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T24622PF-06679142;化合物 T24622PF06679142|||PF-6679142|||PF6679142|||PF 6679142;PF06679142|||PF-6679142|||PF6
PF-06679142 is an effective AMPK activator. PF-06679142 exhibited robust activation of AMPK in rat kidneys as well as desirable oral absorption.
价 格:¥电议型 号:T24622产 地:中国大陆
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T24555NSC666715;化合物 T24555NSC 666715|||NSC-666715;NSC 666715|||NSC-666715
NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.
价 格:¥电议型 号:T24555产 地:中国大陆
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T24491MMV-667492;化合物 T24491MMV667492;MMV667492
MMV-667492 is an effective inhibitor of Ezrin.
价 格:¥电议型 号:T24491产 地:中国大陆
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T24290L 366763;化合物 T24290L366,763|||L-366,763|||L-366763|||L366763|||L 366,763;L366,763|||L-366,763|||L-36
L 366763 is an antagonist of the peptidyl fibrinogen receptor.
价 格:¥电议型 号:T24290产 地:中国大陆
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T23863CB-6673567;化合物 T23863CB 6673567;CB 6673567
CB-6673567 is a selective inhibitor of adenylyl cyclase.
价 格:¥电议型 号:T23863产 地:中国大陆
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T23667AGN-201904;化合物 AGN-201904AGN201904|||AGN 201904;AGN201904|||AGN 201904
AGN-201904 is a proton pump inhibitor, an omeprazole prodrug, which delays aging and may be used for the prevention and treatment of peptic ulcers.
价 格:¥电议型 号:T23667产 地:中国大陆
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T2332Elvitegravir;埃替格韦GS-9137|||EVG|||D06677|||JTK-303;埃替格韦|||GS-9137|||EVG|||D06677|||JTK-303
Elvitegravir (JTK-303) is a Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor. The mechanism of action of elvitegravir is as an HIV Integrase Inhibitor, and Cytochrome P450 2C9 Inducer.
价 格:¥电议型 号:T2332产 地:中国大陆
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T22667CID 5951923;化合物CID 5951923CID 5951923
CID 5951923 is an inhibitor of KLF5 transcription factor with an IC50 of 603 nM.
价 格:¥电议型 号:T22667产 地:中国大陆
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T22416RO495;化合物RO495CS-2667;CS-2667
RO495 (CS-2667), a potent inhibitor of TYK2, inhibits TYK2 with IC50 of 1.5nM as tested in cell-based pharmacological assays
价 格:¥电议型 号:T22416产 地:中国大陆
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T21667FAUC-365;化合物FAUC-365FAUC-365 Benzo[b]thiophene-2-carboxylic acid {4-[4-(2,3-dichloro-nphenyl)-piper
FAUC-365 is a D3 dopamine receptor agonist.
价 格:¥电议型 号:T21667产 地:中国大陆
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T20906MGK-264;化合物 T20906NSC 36678|||NSC 406879|||ENT 8184;NSC 36678|||NSC 406879|||ENT 8184
MGK-264, a dicarboxamide synergist, is used to enhance the effects of pesticides. when used in combination with sublethal doses of a variety of plant-derived molluscicides, it also decreases the fecundity of adult L. acuminata and reduces survival of the offspring after hatching.
价 格:¥电议型 号:T20906产 地:中国大陆
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T20667Racemic Naproxen化合物 T20667DL-Naproxen|||DL Naproxen
Racemic Naproxen is a biochemical substance.
价 格:¥电议型 号:T20667产 地:中国大陆
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T20563PD-166793;化合物PD-166793PD-166793-0000|||PD 166793|||PD166793;PD-166793-0000|||PD 166793|||PD166793
PD-166793 is an orally active, potent and selective MMP inhibitor with inhibitory effects on MMP-2, MMP-3 and MMP-13.PD-166793 ameliorates myocardial ischemia and reperfusion injury in a rat model of heart failure.PD-166793 is an orally active, potent and selective MMP inhibitor with inhibitory effects on MMP-2, MMP-3, and MMP-13.
价 格:¥电议型 号:T20563产 地:中国大陆
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T20333Diallyl phthalate;化合物 T20333NSC 7667|||NSC7667|||NSC-7667;NSC 7667|||NSC7667|||NSC-7667
Diallyl phthalate suppresses algae growth.
价 格:¥电议型 号:T20333产 地:中国大陆
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T19989Imazamethabenz;化合物 T19989Imazamethabenz-methyl|||Assert|||HSDB 6675|||Dagger;Imazamethabenz-methyl||
Imazamethabenz is a herbicide. Imazamethabenz-methyl is used on cereals and sunflowers, especially against wild oat. Activity and selectivity are due to differential de-esterification to the active parent acid in target and crop species.
价 格:¥电议型 号:T19989产 地:中国大陆
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T1984LCinaciguat hydrochloride;化合物 T1984LBAY582667|||BAY58-2667|||BAY 582667|||BAY-582667|||BAY 58-2667|||
Cinaciguat( BAY582667, BAY58-2667) is a soluble guanosine cyclase activator that can prevent cardiac dysfunction in rat models of type 1 diabetes.
价 格:¥电议型 号:T1984L产 地:中国大陆
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T1984Cinaciguat;化合物CinaciguatBAY 58-2667;BAY 58-2667
Cinaciguat (BAY 58-2667) (BAY 58-2667) is the first of a new class of soluble guanylate cyclase (sGC) activators in Clinicalal development for acute decompensated heart failure.
价 格:¥电议型 号:T1984产 地:中国大陆
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T19771SXT1596;化合物 T19771NSC-65667|||SXT-1596|||NSC 65667|||SXT 1596|||NSC65667;NSC-65667|||SXT-1596|||NSC
SXT1596 is a novel SS18-SSX/TLE1 interaction inhibitor. SXT1596 reduces cell viability and reactivates EGR1 expression in synovial sarcoma.
价 格:¥电议型 号:T19771产 地:中国大陆
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T19667R-138727;化合物 T19667Prasugrel active metabolite;Prasugrel active metabolite
R-138727 is a novel P2Y12 receptor inhibitor.
价 格:¥电议型 号:T19667产 地:中国大陆
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T18667(S,R,S)-AHPC-C5-COOH;化合物 T18667VH032-C5-COOH;VH032-C5-COOH
(S,R,S)-AHPC-C5-COOH (VH032-C5-COOH) is a synthesized conjugate designed for E3 ligase ligand-linker applications, combining the VH032 VHL-based ligand with a linker for PROTAC development. VH-032 acts as a selective and potent VHL/HIF-1α interaction inhibitor, with a dissociation constant (Kd) of 185 nM, offering potential in anemia and ischemic diseases research[1].
价 格:¥电议型 号:T18667产 地:中国大陆