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T64643Rh2(S-TCPTAD)4；化合物 Rh2(S-TCPTAD)4Rh2(S-TCPTAD)4
Rh2(S-TCPTAD)4 is a useful organic compound for research related to life sciences and the catalog number is T64643.
价 格：￥电议型 号：T64643产 地：中国大陆
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T64139TCMDC-135051 TFA；化合物 TCMDC-135051 TFATCMDC-135051 TFA
TCMDC-135051 TFA is a potent, highly selective, low off-target toxicity protein kinase PfCLK3 inhibitor that exhibits antiparasitic effects with an EC50 value of 320 nM. TCMDC-135051 TFA blocks the trophozoite to lytic transition, disrupts transcription and inhibits transmission to mosquito vectors.
价 格：￥电议型 号：T64139产 地：中国大陆
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T63488TCMDC-135051 hydrochloride；化合物 TCMDC-135051 hydrochlorideTCMDC-135051 hydrochloride
TCMDC-135051 hydrochloride is a potent, highly selective, low off-target toxicity inhibitor of the protein kinase PfCLK3. TCMDC-135051 hydrochloride blocks the trophozoite to lysosome transition, disrupts transcription and inhibits transmission to mosquito vectors, exhibiting an antiparasitic effect with an EC50 value of 320 nM.
价 格：￥电议型 号：T63488产 地：中国大陆
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T63056Dovramilast；化合物 DovramilastCC-11050；CC-11050
Dovramilast (CC-11050) is an orally active phosphodiesterase 4 (PDE4) inhibitor that reduces the production of pro-inflammatory mediators and cytokines.Dovramilast is used in the study of Mycobacterium tuberculosis infections and lupus erythematosus.
价 格：￥电议型 号：T63056产 地：中国大陆
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T62588TCMDC-136230；化合物 TCMDC-136230TCMDC-136230
TCMDC-136230 is a novel inhibitor of Plasmodium calcium kinetics with minimal inhibition of haemoglobin crystallisation.
价 格：￥电议型 号：T62588产 地：中国大陆
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T62440TCMDC-125431；化合物 TCMDC-125431TCMDC-125431
TCMDC-125431 is a novel inhibitor of Plasmodium calcium kinetics with minimal inhibition of haemoglobin crystals.
价 格：￥电议型 号：T62440产 地：中国大陆
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T6214Emtricitabine恩曲他滨恩曲他滨|||FTC|||Emtriva|||BW1592
Emtricitabine (FTC) (FTC), a nucleoside reverse transcriptase inhibitor, exhibits inhibition activity against human immunodeficiency virus (HIV) and hepatitis B virus.
价 格：￥电议型 号：T6214产 地：中国大陆
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T61917TCMDC-125457；化合物 TCMDC-125457TCMDC-125457
TCMDC-125457 can effectively induce calcium redistribution, but has little effect on inhibiting heme crystallization. When TCMDC-125457 is combined with artesunate, it can effectively treat tightly synchronized artemisinin-resistant ring-stage parasites.
价 格：￥电议型 号：T61917产 地：中国大陆
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T6178PTC-209 hydrobromide；化合物PTC-209 HBrPTC-209 HBr；PTC-209 HBr
PTC-209 hydrobromide (PTC-209 HBr) is the hydrobromide salt of PTC-209, which is a potent and selective BMI-1 inhibitor with IC50 of 0.5 μM, and results in irreversible reduction of cancer-initiating cells (CICs).
价 格：￥电议型 号：T6178产 地：中国大陆
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T61531NFATc1-IN-1；化合物NFATc1-IN-1NFATc1-IN-1
NFATc1-IN-1 (also known as compound A04) is a highly effective inhibitor of osteoclast formation induced by RANKL, with an IC50 of 1.57 μM. It exerts its anti-osteoclastogenic effects by attenuating the RANKL-induced nuclear translocation of NFATc1. Due to its remarkable properties, NFATc1-IN-1 holds significant potential for advancing research related to osteoclastic diseases [1].
价 格：￥电议型 号：T61531产 地：中国大陆
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T61526Cicaprost；化合物 CicaprostCicaprost
Cicaprost (ZK 96480) is a prostacyclin receptor (IP) agonist, which induces relaxation of the artery via concentration-dependent mechanisms. Its EC50 value, determined to be 5.8 nM [1], further highlights its potency.
价 格：￥电议型 号：T61526产 地：中国大陆
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T6138TCS 359化合物TCS 359FLT3 Inhibitor
TCS 359 (FLT3 Inhibitor) is a potent FLT3 inhibitor with IC50 of 42 nM.
价 格：￥电议型 号：T6138产 地：中国大陆
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T6065Triciribine；曲西立滨VD-0002|||Tricyclic nucleoside|||NSC 154020|||API-2|||TCN；VD-0002|||Tricyclic nucleo
Triciribine (NSC-154020) is a DNA synthesis inhibitor, and it also inhibits Akt and HIV-1/2.
价 格：￥电议型 号：T6065产 地：中国大陆
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T60507Utreloxastat；化合物 UtreloxastatEPI 857|||PTC857；EPI 857|||PTC857
Utreloxastat (PTC857) is a novel 15-lipoxygenase inhibitor that can be used to study amyotrophic lateral sclerosis.
价 格：￥电议型 号：T60507产 地：中国大陆
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T60102LDimethylaminomicheliolide HCl；化合物ATC001Dimethylaminomicheliolide HCl
Dimethylaminomicheliolide HCl has potential anti-inflammatory and anti-tumor activity and inhibits the proliferation of glioblastoma cells by targeting pyruvate kinase 2 (PKM2) and reconnecting aerobic cell populations.
价 格：￥电议型 号：T60102L产 地：中国大陆
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T5815MJN110；化合物Cravatt ReagentCravatt Reagent；Cravatt Reagent
MJN110 (Cravatt Reagent) is a potent and selective MAGL inhibitor. Cravatt Reagent inhibits MAGL (IC50 = 9.1 nM). MJN110(Cravatt Reagent) Produces Opioid-Sparing Effects in a Mouse Neuropathic Pain Model.
价 格：￥电议型 号：T5815产 地：中国大陆
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T5315TCA1；化合物TCA-1TCA-1|||TCA 1；TCA-1|||TCA 1
TCA1 (TCA 1) is a small molecule with activity against drug-resistant and persistent tuberculosis.
价 格：￥电议型 号：T5315产 地：中国大陆
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T4965LTCS-OX2-29 HCl；化合物 T4965LTCSOX 229|||TCS-OX229|||TCS OX229|||TCS OX2 29|||TCSOX-229|||TCSOX229；TCSOX
TCS-OX2-29 is a selective orexin-2 receptor antagonist (IC50 = 40 nM), which plays an important role in pain modulation.
价 格：￥电议型 号：T4965L产 地：中国大陆
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T4965TCS-OX2-29；化合物TCS-OX2-29TCS-OX2-29
TCS-OX2-29 is a potent and selective OX2 receptor antagonist (IC50: 40 nM). It displays >250-fold selectivity for OX2 over OX1.
价 格：￥电议型 号：T4965产 地：中国大陆
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T4666TCJL37；化合物 T4666TCJL37
TCJL37, a potent, selective, and orally bioavailable inhibitor of TYK2, exhibits a K i value of 1.6 nM. It is useful for researching inflammatory bowel diseases (IBD) [1].
价 格：￥电议型 号：T4666产 地：中国大陆
