找到约 45 条 “SA-VA” 相关结果 (用时 0.297 秒)

目录号 产品名称 中文名称 靶点
M5731 LCZ696 沙库必曲/缬沙坦 Angiotensin Receptor
Sacubitril/Valsartan;Entresto
LCZ696由Valsartan和Sacubitril以1:1的摩尔比组成,是一种首创(first-in-class)的双效血管紧张素受体-脑啡肽酶抑制剂(ARNi,angiotensin receptor-neprilysin inhibitor),用于研究高血压和心脏衰竭。
M9962 Nonivamide 壬酸香草酰胺 TRP Channel
Capsaicin; Pelargonic acid vanillylamide; PAVA
Nonivamide(壬酸香草酰胺)是Capsaicin的类似物,是TRPV1(Vanilloid receptor subtype 1)的激动剂。可以激活TRPV1受体,从而刺激大脑腹侧被盖区的多巴胺能神经元的放电速率,并增加5-羟色胺受体基因HTR2A的表达。
M14988 Chikusetsusaponin Iva 竹节人参皂苷 IVA Others
Calenduloside F
竹节参皂苷ⅣA (Chikusetsusaponin IVa) 是三萜皂苷中主要的活性成,是蛋白激酶的激活剂,对血栓及一些代谢性疾病具有抵抗作用。
M16732 Isosativanone Isosativanone Flavonoids
Isosativanone
M16784 Isosativan Isosativan Flavonoids
Isosativan
M20451 Granisetron Granisetron 5-HT Receptor
Sancuso, Kevatril, Granisetronum, Sustol
Granisetron is a serotonin receptor (5HT-3 selective) antagonist that is used as an antiemetic and antinauseant for cancer chemotherapy.
M20720 Vindesine sulfate Vindesine sulfate Microtubule
Eldesine, Eldisine, Desacetyl Vinblastine amide, Desacetylvinblastine amide, DAVA, DVA, VDS
Vindesine sulfate (Eldesine, Eldisine, Desacetyl Vinblastine amide, Desacetylvinblastine amide, DAVA, DVA, VDS), a vinca alkaloid derived from Catharanthus roseus, is a potent inhibitor of mitosis with antineoplastic activities. Vindesine binds to the microtubular proteins of the mitotic spindle, leading to crystallization of the microtubule and mitotic arrest or cell death.
M21178 TAK-653 TAK-653 GluR
Osavampator
Osavampator (TAK-653) 是一款潜在的同类首创(first-in-class)的α氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)增强剂。
M25409 Satavaptan 沙他普坦;萨塔瓦坦;萨托伐普坦 Vasopressin Receptor
SR121463
Satavaptan(SR 121463)是一种血管加压素V2受体(Vasopressin V2 receptor (V2R))的拮抗剂。Satavaptan能用于对肝硬化腹水的研究。
M25424 Recombinant Human Fibronectin (Oryza sativa) 重组人纤连蛋白 (Oryza sativa) Cytokines and Growth Factors
rhFN
Recombinant Human Fibronectin 重组人纤维连接蛋白是一种细胞外糖蛋白,作为主要的细胞粘附分子之一,纤连蛋白FN在许多重要的生理过程中起着关键性作用,如胚胎生成,伤口愈合,止血和血栓形成。纤连蛋白可以促进细胞生长,提高细胞贴壁率,增强细胞代谢水平,缩短细胞生长时间。
M25438 Recombinant Human Transferrin (Oryza sativa) 重组人转铁蛋白 (Oryza sativa) Cytokines and Growth Factors
转铁蛋白是一种存在于血清中的主要铁结合和细胞传递分子。 无血清细胞培养系统需要一种铁的传递形式。 转铁蛋白是铁的优选传递形式,因为细胞可通过细胞表面上的转铁蛋白受体以生理学上适当的方式对转铁蛋白结合的铁进行处理。
M28943 Sangivamycin Sangivamycin PKC
NSC 65346; BA-90912
Sangivamycin (NSC 65346) 是一种核苷类似物,是蛋白激酶C (PKC) 的有效抑制剂,Ki 为 10 μM。Sangivamycin 对多种人类癌症具有有效的抗增殖活性。
