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T8822JNJ-5207852 dihydrochlorideInhibitor,toxicity,JNJ5207852,inhibit,low,JNJ 5207852,sleep,REM,JNJ-52078
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
价 格:¥电议型 号:T8822产 地:中国大陆
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T16889SJ572403
SJ572403 is an inhibitor of disordered protein p27 with Kd of 2.2 mM for specific regions within the D2 subdomain of p27-KID. SJ572403 can be used in studies about diseases with intrinsically disordered proteins.
价 格:¥电议型 号:T16889产 地:中国大陆
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T37806JNJ-55308942JNJ 55308942,JNJ55308942
JNJ-55308942 is a selective and brain-penetrant antagonist of P2X7 functional with IC50s of 10 and 15 nM and Kis of 7.1 and 2.9 nM for hP2X7 and rP2X7, respectively.
价 格:¥电议型 号:T37806产 地:中国大陆
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T8374LJ570inhibit,Peroxisome proliferator-activated receptors,LJ-570,LJ 570,LJ570,Inhibitor,PPAR
LJ570 is the first PPARα/γ dual agonist (PPARα,PPARγ with EC50s of 1.05 and 0.12 μM, respectively[)
价 格:¥电议型 号:T8374产 地:中国大陆
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T6933PeficitinibJAK,Janus kinase,lymphocytes,JNJ 54781532,Peficitinib,JNJ54781532,Inhibitor,rheumatoid ar
Peficitinib (ASP015K, JNJ-54781532) is an orally bioavailable JAK inhibitor. Phase 3.
价 格:¥电议型 号:T6933产 地:中国大陆
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T7413JNJ-5207852sleep,low,JNJ5207852,Histamine Receptor,JNJ-5207852,JNJ 5207852,Inhibitor,REM,toxicity,in
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
价 格:¥电议型 号:T7413产 地:中国大陆
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T8374LJ570;化合物LJ570LJ570
LJ570 is the first PPARα/γ dual agonist (PPARα,PPARγ with EC50s of 1.05 and 0.12 μM, respectively[)
价 格:¥电议型 号:T8374产 地:中国大陆
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T82020J5 peptide;化合物 J5 peptideMyelin basic protein (85-99) antagonist;Myelin basic protein (85-99) antago
J5 peptide, an MBP inhibitor, competitively inhibits the binding of MBP 85-99 to HLA-DR2, and mitigates PLP 139-151/MBP 85-99-induced experimental autoimmune encephalomyelitis (EAE) in mice. It is utilized in research pertaining to inflammatory and immune diseases [1].
价 格:¥电议型 号:T82020产 地:中国大陆
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T71864SJ572710;化合物 SJ572710SJ572710
SJ572710 is an inhibitor of the disordered protein, p27(Kip1).
价 格:¥电议型 号:T71864产 地:中国大陆
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T604225-C-heptyl-DNJ;化合物 5-C-heptyl-DNJ5-C-heptyl-DNJ
5-heptyl-DNJ is an effective GAA agonist with a Ki of 0.0047 μM. 5-C-heptyl-DNJ increases GAA activities through chaperrone effects [1].
价 格:¥电议型 号:T60422产 地:中国大陆
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T31585D-Tocotrienol;化合物 T31585D Tocotrienol|||DTocotrienol|||Tocotrienol, D-|||J509.403H;D Tocotrienol|||D
Tocotrienols are certain members of the vitamin E family.
价 格:¥电议型 号:T31585产 地:中国大陆
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T30524BMS-442606;化合物 T30524UNII-97L718J5KP|||97L718J5KP|||ZINC22060380;UNII-97L718J5KP|||97L718J5KP|||ZINC
BMS-442606 is a 5-HT1A part agonist.
价 格:¥电议型 号:T30524产 地:中国大陆
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T27687JNJ525;化合物 T27687JNJ 525|||JNJ-525;JNJ 525|||JNJ-525
JNJ525 is an inhibitor of TNFα. JNJ525 inhibits protein function via an aggregation-based mechanism. JNJ525 prevents the formation of TNFα complexes with TNFR1 and TNFR2, the apparent IC50 values for the inhibition of complex formation are 1.2 ± 0.2 μM and 1.1 ± 0.1 μM respectively in the TR-FRET assay.
价 格:¥电议型 号:T27687产 地:中国大陆
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T27250Elarofiban;艾罗非班RWJ-53308|||RWJ 53308|||RWJ53308;RWJ-53308|||RWJ 53308|||RWJ53308
Elarofiban(RWJ-53308) is a novel and orally active GPIIb/IIIa antagonist.
价 格:¥电议型 号:T27250产 地:中国大陆
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T25559JNJ-56022486;化合物 T25559JNJ56022486;JNJ56022486
JNJ-56022486 is a selective TARP γ?8 AMPA receptor modulator.
价 格:¥电议型 号:T25559产 地:中国大陆
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T22821GSK J5;化合物GSK J5GSK-J5|||GSKJ5;GSK-J5|||GSKJ5
GSK J5 is an inhibitor of schistosomes and helminths and is often used as a trematode insecticide.GSK J5 promotes schistosome mortality in a dose- and time-dependent manner.GSK J5 increases the mortality rate of schistosomes and decreases the viability of adult worms.GSK J5 is an inhibitor of schistosomes and helminths and is often used as a trematode insecticide.
价 格:¥电议型 号:T22821产 地:中国大陆
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T22820GSK J5 HCl (1394854-51-3 free base);化合物 T22820GSK J5 HCl;GSK J5 HCl
GSK J5 HCl is the hydrochloride form of GSK J5. GSK J5 is an inactive isomer of GSK J4 and a cell-permeable ester derivative of inactive control GSK J2.
价 格:¥电议型 号:T22820产 地:中国大陆
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T16889SJ572403;化合物SJ572403SJ403;SJ403
SJ572403 is an inhibitor of disordered protein p27 with Kd of 2.2 mM for specific regions within the D2 subdomain of p27-KID. SJ572403 can be used in studies about diseases with intrinsically disordered proteins.
价 格:¥电议型 号:T16889产 地:中国大陆
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T15630Tilmacoxib;替马考昔RWJ57504|||JTP19605|||JTE522;RWJ57504|||JTP19605|||替马考昔|||JTE522
Tilmacoxib is a highly selective, time-dependent, and irreversible inhibitor of human COX-2 ( IC50: 85 nM in an enzyme assay).
价 格:¥电议型 号:T15630产 地:中国大陆