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:3870409
已选条件
-
T39713Alogabat;AlogabatAlogabat
Alogabat (example 8) is a positive allosteric modulator (PAM) of the GABA A α5 receptor.
价 格:¥电议型 号:T39713产 地:中国大陆
-
T38858GSK2818713;GSK2818713GSK2818713
GSK2818713 is a novel Hepatitis C NS5A replication complex inhibitor.
价 格:¥电议型 号:T38858产 地:中国大陆
-
T38713Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH;Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OHFmoc-Asn(Ac3AcNH-beta-Glc)-OH|||F
Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH, also known as Fmoc-Asn(Ac3AcNH-beta-Glc)-OH, is a chemical compound used in the synthesis of silicon-fluoride acceptor (SiFA) derivatized octreotate derivatives. SiFA-octreotate analogues, which serve as tumor imaging agents, are valuable tools for positron emission tomography (PET) research.
价 格:¥电议型 号:T38713产 地:中国大陆
-
T37713FunalenoneFunalenoneFunalenone
Funalenone is a phenalenone originally isolated from A. niger. It inhibits HIV-1 integrase (IC50 = 10 μM) and HIV-1 replication in human peripheral blood cells transformed by murine leukemia virus (HPB-M(a); IC50 = 1.7 μM) but is less cytotoxic to mammalian HPB-M(a) cells (IC50 = 87 μM). Funalenone selectively inhibits matrix metalloproteinase-1 (MMP-1; IC50 = 170 μM) over MMP-2 and MMP-9, which it inhibits by 18.3 and 38.2%, respectively, when used at a concentration of 400 μM. It also inhibits
价 格:¥电议型 号:T37713产 地:中国大陆
-
T371385’-O-DMT-N4-Bz-5-Me-dC;5’-O-DMT-N4-Bz-5-Me-dC5’-O-DMT-N4-Bz-5-Me-dC;5’-O-DMT-N4-Bz-5-Me-dC
5’-O-DMT-N4-Bz-5-Me-dC is a modified nucleoside. 5’-O-DMT-2’-O-TBDMS-rI can be used in the synthesis of deoxyribonucleic acid or nucleic acid.
价 格:¥电议型 号:T37138产 地:中国大陆
-
T371375’-O-DMT-N4-Bz-2’-F-dC;5’-O-DMT-N4-Bz-2’-F-dC5’-O-DMT-N4-Bz-2’-F-dC;5’-O-DMT-N4-Bz-2’-F-dC
5’-O-DMT-N4-Bz-2’-F-dC is a nucleoside with protective and modification effects.
价 格:¥电议型 号:T37137产 地:中国大陆
-
T371365’-O-DMT-N4-Ac-2’-F-dC;5’-O-DMT-N4-Ac-2’-F-dC5’-O-DMT-N4-Ac-2’-F-dC;5’-O-DMT-N4-Ac-2’-F-dC
5’-O-DMT-N4-Ac-2’-F-dC is a modified nucleoside and can be used to synthesize DNA or RNA.
价 格:¥电议型 号:T37136产 地:中国大陆
-
T37131MS 15203;MS 15203MS 15203
Potent and selective GPR171 partial agonist (EC50 = 90 nM; 28% inhibition of forskolin activated adenylyl cyclase activity in rat hypothalamic memebranes). Exhibits minimal binding to a panel of ~70 GPCRs and 10 other receptors (<22% of radioligand displaced from the target receptors). Increases neuronal activity in the paraventricular nucleus. Increases food intake and body weight in mice.
价 格:¥电议型 号:T37131产 地:中国大陆
-
T37130MRTX1133 formic;MRTX1133 formicMRTX1133 formic
MRTX1133 is a highly selective, first-in-class inhibitor of KRAS G12D. MRTX1133 targets the KRAS G12D protein in both active and inactive states. MRTX1133 selectively inhibits KRAS G12D mutant, but not KRAS wild-type, tumor cells[1][2].