M29474 Azilsartan mopivabil  Azilsartan mopivabil  Angiotensin Receptor
Azilsartan mopivabil 是血管紧张素 II 受体 (angiotensin II receptor) 的强效拮抗剂。
M40501 Salivaricin B Salivaricin B Antibiotic
Salivaricin B是一种由唾液链球菌产生的化合物,并对唾液链球菌、化脓链球菌、轻型链球菌、藤黄微球菌等常见人体微生物具有抑制活性。
M43452 SA-VA SA-VA PROTAC
SA-VA 是一种基于叠氮化物和炔烃的细胞内自组装 PROTAC。
M44441 Sativanone Sativanone Others
Sativanone
M52870 Desamino(D-3-(3′-pyridyl)-Ala2, Arg8)-Vasopressin Desamino(D-3-(3′-pyridyl)-Ala2, Arg8)-Vasopressin Vasopressin Receptor
Desamino(D-3-(3′-pyridyl)-Ala2,Arg8)-Vasopressin 是一种合成的抗利尿激素 (AVP) 的类似物,是抗利尿受体的弱激动剂。
M53219 Sauvagine Sauvagine CRFR
Sauvagine,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。
M56168 Antisauvagine-30 Antisauvagine-30 CRFR
Antisauvagine-30 (aSvg-30) 是一种有效的、竞争性的、选择性的 CRF2 receptor 拮抗剂,针对小鼠 CRF2 细胞和大鼠 CRF1 受体的 Kd 值分别为 1.4 nM 和 153.6 nM。
M56000 Lisavanbulin Lisavanbulin Microtubule
Lisavanbulin (BAL-101553) 是微管蛋白靶向剂 Avanbulin (BAL 27862) 的前药。Lisavanbulin 具有抗肿瘤活性,尤其是在高水平表达末端结合蛋白 1 的肿瘤中。
M55998 Lisavanbulin dihydrochloride Lisavanbulin dihydrochloride Microtubule
Lisavanbulin (BAL-101553) dihydrochloride 是微管蛋白靶向剂 Avanbulin (BAL 27862) 的前体。Lisavanbulin dihydrochloride 具有抗肿瘤活性,尤其是在高水平表达末端结合蛋白 1 的肿瘤中。
M1999 Vadimezan (DMXAA) 伐地美生 STING
ASA404; DMXAA
Vadimezan (DMXAA,ASA-404,伐地美生) 是一种鼠干扰素基因 (STING) 激动剂和 I 型 IFN 及其他细胞因子的强效诱导剂。此外,Vadimezan 还具有抗流感病毒 H1N1-PR8 的活性。
M2475 Bucladesine Sodium Salt 布拉地新钠盐;二丁酰环磷腺甙; PKA
Dibutyryl-cAMP sodium salt; DC2797; Sodium dibutyryl cAMP
Bucladesine Sodium Salt是一种,膜渗透性的选择性PKA激动剂,在PC12细胞中,通过Ca2+-和PKA-依赖的方式激活细胞外信号调节激酶(ERK),显著上调ChAT和VAChT基因表达。
M4446 Cimifugin 升麻素 Others
Cimitin
Cimifugin (Cimitin,升麻素)是Saposhnikovia divaricate 的生物活性成分。Cimifugin 通过调节紧密连接减少上皮衍生的主动关键因子,从而抑制过敏性炎症。
M7243 SAG 21k SAG 21k Others
SAG 21k is a hedgehog signaling activator; brain penetrant and orally bioavailable.
M7698 Capsazepine 辣椒平 TRP Channel
Capsazepine(辣椒平)是一种Capsaicin的合成类似物,是TRPV1(Vanilloid type 1)的拮抗剂,在体外具有抗癌,调节炎症等功能。
M8476 Cuspin-1 Cuspin-1 Others
Cuspin-1 (Chemical Upregulator of SMN Protein-1) is an upregulator of the Survival of Motor Neuron protein (SMN), necessary for survival of motor neurons.
M8772 SAK3 SAK3 Others
SAK3 is a potent and orally active spiroimidazopyridine derivative that enhances Cav3.
M8796 TCPOBOP TCPOBOP Others
TCPOBOP enhances the nuclear receptor CAR transactivation of cytochrome P450 (CYP), as dose-dependent direct agonist of CAR.
