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产品数：86101
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TN2345Loureirin DLoureirin D
Loureirin D is a chalcone from the herbs of Dracaena cochinchinensis.
价 格：￥电议型 号：TN2345产 地：中国大陆
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T23074NNC 63-0532
NNC 63-0532 is a potentnociceptin receptor agonist, Ki=7.3 nM, EC50=305 nM.
价 格：￥电议型 号：T23074产 地：中国大陆
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T72345-Amino-2-chloropyridine5 Amino 2 chloropyridine,5Amino2chloropyridine
5-Amino-2-chloropyridine is Pyridine intermediates
价 格：￥电议型 号：T7234产 地：中国大陆
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T60123Chimmitecan
Chimmitecan is a potent inhibitor of topoisomerase I and displays outstanding activity in vitro and in vivo.
价 格：￥电议型 号：T60123产 地：中国大陆
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T7295MiridesapGSK 2315698,GSK-2315698,Miridesap,Inhibitor,inhibit
Miridesap is a divalent crosslinker of SAP that causes rapid depletion of circulating SAP via hepatic clearance. It also produces significant reduction of SAP from cerebrospinal fluid and visceral amyloid deposits
价 格：￥电议型 号：T7295产 地：中国大陆
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T8234ML401ML401,Inhibitor,ML 401,EBI2/GPR183,inhibit,ML-401
ML401 is a selectively EBI2(GPR183) receptor antagonist(IC50 of 1.03 nM) .
价 格：￥电议型 号：T8234产 地：中国大陆
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T23003ML337
ML337 is a negative allosteric modulator of mGlu3 with an IC50 of 593 nM.
价 格：￥电议型 号：T23003产 地：中国大陆
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T40023Pomalidomide-PEG3-CO2H
Thalidomide-NH-PEG3-propionic acid is a synthesized E3 ligase ligand-linker conjugate. Thalidomide-NH-PEG3-propionic acid incorporates the Thalidomide based cereblon ligand and 3-unit PEG linker used in PROTAC technology.
价 格：￥电议型 号：T40023产 地：中国大陆
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T8323LolCDE-IN-1antibacterial,inhibit,Bacterial,LolCDEIN1,Inhibitor,LolCDE IN 1,LolCDE
LolCDE-IN-1 is an inhibitor of the Lol proteins (LolCDE) complex. LolCDE-IN-1 shows antibacterial activity.
价 格：￥电议型 号：T8323产 地：中国大陆
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T10623BSH-IN-1BSH IN 1,BSHIN1
BSH-IN-1 is a potent and covalent inhibitor of gut bacterial recombinant bile salt hydrolases (BSHs; IC50s: 108 nM and 427 nM for B. longum BSH and B. theta BSH).
价 格：￥电议型 号：T10623产 地：中国大陆
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T23889CID-663143CID 663143
CID-663143 inhibits cancer cell growth and shows microtubule-binding activity.
价 格：￥电议型 号：T23889产 地：中国大陆
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T11123DuP 105DuP 105
DuP 105 is an orally active oxazolidinone, a new class of synthetic antimicrobial agent with activity against gram-positive bacteria.
价 格：￥电议型 号：T11123产 地：中国大陆
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T7549Talnetantschizophrenia,SB223412,NK receptor,Inhibitor,hNK-2,Talnetant,Neurokinin Receptor,Tachykinin
Talnetant is a selective, competitive, brain-penetrant NK3 receptor antagonist with the ability to modulate mesolimbic and mesocortical dopaminergic neurotransmission
价 格：￥电议型 号：T7549产 地：中国大陆
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T6883SamotolisibInhibitor,mTOR,LY-3023414,Phosphoinositide 3-kinase,DNA-dependent protein kinase,inhibit,
LY3023414 is an oral ATP competitive inhibitor of the class I PI3K isoforms, DNA-PK, and mTOR. LY3023414 has been used in trials studying the treatment of Neoplasm, Solid Tumor, COLON CANCER, BREAST CANCER, and Advanced Cancer, among others.
价 格：￥电议型 号：T6883产 地：中国大陆
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T2310LCHIR-99021 HCl
Laduviglusib (CHIR-99021) monohydrochloride is a potent and selective GSK-3α/β inhibitor with IC 50 s of 10 nM and 6.7 nM. Laduviglusib monohydrochloride shows over 500-fold selectivity for GSK-3 over CDC2, ERK2 and other protein kinases. Laduviglusib monohydrochloride is also a potent Wnt/β-catenin signaling pathway activator. Laduviglusib monohydrochloride enhances mouse and human embryonic stem cells self-renewal. Laduviglusib monohydrochloride induces autophagy [1] [2] [3].
价 格：￥电议型 号：T2310L产 地：中国大陆
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T22303Dasatinib hydrochloride
Dasatinib hydrochloride (BMS-354825) hydrochloride is a highly potent, ATP competitive, orally active dual Src/Bcr-Abl inhibitor with potent antitumor activity. The Kis are 16 pM and 30 pM for Src and Bcr-Abl, respectively. Dasatinib hydrochloride hydrochloride inhibits Bcr-Abl and Src with IC50s of <1.0 nM and 0.5 nM, respectively. Dasatinib hydrochloride hydrochloride also induces Apoptosis and Autophagy.
价 格：￥电议型 号：T22303产 地：中国大陆
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T8219VU0238441mAChR,Inhibitor,VU-0238441,VU0238441,Muscarinic acetylcholine receptor,VU 0238441,inhibit
VU0238441 is agonist of Muscarinic acetylcholine receptor M5 (human) with EC50 of 2.1μM.
价 格：￥电议型 号：T8219产 地：中国大陆
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T8505SC-236SC-236,gastric,PPAR,cancer,ischemia,Liver,inhibit,allodynia,Inhibitor,fibrogenesis,neuroprotec
Sc 236 is an orally active and selective inhibitor of COX-2 (IC50 of 0.005 μM and 17.8 μM for COX-2 and COX-1, respectively).
价 格：￥电议型 号：T8505产 地：中国大陆
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TN3231PratolPratol
Pratol significantly increased melanin content and tyrosinase activity in the cells without being cytotoxic.
价 格：￥电议型 号：TN3231产 地：中国大陆
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T8329AR 231453inhibit,GPR119,AR-231453,G Protein-Coupled Receptor 119,diabetes,AR231453,AR 231453,insulin
AR 231453 is a selective and orally available GPR119 agonist,can stimulate β-cell replication and improve islet graft function.
价 格：￥电议型 号：T8329产 地：中国大陆
