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TQ0155Miglustat hydrochlorideN-Butyldeoxynojirimycin,OGT-918,type I gaucher disease,Miglustat,Miglustat hy
Miglustat hydrochloride is an inhibitor of glucosylceramide synthase and can be used for studies about Type I Gaucher disease.
价 格：￥电议型 号：TQ0155产 地：中国大陆
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T8890653-47 hydrochlorideInhibitor,transcription,65347 hydrochloride,Epigenetic Reader Domain,inhibit,CRE
653-47 hydrochloride is a potentiator, significantly potentiates the cAMP-response element binding protein (CREB) inhibitory activity of 666-15. It is also a very weak CREB inhibitor with IC50 of 26.3 μM.
价 格：￥电议型 号：T8890产 地：中国大陆
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T6390Anagrelide hydrochloridePhosphodiesterase (PDE),Anagrelide,inhibit,Inhibitor,Anagrelide hydrochlorid
Anagrelide Hydrochloride(BL4162A) is a drug used for the treatment of essential thrombocytosis.
价 格：￥电议型 号：T6390产 地：中国大陆
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TN71541H-Indole-3-ethanamine, 5-bromo-N,N-dimethyl-, hydrochloride
1H-Indole-3-ethanamine, 5-bromo-N,N-dimethyl-, hydrochloride is a marine derived natural products found in Smenospongia echina.
价 格：￥电议型 号：TN7154产 地：中国大陆
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T25282CYM 50358 hydrochloride (1314212-39-9 free base)CYM 50358 hydrochloride (1314212 39 9 free base),CYM
CYM50358 HCl is an S1P4 antagonist.
价 格：￥电议型 号：T25282产 地：中国大陆
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T23470Tracazolate hydrochloride
Tracazolate hydrochloride is a modulator of the GABAA receptor with anxiolytic and anticonvulsant activity. Tracazolate hydrochloride potentiates α1β1γ2s and α1β3γ2 with EC50s of 13.2 μM and 1.5 μM.
价 格：￥电议型 号：T23470产 地：中国大陆
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T99683-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride3Piperidinyl(1pyrrolidinyl)methanone hydrochlori
3-Piperidinyl(1-pyrrolidinyl)methanone hydrochloride can be used in the synthesis of piperidin-4-yl-urea derivatives which are MCH-R1 antagonists.
价 格：￥电议型 号：T9968产 地：中国大陆
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T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格：￥电议型 号：T6951产 地：中国大陆
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T35341NVP-BSK805 dihydrochloride
NVP-BSK805 dihydrochloride is an effective and selective inhibitor of JAK2 with IC50s of 0.5 nM, 10.76 nM, 18.68 nM, and 31.63 nM for JAK2, TYK2, JAK3, and JAK1.
价 格：￥电议型 号：T35341产 地：中国大陆
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T6940PHA-767491 hydrochloridePHA767491,PHA 767491,inhibit,CAY-10572,Cyclin dependent kinase,CDK,CAY 10572
PHA-767491 is an effective ATP-competitive dual Cdc7/CDK9 inhibitor (IC50: 10/34 nM). It has ~20-fold selectivity against GSK3-β and CDK1/2, 50-fold selectivity against CDK5 and MK2, 100-fold selectivity against CHK2 and PLK1.
价 格：￥电议型 号：T6940产 地：中国大陆
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T7117Sapropterin dihydrochloride(6R)-BH4,Sapropterin,Inhibitor,inhibit,Sapropterin dihydrochloride
Sapropterin dihydrochloride is phenylalanine hydroxylase agonist that is approved for the treatment of BH4 responsive PKU.
价 格：￥电议型 号：T7117产 地：中国大陆
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T6566Levobupivacaine hydrochlorideCNS toxicity,gastric cancer,Na channels,Erastin,Inhibitor,analgesic,ana
Levobupivacaine HCl is a reversible neuronal sodium channel inhibitor, which is the pure S(-)-enantiomer of bupivacaine. It was utilized as a long-acting local anesthetic.
价 格：￥电议型 号：T6566产 地：中国大陆
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T13890SMARCA-BD ligand 1 for Protac dihydrochlorideSMARCABD ligand 1 for Protac dihydrochloride,SMARCA BD
SMARCA-BD ligand 1 for Protac dihydrochloride binds to the BAF ATPase subunits SMARCA2, and used for degrading SMARCA2, based on PROTAC.
价 格：￥电议型 号：T13890产 地：中国大陆
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T10837Clocapramine dihydrochloride hydrateClocapramine dihydrochloride hydrate
Clocapramine dihydrochloride hydrate is an antagonist of the 5-HT2A and D2 receptors.
价 格：￥电议型 号：T10837产 地：中国大陆
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T8617GMQ hydrochlorideGMQ hydrochloride
GMQ hydrochloride is a potent and selective acid-sensing ion channel (ASIC) modulator. It activates ASIC3 channels under neutral pH and blocks acid-induced maximal peak current.
价 格：￥电议型 号：T8617产 地：中国大陆
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T7195GSK369796 Dihydrochlorideinhibit,GSK 369796,GSK369796,Inhibitor,GSK369796 Dihydrochloride,GSK-369796
GSK369796 Dihydrochloride,is an anti-malaria drug candidate. is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization(IC50 of 7.5 μM)
价 格：￥电议型 号：T7195产 地：中国大陆
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T22297Clindamycin hydrochloride monohydrate
Clindamycin hydrochloride monohydrate is an oral protein synthesis inhibitory agent that has the ability to suppress the expression of virulence factors in Staphylococcus aureus at sub-inhibitory concentrations (sub-MICs). Clindamycin hydrochloride monohydrate resistance results from enzymatic methylation of the antibiotic binding site in the 50S ribosomal subunit (23S rRNA). Clindamycin hydrochloride monohydrate decreases the production of Panton-Valentine leucocidin (PVL), toxic-shock-staphylo
价 格：￥电议型 号：T22297产 地：中国大陆
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T10896LCSRM617 hydrochloride
CSRM617 hydrochloride is a selective small-molecule inhibitor of the transcription factor ONECUT2 ( OC2, a master regulator of androgen receptor) with a K d of 7.43 uM in SPR assays, directly binds to OC2-HOX domain. CSRM617 hydrochloride induces apoptosis through the appearance of cleaved Caspase-3 and PARP. CSRM617 hydrochloride is well tolerated in the mouse model of prostate cancer [1]
价 格：￥电议型 号：T10896L产 地：中国大陆
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T17227Vernakalant Hydrochloride
Vernakalant Hydrochloride is a mixed voltage- and frequency-dependent Na+ and atria-preferred K+ channel blocker.
价 格：￥电议型 号：T17227产 地：中国大陆
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T10221Abeprazan hydrochloride
Abeprazan hydrochloride is a potassium-competitive acid blocker. It inhibits H+, K+- ATPase by reversible potassium-competitive ionic binding with no acid activation required. It is developed as a potential alternative to a proton pump inhibitor for the treatment of acid-related diseases.
价 格：￥电议型 号：T10221产 地：中国大陆
