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T6043PF-3845PF3845；PF 3845
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
价 格：￥电议型 号：T6043产 地：中国大陆
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T4436RO1138452CAY10441
RO1138452 is a selective and orally bioavailable antagonist of prostacyclin receptor (pKi: 8.3). It antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner.
价 格：￥电议型 号：T4436产 地：中国大陆
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T3845(+)-GallocatechinGallocatechol；D-Gallocatechin；没食子儿茶素没食子酸酯
Gallocatechin possesses free radical scavenging ability. Gallocatechin has moderate affinity to the human cannabinoid receptor.
价 格：￥电议型 号：T3845产 地：中国大陆
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T6043PF-3845PF-3845,PF3845,PF 3845
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
价 格：￥电议型 号：T6043产 地：美洲
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T838458-(4-azidophenacylthio) NAD+ sodium；化合物 8-(4-azidophenacylthio) NAD+ sodiumClick Tag? 8-(4-azidophen
8-(4-Azidophenacylthio) NAD+ is a clickable variant of the essential signaling molecule and enzyme cofactor, NAD+.
价 格：￥电议型 号：T83845产 地：中国大陆
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T73845Piperaquine tetraphosphate；化合物 Piperaquine tetraphosphatePiperaquine tetraphosphate
Piperaquine tetraphosphate, a potent antimalarial agent, demonstrates inhibitory effects against both chloroquine-sensitive and chloroquine-resistant malaria isolates. When combined with dihydroartemisinin, it holds potential for researching chloroquine-resistant malaria [1] [2].
价 格：￥电议型 号：T73845产 地：中国大陆
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T63845ATX inhibitor 14；化合物 ATX inhibitor 14ATX inhibitor 14
ATX inhibitor 14, an indole-based carbamate derivative, is a potent inhibitor (IC50: 0.41 nM) of self-adhesive proteins (ATX) and has shown potential for research in fibrosis-related diseases.
价 格：￥电议型 号：T63845产 地：中国大陆
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T6043PF-3845；化合物PF-3845PF-3845
PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.
价 格：￥电议型 号：T6043产 地：中国大陆
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T5346S63845；化合物S63845S63845
S63845 is a selective MCL-1 inhibitor(Kd: 0.19 nM)
价 格：￥电议型 号：T5346产 地：中国大陆
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T4436RO1138452；化合物RO1138452CAY10441；CAY10441
RO1138452 (CAY10441) is a selective and orally bioavailable antagonist of prostacyclin receptor (pKi: 8.3). It antagonizes the carbaprostacyclin-induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-dependent manner. Likewise, it inhibits the binding of tritiated iloprost to rodent neuroblastoma cells with a Ki of about 1.5 nM. At levels between 2-20 mg/kg in rats, CAY10441 shows significant analgesic activity in standard antinociceptive assays [
价 格：￥电议型 号：T4436产 地：中国大陆
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T38459Chromium(III) acetate醋酸铬Chromium triacetate|||Chromic acetate|||Chromium acetate
Chromium(III) acetate （Chromium acetate） is a small molecule ionic crosslinker that is used as a feedstock for the synthesis of other compounds.
价 格：￥电议型 号：T38459产 地：中国大陆
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T38458Faropenem；FaropenemFaropenem
Faropenem, a highly efficacious and orally bioavailable beta-lactam antibiotic, exhibits an extensive range of in vitro antimicrobial activity against diverse gram-positive and -negative aerobes and anaerobes. Notably, Faropenem possesses inherent resistance to hydrolysis by virtually all beta-lactamases, including extended-spectrum beta-lactamases and AmpC beta-lactamases. Moreover, Faropenem has been developed as an oral prodrug, namely faropenem medoxomil, for the investigation of respiratory
价 格：￥电议型 号：T38458产 地：中国大陆
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T38457Lenalidomide-4-OH；Lenalidomide-4-OHLenalidomide-4-OH
Lenalidomide-4-OH is a cereblon (CRBN) ligand derived from Lenalidomide, utilized in the recruitment of the CRBN protein. It can be conjugated to the protein ligand via a linker, facilitating the formation of PROTAC.
价 格：￥电议型 号：T38457产 地：中国大陆
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T38456Tribenuron；TribenuronTribenuron
Tribenuron, a slow acting sulfonylurea herbicide, controls broadleaf weed.
价 格：￥电议型 号：T38456产 地：中国大陆
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T38455m-PEG20-alcohol；m-PEG20-alcoholm-PEG20-alcohol；m-PEG20-alcohol
m-PEG20-alcohol is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T38455产 地：中国大陆
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T38454N6-Methyl-dA phosphoramidite；N6-Methyl-dA phosphoramiditeN6-Methyl-dA phosphoramidite；N6-Methyl-dA p
N6-Methyl-dA phosphoramidite can be used in the synthesis of oligodeoxyribonucleotides.
价 格：￥电议型 号：T38454产 地：中国大陆
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T38453Bromo-PEG7-azide；Bromo-PEG7-azideBromo-PEG7-azide；Bromo-PEG7-azide
Bromo-PEG7-azide is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T38453产 地：中国大陆
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T38452L-threo Lysosphingomyelin (d18:1)；L-threo Lysosphingomyelin (d18:1)L-threo-Sphingosylphosphorylcholi
L-threo Lysosphingomyelin (d18:1) (L-threo-Sphingosylphosphorylcholine) is a naturally occurring bioactive sphingolipid. It acts as a potent agonist for S1P receptors, with EC50 values of 19.3, 131.8, and 313.3 nM for hS1P1, hS1P3, and hS1P2, respectively.
价 格：￥电议型 号：T38452产 地：中国大陆
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T38451Clodinafop-propargyl；Clodinafop-propargylClodinafop-propargyl
Clodinafop-propargyl, a prominent member of aryloxyphenoxy-propionate herbicides, is employed for postemergence management of annual grasses in cereals, such as Avena, Lolium, Setaria, Phalaris, and Alopecurus spp.
价 格：￥电议型 号：T38451产 地：中国大陆
