当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型:会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
易推广会员:5年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
企业类型:生产商 【已认证】
注册资金:人民币万 【已认证】
产品数:86101
参观次数:3741461
已选条件
-
T28763Sezolamide hydrochloride;化合物 T28763Sezolamide|||MK-417|||Sezolamide HCl|||MK 417;Sezolamide|||MK-417
Sezolamide hydrochloride is a potent topical carbonic anhydrase inhibitor.
价 格:¥电议型 号:T28763产 地:中国大陆
-
T28743Seglitide acetate;醋酸司格列肽MK 678|||MK678|||MK-678;MK 678|||MK678|||MK-678
Seglitide acetate (MK-678) is a selective agonist of sst2 somatostatin receptor.
价 格:¥电议型 号:T28743产 地:中国大陆
-
T28270Osemozotan HCl;奥莫佐坦MCI-242|||MN-305|||Osemozotan hydrochloride|||MKC-242|||MKC242|||MCI242;MCI-242||
Osemozotan HCl (Osemozotan hydrochloride) is a novel and selective 5-HT1A receptor agonist that reduces methamphetamine-induced c-Fos expression in the medial prefrontal cortex and striatum.Osemozotan HCl is used in the study of mechanical abnormalities of pain and depression.
价 格:¥电议型 号:T28270产 地:中国大陆
-
T28179NMK-TD-100;化合物 T28179NMK-TD 100|||NMK-TD100;NMK-TD 100|||NMK-TD100
NMK-TD-100 is a microtubule modulating agent with anti-proliferative activity by disrupting microtubule functions through tubulin binding. NMK-TD-100 blocks mitosis and induces apoptosis in HeLa cells by binding to tubulin. Polymerization of tissue purified tubulin into microtubules was inhibited by NMK-TD-100 with an IC50 value of 17.5±0.35 ?M.
价 格:¥电议型 号:T28179产 地:中国大陆
-
T28061MK-8876;化合物 T28061MK-8876
MK-8876 is an Inhibitor of HCV NS5B Site D.
价 格:¥电议型 号:T28061产 地:中国大陆
-
T28060MK-8133;化合物 T28060MK-8133
MK-8133 is an antagonist of orexin-2 selective receptor with favorable development properties.
价 格:¥电议型 号:T28060产 地:中国大陆
-
T28059MK-4409;化合物 MK-4409MK4409|||MK 4409;MK4409|||MK 4409
MK-4409 is a novel and selective inhibitor of oxazole fatty acid amide hydrolase FAAH.MK-4409 can be used to study inflammatory and neuropathic pain.
价 格:¥电议型 号:T28059产 地:中国大陆
-
T28058MK-386;化合物 T28058MK 386|||MK386;MK 386|||MK386
MK-386 is a potent and selective inhibitor of human type-1 5alpha-reductase.
价 格:¥电议型 号:T28058产 地:中国大陆
-
T28057MK3577;化合物 T28057MK-3577|||MK 3577;MK-3577|||MK 3577
MK3577 is a glucagon receptor antagonist.
价 格:¥电议型 号:T28057产 地:中国大陆
-
T28056MK319;化合物 T28056MK 319|||MK-319;MK 319|||MK-319
MK319 is an AKR1B10 inhibitor.
价 格:¥电议型 号:T28056产 地:中国大陆
-
T28055MK204;化合物 T28055MK-204|||MK 204;MK-204|||MK 204
MK204 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.
价 格:¥电议型 号:T28055产 地:中国大陆
-
T28054MK181;化合物 T28054MK 181|||MK-181;MK 181|||MK-181
MK181 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.
价 格:¥电议型 号:T28054产 地:中国大陆
-
T28053MK-0736;化合物 T28053MK0736;MK0736
MK-0736 is a potent and selective 11β-HSD-1 inhibitor.
价 格:¥电议型 号:T28053产 地:中国大陆
-
T28052MK-0703;化合物 T28052L-791515|||MK0703|||L791515|||MK 0703|||L 791515;L-791515|||MK0703|||L791515|||MK
MK-0703 is a selective cyclooxygenase-2 inhibitor.
价 格:¥电议型 号:T28052产 地:中国大陆
-
T28051MK 3118;化合物 T28051MK3118|||SCY078|||SCY-078|||MK-3118|||SCY 078;MK3118|||SCY078|||SCY-078|||MK-3118|
MK 3118, a glucan synthase inhibitor, is used potentially for the treatment of candida infection and aspergillosis.
价 格:¥电议型 号:T28051产 地:中国大陆
-
T27749KRP-297;化合物 T27749KRP297|||MK-0767|||L410198|||L 410198;KRP297|||MK-0767|||L410198|||L 410198
KRP297 is a PPAR agonist potentially for the treatment of type 2 diabetes and dyslipidemia.
价 格:¥电议型 号:T27749产 地:中国大陆
-
T27260Emivirine;化合物EmivirineMKC442|||MKC-442|||MKC 442|||DRG-0302|||DRG 0302|||DRG0302;MKC442|||MKC-442|||
Emivirine (MKC-442) is a potent and selective nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1.
价 格:¥电议型 号:T27260产 地:中国大陆
-
T2690Tranilast;曲尼司特MK 341|||SB 252218;曲尼司特|||MK 341|||SB 252218
Tranilast (SB 252218), an antiallergic drug, suppresses lipid mediator and cytokine release from inflammatory cells, therefore utilized in the treatment of allergic disorders.
价 格:¥电议型 号:T2690产 地:中国大陆
-
T26682Atogepant;化合物 T26682MK 8031|||MK8031. Atogepant|||MK-8031;MK 8031|||MK8031. Atogepant|||MK-8031
Atogepant is an antagonist of calcitonin gene-related peptide receptor.
价 格:¥电议型 号:T26682产 地:中国大陆
-
T2650MK-8245;化合物MK-8245MK-8245
MK-8245 is a liver-targeting SCD inhibitor for human SCD1 (IC50: 1 nM) and for rat/mouse SCD1 (IC50: 3 nM), with anti-diabetic and anti-dyslipidemic function.
价 格:¥电议型 号:T2650产 地:中国大陆