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T12101MPP dihydrochloride (289726-02-9 Free base)化合物MPP dihydrochloride (289726-02-9 Free base)MPP dihydro
MPP dihydrochloride is a highly selective antagonist of estrogen receptor alpha (ERα).
价 格:¥电议型 号:T12101产 地:中国大陆
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T12095Monomethyl fumarate;富马酸单甲酯Monomethyl fumarate
Monomethyl fumarate is a potent agonist of GPR109A .
价 格:¥电议型 号:T12095产 地:中国大陆
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T12091LMM-589 TFA;化合物 T12091LMM-589 TFA
MM-589 TFA is a potent WD repeat domain 5 (WDR5)inhibitor and mixed lineage leukemia (MLL) protein-protein interaction.
价 格:¥电议型 号:T12091L产 地:中国大陆
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T1209Flunixin meglumine氟尼辛葡甲胺Banamine|||Finadyne|||Flunixin meglumin|||氟尼辛葡甲胺
Flunixin meglumine (Banamine) is an effective inhibitor of the enzyme cyclooxygenase with anti-inflammatory and antipyretic activity.
价 格:¥电议型 号:T1209产 地:中国大陆
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T12088Mofegiline hydrochloride;化合物 T12088MDL72974A;MDL72974A
Mofegiline hydrochloride is a potent and selective enzyme-activated irreversible MAO-B inhibitor.
价 格:¥电议型 号:T12088产 地:中国大陆
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T12081MMAF-OMe;化合物MMAF-OMeMonomethyl auristatin F methyl ester;Monomethyl auristatin F methyl ester
MMAF-OMe (Monomethyl auristatin F methyl ester) is an antitubulin agent which inhibits several tumor cell lines with IC50s of 0.056 nM, 0.166 nM, 0.183 nM, and 0.449 nM for MDAMB435/5T4, MDAMB361DYT2, MDAMB468, and Raji (5T4-) cell lines, respectively. MMAF-Ome is also an ADC cytotoxin.
价 格:¥电议型 号:T12081产 地:中国大陆
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T12056MK-0941 free base;MK-0941 FREE BASEMK-0941 free base
MK-0941 free base is an orally active glucokinase activator, exhibiting strong glucose-lowering activity and is a potential therapeutic agent for treatment of type 2 diabetes.
价 格:¥电议型 号:T12056产 地:中国大陆
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T12054LMK-0249 FA;MK-0249 甲酸盐MK-0249 FA(862309-06-6 Free base);MK-0249 FA(862309-06-6 Free base)
MK-0249 FA is an orally active, selective and potent histamine H3 inverse agonist for the study of attention deficit, hyperactivity disorder neurodivergent and cognitive disorders in adults.
价 格:¥电议型 号:T12054L产 地:中国大陆
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T12041MIM1;化合物MIM1Inhibitor of Mcl-1;Inhibitor of Mcl-1
MIM1 (Inhibitor of Mcl-1) is an myeloid cell factor 1 (Mcl-1) inhibitor.
价 格:¥电议型 号:T12041产 地:中国大陆
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T12037Mifamurtide米伐木肽L-MTP-PE|||MTP-PE|||CGP 19835|||米伐木肽
Mifamurtide is a drug against osteosarcoma, is an immunomodulator with antitumor effects.
价 格:¥电议型 号:T12037产 地:中国大陆
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T12032Mibefradil dihydrochloride;盐酸米贝地尔Ro 40-5967 (dihydrochloride);盐酸米贝地尔|||Ro 40-5967 (dihydrochloride)|
Mibefradil dihydrochloride (Ro 40-5967 (dihydrochloride)) is an blocker of calcium channel with moderate selectivity for T-type Ca2+ channels (T-type and L-type currents with IC50s of 2.7 μM and 18.6 μM, respectively).
价 格:¥电议型 号:T12032产 地:中国大陆
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T12026MF 5137;化合物 T12026MF 5137
MF 5137 is an effective antimicrobial agent.
价 格:¥电议型 号:T12026产 地:中国大陆
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T12025MFZ 10-7 hydrochloride;化合物 T12025MFZ 10-7 hydrochloride
MFZ 10-7 hydrochloride is a highly potent and selective negative allosteric modulator of mGluR5 NAM
价 格:¥电议型 号:T12025产 地:中国大陆
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T12024MF-094;化合物MF-094MF-094
MF-094 is a potent and selective inhibitor of USP30 with IC50 of 120 nM.
价 格:¥电议型 号:T12024产 地:中国大陆
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T12021Metofenazate;化合物 T12021Methophenazine;Methophenazine
Metofenazate is an selective inhibitor of calmodulin .
价 格:¥电议型 号:T12021产 地:中国大陆
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T11991Mefentrifluconazole氯氟醚菌唑CYPs|||aromatase|||Inhibitor
Mefentrifluconazole is a potent, selective and orally active fungal CYP51 (Kd= 0.5 nM) inhibitor, but shows less inhibitory activity on human aromatase (IC50=0.92 μM). Mefentrifluconazole is a novel azole derivative and used as an agrochemical broad-spectrum antifungal agent.
价 格:¥电议型 号:T11991产 地:中国大陆
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T11990Meclofenamic acid甲氯芬那酸甲氯芬那酸|||Meclofenamate
Meclofenamic acid (Meclofenamate) is a non-selective gap-junction blocker and a selective fat mass and obesity-associated (FTO) enzyme inhibitor. Meclofenamic acid has anti-inflammatory activities.
价 格:¥电议型 号:T11990产 地:中国大陆
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T11951Mavoglurant racemate;化合物 T11951AFQ-056 racemate;AFQ-056 racemate
Mavoglurant is a novel, non-competitive mGlu5 receptor antagonist. Mavoglurant (racemate) is the racemate of mavoglurant.
价 格:¥电议型 号:T11951产 地:中国大陆
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T11948Masupirdine free base;化合物 MasupirdineMasupirdine|||SUVN-502 free base;Masupirdine|||SUVN-502 free ba
Masupirdine free base (SUVN-502 free base) is an orally available 5-HT6 receptor antagonist that crosses the blood-brain barrier and has a Ki value of 2.04 nM for the human 5-HT6 receptor.Masupirdine free base is potent and selective with multiple targets. Masupirdine free base is highly potent, selective and inhibits multiple targets.Masupirdine free base can be used in the study of neurological disorders such as Alzheimer´s disease.
价 格:¥电议型 号:T11948产 地:中国大陆
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T11941Manitimus;玛尼莫司FK778;FK778
Manitimus (FK778) is an inhibitor of dehydroorotate dehydrogenase and an immunosuppressant with immunosuppressive and antiproliferative activity, prevents vascular remodeling after mechanical endothelial injury, and can be used to study immune dysfunction.
价 格:¥电议型 号:T11941产 地:中国大陆