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T10893CS-722 Free baseCS722 Free base,CS 722 Free base
CS-722 Free base is a synthetic central muscle relaxant with muscle relaxant activity and inhibitory effect on spinal reflex. CS-722 Free base may inhibit spontaneous inhibitory post-synaptic current and excitatory post-synaptic current in hippocampal culture by inhibiting sodium current and calcium current.
价 格:¥电议型 号:T10893产 地:中国大陆
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T19814CP-3807366,7-二甲氧乙氧基喹唑啉-4-酮;CP380736;CP 380736;PF-00520893;PF00520893;PF 00520893
CP-380736 is an epidermal growth factor receptor (EGFR) inhibitor. EGFR is a tyrosine kinase that activates MAPK, JNK, and Akt pathways, and is an important mediator of several types of cancer.
价 格:¥电议型 号:T19814产 地:中国大陆
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T0893Tinidazole替硝唑;CP12574
Tinidazolea is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole´s
价 格:¥电议型 号:T0893产 地:中国大陆
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T0893TinidazoleTinidazole,CP12574,
Tinidazolea is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole´s
价 格:¥电议型 号:T0893产 地:美洲
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T12055MK 0893MK 0893
MK 0893 is a potent, selective antagonist of glucagon receptor.
价 格:¥电议型 号:T12055产 地:美洲
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T80893Urease-IN-9;化合物 Urease-IN-9Urease-IN-9
Urease-IN-9 (Compound 1e), an urease inhibitor with an IC50 of 19.5 μM, effectively impedes the enzyme´s activity [1].
价 格:¥电议型 号:T80893产 地:中国大陆
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T70893K811;化合物 K811K811
K811 is an ASK1-specific inhibitor that prolongs survival in a mouse model of amyotrophic lateral sclerosis. K811 efficiently prevented cell proliferation in cell lines with high ASK1 expression and in HER2-overexpressing GC cells. Treatment with K811 reduced sizes of xenograft tumors by downregulating proliferation markers.
价 格:¥电议型 号:T70893产 地:中国大陆
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T60893Ep vinyl quinidine;化合物 Ep vinyl quinidineEp vinyl quinidine
Ep vinyl quinidine (3-Epiquinine) is an epi-vinyl stereoisomer of Quinidine. Quinidine can be used in malaria research which is also an antiarrhythmic agent. Quinidine is a potent, orally active, selective inhibitor of cytochrome P450db as well as a blocker of K+ channel with an IC 50 of 19.9 μM [1] [2] [3].
价 格:¥电议型 号:T60893产 地:中国大陆
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T40893Estrogen receptor modulator 6;Estrogen receptor modulator 6Estrogen receptor modulator 6
Estrogen receptor modulator 6 (compound 3a) is a highly specific and potent agonist of the estrogen receptor (ER) β with a remarkable affinity (K i = 0.44 nM). This compound exhibits an impressive 19-fold selectivity for ERβ over ERα, as evidenced by its affinity (K i = 8.4 nM).
价 格:¥电议型 号:T40893产 地:中国大陆
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T30893Chlorfenprop-methyl;化合物 T30893BAY 70533|||W5769|||Bayer 70533|||W 5769|||W-5769;BAY 70533|||W5769|||
Chlorfenprop-methyl is a biochemical.
价 格:¥电议型 号:T30893产 地:中国大陆
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T30538BMS-695735;化合物 T30538CHEMBL459729|||DNC008930|||BMS 695735|||BMS695735|||BDBM27888;CHEMBL459729|||DN
BMS-695735, a benzimidazole inhibitor of insulin-like growth factor-1 receptor, has broad-spectrum antitumor activity in vivo. It was found that BMS-695735 had strong inhibition of CYP3A4, induction of CYP3A4 mediated by PXR transactivation, poor water solubility, and high plasma protein binding.
价 格:¥电议型 号:T30538产 地:中国大陆
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T20893PEG17;化合物 T20893PEG17
PEG17 is a PEG linker, which may be useful in the development of antibody-drug conjugates.
价 格:¥电议型 号:T20893产 地:中国大陆
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T19814CP-380736;6,7-二甲氧乙氧基喹唑啉-4-酮PF 00520893|||CP380736|||PF00520893|||CP 380736|||PF-00520893;PF 00520893
CP-380736 (PF-00520893) is an epidermal growth factor receptor (EGFR) inhibitor. EGFR is a tyrosine kinase that activates MAPK, JNK, and Akt pathways, and is an important mediator of several types of cancer.
价 格:¥电议型 号:T19814产 地:中国大陆
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T130893Teucryeminone;化合物 TeucryeminoneTeucryeminone
Teucryeminone is a useful organic compound for research related to life sciences and the catalog number is T130893.
价 格:¥电议型 号:T130893产 地:中国大陆
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T12055MK 0893;化合物 T12055MK 0893
MK 0893 is a potent, selective antagonist of glucagon receptor.
价 格:¥电议型 号:T12055产 地:中国大陆
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T10893CS-722 Free base;化合物CS-722 Free baseCS-722 Free base
CS-722 Free base is a synthetic central muscle relaxant with muscle relaxant activity and inhibitory effect on spinal reflex. CS-722 Free base may inhibit spontaneous inhibitory post-synaptic current and excitatory post-synaptic current in hippocampal culture by inhibiting sodium current and calcium current.
价 格:¥电议型 号:T10893产 地:中国大陆
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T0893Tinidazole;替硝唑CP12574;替硝唑|||CP12574
Tinidazole (CP12574)a is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole´s nitro group, in turn, is reduced via the parasite ferredoxin, thereby generating a series of free nitro radicals including nitro anions. Toxicity is achieved via depletion of sulfhydryl groups and DNA strand breaks with multiple
价 格:¥电议型 号:T0893产 地:中国大陆