价 格:¥电议型 号:T37130产 地:中国大陆
-
T3713BAY-876;化合物BAY-876BAY-876
BAY-876 is an orally active and selective inhibitor of glucose transporter 1 (GLUT1, IC50= 2 nM). BAY-876 exhibits >130-fold more selective for GLUT1 than GLUT2, GLUT3, and GLUT4. BAY-876 also inhibits glycolytic metabolism and ovarian cancer growth.
价 格:¥电议型 号:T3713产 地:中国大陆
-
T36713Streptochlorin;StreptochlorinStreptochlorin
Streptochlorin is a bacterial metabolite originally isolated from Streptomyces sp. SF2583 that has diverse biological activities, including antiangiogenic, antiproliferative, and anti-allergic properties. It inhibits TNF-α-induced NF-κB transcriptional activity and decreases proliferation of human umbilical vein endothelial cells (HUVECs) when used at concentrations ranging from 5 to 20 μM. Streptochlorin (12 μg/ml) decreases viability of, as well as induces apoptosis and increases the productio
价 格:¥电议型 号:T36713产 地:中国大陆
-
T35713N-desethyl Brinzolamide (oxalate);N-desethyl Brinzolamide (oxalate)N-desethyl Brinzolamide (oxalate)
N-desethyl Brinzolamide is an active metabolite of the carbonic anhydrase (CA) inhibitor brinzolamide .1It inhibits CAII and CAIV activities (IC50s = 1.28 and 128 nM, respectively).
价 格:¥电议型 号:T35713产 地:中国大陆
-
T35053Vibunazole;化合物 T35053BayN 7133|||Bay-N 7133|||Bay N 7133;BayN 7133|||Bay-N 7133|||Bay N 7133
Vibunazole is an antifungal agent.
价 格:¥电议型 号:T35053产 地:中国大陆
-
T34713Stearyl tyrosine;化合物 T34713Stearyl-tyrosine|||Stearyltyrosine;Stearyl-tyrosine|||Stearyltyrosine
Stearyl tyrosine is an immunoadjuvants, long-chain stearyl ester of amino acids and peptides.
价 格:¥电议型 号:T34713产 地:中国大陆
-
T33713Nomilinic acid glycoside;化合物 T33713Nomilinic acid 17-O-beta-D-glucoside;Nomilinic acid 17-O-beta-D-g
Nomilinic acid glycoside is a limonoid glucoside from the peel of Citrus tangerina.
价 格:¥电议型 号:T33713产 地:中国大陆
-
T32713Levonorgestrel hexanoate;化合物 T32713Plan B;Plan B
Levonorgestrel hexanoate is a manufactured hormone used in a number of birth control methods.
价 格:¥电议型 号:T32713产 地:中国大陆
-
T32000GSK-1071306;化合物 T32000Pazopanib metabolite M27;Pazopanib metabolite M27
GSK-1071306 is a bio-active chemical.
价 格:¥电议型 号:T32000产 地:中国大陆
-
T31402Dexnebivolol;化合物 T31402R67138|||R 67138|||R-67138;R67138|||R 67138|||R-67138
Dexnebivolol ( R67138) is an antagonist of the ?-adrenergic receptor and is an enantiomer of Nebivolol. Nebivolol is a β1 receptor blocker with nitric oxide enhancing vasodilation effect.
价 格:¥电议型 号:T31402产 地:中国大陆
-
T31030CP 71362;化合物 T31030CP71362;CP71362
CP 71362 is a selective pentapeptide renin inhibitor for canine enzymes.
价 格:¥电议型 号:T31030产 地:中国大陆
-
T31026CP 66713;化合物 T31026CP66713|||CP-66713;CP66713|||CP-66713
CP-66713 is an adenosine A2 receptor antagonist.
价 格:¥电议型 号:T31026产 地:中国大陆