找到约 31 条 “Astin C” 相关结果 (用时 0.095 秒)
目录号 | 产品名称 | 中文名称 | 靶点 |
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M2602
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Hydrastinine hydrochloride | Hydrastinine hydrochloride | Others |
Hydrastinine hydrochloride is a semisynthetic alkaloid from the hydrolysis of the alkaloid hydrastine, which was found naturally in small quantities in Hydrastis canadensis L. | |||
M2671
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Epinastine hydrochloride | 依匹斯汀盐酸盐 | Histamine Receptor |
WAL801 hydrochloride | |||
Epinastine HCl是一种抗组胺剂和肥大细胞稳定剂。Epinastine hydrochloride 是一种有效的,选择性的,具有口服活性的组胺 H1 受体 (histamine H1 receptor) 拮抗剂。 | |||
M3487
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Azelastine hydrochloride | 盐酸氮卓斯汀 | Histamine Receptor |
Azelastine HCl是有效的,第二代选择性组胺拮抗剂。 | |||
M7888 | Levocabastine hydrochloride | 左旋多巴 | Others |
Non-peptide histamine H1 receptor antagonist; neurotensin NTS2 receptor ligand. | |||
M14232 | Rapastinel Trifluoroacetate | Rapastinel Trifluoroacetate | GluR |
GLYX-13 Trifluoroacetate | |||
Rapastinel Trifluoroacetate (GLYX-13 Trifluoroacetate) 是一种具有甘氨酸位点部分激动剂性质的 NMDA 受体调节剂。Rapastinel Trifluoroacetate 有潜力用于抑郁症的研究 | |||
M16098 | Murrastinine C | Murrastinine C | Alkaloids |
Murrastinine C | |||
M20495 | Cloperastine hydrochloride | Cloperastine hydrochloride | Histamine Receptor |
HT-11 hydrochloride | |||
Cloperastine is a drug with a central antitussive effect, and is also endowed with an antihistaminic activity. | |||
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. | |||
M43712
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Astin C | Astin C | Others |
Astin C (Asterin) 是一种具有抗癌和抗炎特性的环状五肽。 | |||
M1702
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DCC-2036 | 瑞巴斯替尼 | Src-bcr-Abl |
Rebastinib | |||
DCC-2036 (Rebastinib)是一种Bcr-Abl抑制剂,作用于Abl1(WT)和Abl1(T315I),IC50分别为0.8 nM和4 nM,也抑制SRC, LYN, FGR, HCK, KDR, FLT3,和Tie-2,对c-Kit具有低的抑制活性。 | |||
M2449
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Bepotastine Besilate | 苯磺酸贝托司汀 | Histamine Receptor |
Bepotastine Besilate是一种非镇静作用的,选择性的组胺1 (H1)受体拮抗剂,pIC50为5.7。 | |||
M2679
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Erastin | 铁死亡诱导剂 | Ferroptosis |
Erastin是一种SLC7A11抑制剂,以及ferroptosis激活剂,能通过作用于线粒体VDAC而起作用,选择性作用于携带致癌基因RAS的肿瘤细胞。*该产品在溶液状态不稳定,建议您现配现用 | |||
M2698
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Ferrostatin-1 | 铁抑素-1 | Ferroptosis |
Fer-1 | |||
Ferrostatin-1 (Fer-1)是一种有效的选择性的ferroptosis抑制剂,抑制Erastin诱导的HT-1080细胞铁死亡,EC50为60 nM。 | |||
M3318
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Clemastine Fumarate | 富马酸氯马斯汀 | Histamine Receptor |
Meclastine fumarate | |||
Clemastine Fumarate是一种选择性组胺H1受体拮抗剂,IC50为3 nM。 | |||
M3912
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Vinblastine sulfate | 硫酸长春碱 | Microtubule |
Vincaleukoblastine sulfate salt | |||
Vinblastine sulfate(硫酸长春碱)是一种具有广谱抗肿瘤活性的生物碱,能够抑制细胞内微管的形成和有丝分裂。此外,它还能够抑制nAChR的活性,其IC50值为8.9μM。 | |||
M4551
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Trigonelline hydrochloride | 葫芦巴碱盐酸盐 | Anti-infection |
Trigonelline chloride | |||
Trigonelline hydrochloride 是一种NRF2抑制剂,可阻断血红素和铁代谢相关的NRF2靶基因的表达,与erastin和索拉菲尼协同作用,可促进肝癌细胞的铁死亡。此外,Trigonelline hydrochloride 还能穿透大脑,并可直接结合以及激活肌酸激酶 B(CKB),从而诱导轴突和树突生长。 | |||
M5792
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Mizolastine | 咪唑司汀 | Histamine Receptor |