M13472 Murepavadin TFA 莫瑞伐定TFA盐 Antibiotic
POL7080 TFA
Murepavadin TFA (POL7080 TFA) 是一种14氨基酸环肽,是一种强效、特异性的抗生素,可用于 Pseudomonas aeruginosa 引起的细菌感染的研究。Murepavadin TFA 靶向作用于脂多糖转运蛋白 portin D。
M14390 Mevalonic acid lithium salt Mevalonic acid lithium salt Metabolite/Endogenous Metabolite
Mevalonic acid lithium salt 是甲羟戊酸途径 (mevalonate pathway) 的前体,对细胞生长和增殖至关重要。
M15075 Ensulizole 苯基苯并咪唑磺酸; 恩索利唑 ROS
PBSA
Ensulizole (PBSA) 是一种水溶性防晒成分,一种磺化的UV吸收剂,其特征是可强烈吸收UVB和部分吸收UVA。Ensulizole 可以在紫外线或阳光照射下通过产生活性氧 (ROS) 来破坏 DNA。
M16158 Koenimbine Koenimbine Alkaloids
NSC 127152; Koenimbin; Kenimbine
Koenimbine is a natural product isolated from Murraya koenigii. The IC50 values of koenimbine in HT-29 and SW48 was calculated to be 50 μg/ml based on the MTT assay. The IC50 value was 75 μg/ml in IEC-18 cells.
M18010 5-hydroxy-3',4',6,7-tetramethoxyflavone 5-羟基-3',4',6,7-四甲氧基黄酮 Antibiotic
5-desmethylsinensetin 可从 Stevia satureiifolia var. satureiifolia 中分离得到,具有抗原生动物的活性。
M18163 Isovitexin 2''-O-arabinoside 异牡荆素-2''-O-阿拉伯糖苷 Others
Isovitexin 2''-O-arabinoside 是 Avena sativa L. 幼苗中的一种非活性类黄酮。
M20400 Morin Hydrate Morin Hydrate Others
Aurantica
Morin hydrate(Aurantica) is a flavonoid isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).
M20453 Mupirocin calcium Mupirocin calcium Antibiotic
pseudomonic acid A
Mupirocin Calcium is the calcium salt form of mupirocin, a natural crotonic acid derivative extracted from Pseudomonas fluorescens,which inhibits bacterial protein synthesis and is used as an antibiotic.
M20467 Paroxetine mesylate Paroxetine mesylate 5-HT Receptor
Paroxetine Mesylate is the mesylate salt form of paroxetine, a phenylpiperidine derivative and a selective serotonin reuptake inhibitor (SSRI) with antidepressant and anxiolytic properties.
M20475 Safinamide Safinamide Others
EMD-1195686, PNU-15774E
Safinamide is an orally active, selective, reversible monoamine oxidase-B inhibitor with both dopaminergic and non-dopaminergic (glutamatergic) properties. The IC50 value of safinamide for MAO-B is 98 nM.
M20606 SAR125844 SAR125844 c-Met
SAR125844 is a potent intravenously active and highly selective MET kinase inhibitor, displaying nanomolar activity against the wild-type kinase (IC50 value of 4.2 nmol/L) and H1094Y, Y1235D, M1250T, L1195V, and D1228H kinase domain mutants (IC50 values of 0.22, 1.7, 6.5, 65, and 81 nmol/L, respectively).
M20614 NSC-87877 disodium salt NSC-87877 disodium salt Phosphatase
NSC-87877 disodium is a cell-permeable inhibitor of both SHP-1 and SHP-2 with IC50 values of 355 and 318 nM respectively. NSC-87877 disodium salt also inhibits EGF-induced Erk1/2 activation in HEK293 cells and significantly reduces MDA-MB-468 cell viability/proliferation.
M20914 Isosorbide dinitrate Isosorbide dinitrate Others
Sorbide nitrate, Sorbidnitrate, Isordil, Nitrosorbide
Isosorbide Dinitrate is the dinitrate salt form of isosorbide, an organic nitrate with vasodilator activity. It is used in the treatment of angina pectoris.
M20927 Betahistine mesylate Betahistine mesylate Histamine Receptor
Betahistine mesylate is the mesylate salt form of Betahistine, a histamine analog and H3 receptor agonist that serves as a vasodilator.
M20937 Midodrine hydrochloride Midodrine hydrochloride Adrenergic Receptor
Midodrine hydrochloride is the hydrochloride salt form of midodrine, an adrenergic alpha-1 agonist used as a vasopressor.
M20942 Choline Fenofibrate Choline Fenofibrate PPAR
Choline fenofibrate is a newly developed choline salt of fenofibric acid, a synthetic phenoxy-isobutyric acid derivate with antihyperlipidemic activity that acts as an PPARα agonist.








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