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T20056Oxolamine；化合物 T20056BRN 0527181|||Bredon|||AF-438|||Ossolamina|||AF 438；BRN 0527181|||Bredon|||AF-43
Oxolamine is an agent of a cough suppressant.
价 格：￥电议型 号：T20056产 地：中国大陆
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T19271DAOS化合物DAOSSodium 3-((3,5-dimethoxyphenyl)(ethyl)amino)-2-hydroxypropane-1-sulfonate
DAOS (Sodium 3-((3,5-dimethoxyphenyl)(ethyl)amino)-2-hydroxypropane-1-sulfonate),Trinder´s reagent, is a new type of highly water-soluble aniline derivative. It is widely used in diagnostic tests and biochemical tests.
价 格：￥电议型 号：T19271产 地：中国大陆
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T18271Mal-PEG12-alcohol；化合物 T18271Mal-PEG12-alcohol
Mal-PEG12-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：T18271产 地：中国大陆
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T17271YKL-05-099；化合物YKL-05-099YKL-05-099
YKL-05-099 is an inhibitor of the salt-inducible kinase(SIK1 and SIK3 ; IC50s: 10 and 30 nM, respectively). It has a slightly less potent SIK2-inhibitory (IC50:40 nM).
价 格：￥电议型 号：T17271产 地：中国大陆
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T17269Y-27152；化合物 T17269Y-27152
Y-27152 is a prodrug of the KATP (Kir6) channel opener Y-26763 and is a long-acting K+ channel opener.
价 格：￥电议型 号：T17269产 地：中国大陆
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T17243VU0463271；化合物VU0463271N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetami
VU0463271 (N-Cyclopropyl-N-(4-methyl-2-thiazolyl)-2-[(6-phenyl-3-pyridazinyl)thio]acetamide) is a potent and selective antagonist of the neuronal-specific potassium-chloride cotransporter 2 (KCC2), with an IC50 of 61 nM and >100-fold selectivity versus the closely related Na-K-2Cl cotransporter 1 (NKCC1) and no activity in a larger panel of GPCRs, ion channels, and transporters.
价 格：￥电议型 号：T17243产 地：中国大陆
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T16271Napropamide敌草胺敌草胺|||Napropamid
Napropamide is a selective systemic amide herbicide. Napropamide is used to control a number of annual grasses and broad-leaved weeds.
价 格：￥电议型 号：T16271产 地：中国大陆
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T15271Denifanstat；化合物FASN-IN-2FASN-IN-2|||TVB2640|||TVB-2640；FASN-IN-2|||TVB2640|||TVB-2640
Denifanstat (FASN-IN-2) is a Fatty Acid Synthase (FASN) inhibitor(IC50 of 0.052 μM and an EC50 of 0.072 μM),with potential antineoplastic activity.
价 格：￥电议型 号：T15271产 地：中国大陆
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T14504BAY 38-7271；化合物 T14504BAY 38-7271
BAY 38-7271 has strong neuroprotective properties.[1] BAY 38-7271 is selective and highly potent and cannabinoid CB1/CB2 receptor agonist. With Kis of 1.85 nM and 5.96 nM for recombinant human CB1 receptor and CB2 receptor, respectively.
价 格：￥电议型 号：T14504产 地：中国大陆
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T14487AZM475271；化合物 T14487M475271；M475271
AZM475271 is a potent and selective inhibitor of Src kinase(IC50 : 5 nM)
价 格：￥电议型 号：T14487产 地：中国大陆
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T14271Aminooxy-PEG4-alcohol；化合物Aminooxy-PEG4-alcoholAminooxy-PEG4-alcohol
Aminooxy-PEG4-alcohol is both a non-cleavable 4-unit PEG ADC linker and a PEG-based PROTAC linker.
价 格：￥电议型 号：T14271产 地：中国大陆
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T14075A-802715；化合物A-802715A-802715
A-802715 is a novel methylxanthine derivative that decreases the endogenous formation and blood levels of pro-inflammatory substances and increases the formation and blood levels of anti-inflammatory substances such as interleukin 10 receptor and tumor necrosis factor receptor.
价 格：￥电议型 号：T14075产 地：中国大陆
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T13409LZK824859 hydrochloride (2271122-53-1 free base)；化合物 T13409LZK824859 hydrochloride；ZK824859 hydrochlo
ZK824859 hydrochloride is an oral available and selective inhibitor of urokinase plasminogen activator (uPA)(IC50s of 79 nM, 1580 nM and 1330 nM for human uPA, tPA, and plasmin, respectively).
价 格：￥电议型 号：T13409L产 地：中国大陆
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T13271USP7-IN-6；化合物 T13271USP7-IN-6
USP7-IN-6 is a potent inhibitor of ubiquitin-specific protease 7 (USP7, IC50: 6.8 nM).
价 格：￥电议型 号：T13271产 地：中国大陆
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T131271Compound N039-0029；化合物 N039-0029Compound N039-0029
Compound N039-0029 is a useful organic compound for research related to life sciences and the catalog number is T131271.
价 格：￥电议型 号：T131271产 地：中国大陆
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T12783RWJ 50271；化合物RWJ 50271RWJ 50271
RWJ 50271 is a selective lymphocyte function-associated antigen-1/intercellular adhesion molecule-1(LFA-1/ICAM-1) interaction inhibitor( IC50 of 5.0 μM in HL60 cells).
价 格：￥电议型 号：T12783产 地：中国大陆
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T12719RG7834；化合物RG7834RO 7020322；RO 7020322
RG7834 (RO 7020322) is a highly selective and orally bioavailable inhibitor of HBV(HBsAg and HBeAg and HBV DNA with IC50s of 2.8, 2.6, and 3.2 nM, respectively, in dHepaRG Cells).
价 格：￥电议型 号：T12719产 地：中国大陆
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T12718LRG7800化合物RG7800RO6885247
RG7800 (RO6885247) has the potential for spinal muscular atrophy treatment. RG7800 is an SMN2 splicing modifier.
价 格：￥电议型 号：T12718L产 地：中国大陆
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T12718RG7800 hydrochloride (1449598-06-4 free base)；化合物 T12718RO6885247 hydrochloride|||RG7800 hydrochlori
RG7800 hydrochloride is an orally active modulator of SMN2 splicing.
价 格：￥电议型 号：T12718产 地：中国大陆
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T12717Basimglurant；化合物BasimglurantCTEP Derivative|||RG7090；CTEP Derivative|||RG7090
Basimglurant (CTEP Derivative) is a potent, selective and orally available modulator of mGlu5 negative allosteric(Kd of 1.1 nM).
价 格：￥电议型 号：T12717产 地：中国大陆
