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T1474Otilonium bromideOtilonium bromide,SP63,Octylonium bromide
Otilonium Bromide, an antimuscarinic, is utilized as a spasmolytic agent.
价 格：￥电议型 号：T1474产 地：美洲
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T14763BoNT-IN-1BoNT-IN-1
BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (BoNTA LC) with IC50 of 0.9 uM. IC50 value: 0.9 uM Target: BoNT in vitro: BoNT-IN-1 targets BoNT/A LC enzymatic activity. Which is highly efficient in vitro, BoNT-IN-1 has good property
价 格：￥电议型 号：T14763产 地：美洲
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T15163DPC-681DPC-681,DPH-153893,
DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).
价 格：￥电议型 号：T15163产 地：美洲
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T15263Selisistat R-enantiomerSelisistat R-enantiomer,EX-527 (R-enantiomer),
Selisistat R-enantiomer is much less active R-enantiomer of Selisistat (IC50 of > 100 μM for SIRT1).
价 格：￥电议型 号：T15263产 地：美洲
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T15560IloprostIloprost,Ciloprost,ZK 36374
Iloprost is a synthetic analogue of prostacyclin PGI2. Iloprost is a stable carbacyclin derivative of prostacyclin, was studied during electrically-induced coronary artery thrombosis in the open chest anesthetized pig. Iloprost is a stable prostacyclin an
价 格：￥电议型 号：T15560产 地：美洲
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T15592IPI-3063IPI-3063
IPI-3063 is an effective and selective inhibitor of PI3K p110δ (IC50: 2.5?±?1.2 nM).
价 格：￥电议型 号：T15592产 地：美洲
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T1563NifuroxazideNifuroxazide,Nifuroxazid,Dicoferin
Nifuroxazide is an orally available and cell-permeable nitrofuran-based antidiarrheal agent. It has the inhibitory effect against the activation of cellular STAT1/3/5 transcription.
价 格：￥电议型 号：T1563产 地：美洲
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T15632JW 642JW 642
JW 642 is an effective inhibitor of monoacylglycerol lipase (MAGL) (IC50: 7.6, 14, and 3.7 nM for inhibition of MAGL in mouse, rat, and human brain membranes, respectively).
价 格：￥电议型 号：T15632产 地：美洲
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T15633JW74JW74
JW74 antagonizes LiCl-induced activation of the canonical Wnt signaling (IC50: 420 nM).
价 格：￥电议型 号：T15633产 地：美洲
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T15635JZP-430JZP-430
JZP-430 is an effective, highly selective, irreversible inhibitor of α/β-hydrolase domain 6 (ABHD6) (IC50: 44 nM). It also shows ~230-fold selectivity over fatty acid amide hydrolase (FAAH) and lysosomal acid lipase (LAL).
价 格：￥电议型 号：T15635产 地：美洲
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T15636K-252aK-252a,SF2370,Antibiotic K 252a
K-252a is an effective inhibitor (IC50 of 3 nM) of the tyrosine-protein kinase (TRK) activity of the NGF receptor gp140trk, the product of the trk proto-oncogene. K-252a is a staurosporine analog isolated from Nocardiopsis sp. soil fungi. K-252a inhibits
价 格：￥电议型 号：T15636产 地：美洲
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T15639K-756K-756
K-756 is a direct and selective inhibitor of tankyrase (TNKS), which inhibits the ADP-ribosylation activity of TNKS1 and TNKS2 (IC50s: 31 and 36 nM, respectively).
价 格：￥电议型 号：T15639产 地：美洲
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T16070MF63MF63
MF63 is a selective mPGES-1 inhibitor (IC50: 0.9 nM and 1.3 nM for pig mPGES-1 and human mPGES-1 enzyme, respectively).
价 格：￥电议型 号：T16070产 地：美洲
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T1616Cefotiam hydrochlorideCefotiam hydrochloride,SCE-963 hydrochloride,Cefotiam dihydrochloride
Cefotiam Hydrochloride is the hydrochloride salt form of cefotiam, a third-generation, semi-synthetic, beta-lactam cephalosporin antibiotic with antibacterial activity. Cefotiam binds to penicillin-binding proteins (PBPs), transpeptidases that are respons
价 格：￥电议型 号：T1616产 地：美洲
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T16163MV1MV1
MV1 is an antagonist of IAP. When combined with HaloTag ligand, MV1 causes protein knockdown of HaloTag-fused proteins.
价 格：￥电议型 号：T16163产 地：美洲
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T1630TioproninTiopronin,Acadione,Captimer
Tiopronin, a sulfhydryl acylated derivative of glycine, leads to a reduction in urinary cystine concentration and subsequently reduces cystine stone formation.
价 格：￥电议型 号：T1630产 地：美洲
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T1631SulbactamSulbactam,CP45899,
Sulbactam is a semi-synthetic beta-lactamase inhibitor. The beta-lactam ring of sulbactam irreversibly binds to beta-lactamase at or near its active site, thereby blocking enzyme activity and preventing metabolism of other beta-lactam antibiotics by the e
价 格：￥电议型 号：T1631产 地：美洲
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T16312NH2-PEG3NH2-PEG3,PROTAC Linker 35,
NH2-PEG3 (PROTAC Linker 35) is a PROTAC linker, which belongs to a polyethylene glycol (PEG) linker. NH2-PEG3 (PROTAC Linker 35) can be used in the synthesis of the PROTAC (β-NF-JQ1)[1].
价 格：￥电议型 号：T16312产 地：美洲
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T1632AmitrazAmitraz,BTS-27419,NSC 324552
AMITRAZ is a white monoclinic crystals. Melting point 187-189°F (86-87°C). Insoluble in water. Used as an acaricide, insecticide and treatment of demodectic mange in dogs.
价 格：￥电议型 号：T1632产 地：美洲
