated and destroyed. HO-1 activity is highly inducible by its substrate heme and by various non-heme substances such as heavy me... |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12759 |
Rosuvastatin D6 Sodium
|
Others | Others |
Rosuvastatin D6 Sodium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T10128 |
(3S,5R)-Fluvastatin D6 sodium
(3S,5R)-XU 62-320 D6 |
Others | Others |
(3S,5R)-Fluvastatin D6 sodium is the deuterium-labeled (3S,5R)-Fluvastatin sodium. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). | |||
TMIH-0052 |
3S,5R-Fluvastatin-d6
|
||
3S,5R-Fluvastatin-d6 是 3S,5R-Fluvastatin 的氘代化合物。3S,5R-Fluvastatin 的 CAS 号为 94061-81-1。 | |||
T11306 |
Fluvastatin D6 sodium
XU 62-320 (D6) |
Others | Others |
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium. | |||
T19551 |
Rosuvastatin D6 Calcium
|
Others | Others |
Rosuvastatin D6 Calcium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T12757 |
Rosuvastatin D3 Sodium
|
Others | Others |
Rosuvastatin D3 Sodium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
TMIH-0242 |
Fluvastatin-d6 Sodium Salt
|
||
Fluvastatin-d6 Sodium Salt 是 Fluvastatin Sodium Salt 的氘代化合物。Fluvastatin Sodium Salt 的 CAS 号为 93957-55-2。Fluvastatin sodium salt 是羟甲基戊二酰辅酶 A 还原酶的竞争性抑制剂,IC50为 8 nM。它通过依赖 Nrf2 的抗氧化通路保护血管平滑肌细胞免受氧化应激,是一种常用的降胆固醇剂。 | |||
TMIJ-0164 |
Rosuvastatin-d6 Sodium Salt
|
||
Rosuvastatin-d6 Sodium Salt 是 Rosuvastatin Sodium Salt 的氘代化合物。Rosuvastatin Sodium Salt 的 CAS 号为 1007871-86-4。 | |||
TMIH-0505 |
Rosuvastatin-d3 intermediate
|
||
Rosuvastatin-d3 intermediate 是 Rosuvastatin intermediate 的氘代化合物。 | |||
TMIH-0504 |
Rosuvastatin-d6 Calcium Salt
|
||
Rosuvastatin-d6 Calcium Salt 是 Rosuvastatin Calcium Salt 的氘代化合物。Rosuvastatin Calcium Salt 的 CAS 号为 147098-20-2。Rosuvastatin calcium 是肝羟甲基戊二酰辅酶 A 还原酶的选择性和竞争性抑制剂,具有抗血脂活性。它降低成熟 hERG 的表达以及热休克蛋白 70 与 hERG 蛋白的相互作用,还降低低密度脂蛋白胆固醇、甘油三酯和 C-反应蛋白水平。它阻断人类醚-a-go-go相关基因电流,延迟心脏复极化,来延长动作电位持续时间和校正 QT 间期间隔。 |