SL 850324 | |||
Mizolastine 是一种组胺H1受体拮抗剂,IC50为47 nM,用于治疗花粉症(季节性过敏性鼻炎)、荨麻疹和其他过敏性反应。 | |||
M7923 | Myoseverin B | Myoseverin B | Others |
Myoseverin, a new microtubule-binding molecule, acts reversibly on myoblast proliferation without the cytotoxic effects displayed by nonpurine-based microtubule-disrupting molecules, like taxol, vinblastine, nocodazole. | |||
M8311
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MLR-1023 | MLR-1023 | Src-bcr-Abl |
Tolimidone | |||
MLR-1023 (Tolimidone) is a potent, orally active, allosteric activator of the non-receptor Src-related Lyn kinase that produces lasting glucose lowering, reduces HbA1c levels, and preserves pancreatic β-cells in db/db mice. | |||
M8599 | Epiblastin A | Epiblastin A | Others |
Epiblastin A是一种三苯氧胺衍生物,是一种 ATP 竞争性的酪蛋白激酶 1 (CK1) 抑制剂,对 CK1α, CK1δ, 和CK1 ɛ 的 IC50 分别为 8.9, 0.5,和 4.7 µM。此外,Epiblastin A 还能通过抑制 CK1 诱导外胚层干细胞重编程为胚胎干细胞。 | |||
M8613
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CDN1163 | CDN1163 | Others |
CDN1163 is an allosteric activator of sarco/ endoplasmic reticulum Ca2+-ATPase (SERCA) that potently lowered fasting blood glucose, improved glucose tolerance and ameliorated hepatosteatosis in ob/ob mice. | |||
M9172
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Emedastine Difumarate | 富马酸依美斯汀 | Histamine Receptor |
Rapimine | |||
Emedastine Difumarate is a second generation, selective histamine H1 receptor antagonist with anti-allergic activity. | |||
M10244
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Imidazole ketone erastin | Imidazole ketone erastin | Ferroptosis |
Ferroptosis inducer IKE; PUN-30119 | |||
Imidazole ketone erastin (IKE) 是一个ferroptosis铁死亡的诱导剂,它也是一种有效的,选择性的,代谢稳定的system xc–抑制剂。 | |||
M10259
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Spastazoline | 斯巴达唑啉 | Others |
Spastazoline 是一种有效的,选择性aaa+(与多种细胞活动相关的 atpases)蛋白抑制剂,抑制微管切断aaa+蛋白 spastin,它对人spastin的IC50值为99 nM。 | |||
M13991 | Bepotastine | 贝他斯汀;贝托司汀;贝托斯汀;贝他司汀 | Histamine Receptor |
Bepotastine 是一种选择性的具有口服活性的第二代组胺 H1 受体 (histamine H1 receptor) 拮抗剂。Bepotastine 可用于过敏性鼻炎,过敏性结膜炎和荨麻疹/瘙痒症的研究。 | |||
M20452 | Revaprazan Hydrochloride | Revaprazan Hydrochloride | Proton Pump |
YH1885 | |||
Revaprazan Hydrochloride is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. | |||
M20515 | Emedastine | Emedastine | Histamine Receptor |
Emedastine is a potent, high affinity histamine H1-receptor-selective antagonist with Ki of 1.3 ±0.1 nM for H1-receptors while considerably weaker at H2- (K1 = 49,067 ± 11,113 nM) and H3-receptors (Ki = 12,430 ± 1,282 nM). | |||
M21708
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Erastin2 | Erastin2 | Ferroptosis |
Erastin2 是一种ferroptosis铁死亡的诱导剂,是 xc (-) 胱氨酸/谷氨酸转运体系统的有效的选择性抑制剂。 | |||
M28692 | Bezuclastinib | Bezuclastinib | c-Kit |
CGT9486; PLX 9486 | |||
Bezuclastinib (CGT9486; PLX 9486) 是一种有效的 c-kit 和c-kit D816V 抑制剂,0.0001 < IC50 < 1 μM。Bezuclastinib 是一种酪氨酸激酶抑制剂。 | |||
M30621 | Levocabastine | Levocabastine | Histamine Receptor |
R 50547 | |||
Levocabastine (R 50547) 是一种强效选择性组胺 H1 受体拮抗剂。Levocabastine 也是一种选择性、高亲和力的神经降压素受体亚型 2 (NTR2) 拮抗剂,对 mNTR2 的 Ki 值为 17 nM。Levocabastine 可作为 VLA-4 拮抗剂,干扰过敏性结膜炎 (AC) 结膜嗜酸性粒细胞的浸润。 | |||
M38852 | Astin B | Astin B | Apoptosis |
Astin B 是一种口服有效的环状五肽,可从 Aster tataricus 中分离得到。Astin B 在体外和体内均具有肝毒性作用,肝损伤主要由线粒体/半胱天冬酶依赖性方式的细胞凋亡 (apoptosis) 介导。 |