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T23672AH-1058 HCl；化合物 T23672AH 1058 HCl；AH 1058 HCl
AH-1058 HCl is a lipophilic antiarrhythmic calcium channel blocker.
价 格：￥电议型 号：T23672产 地：中国大陆
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T23653Afegostat HCl；化合物 T23653Afegostat|||AT-2101|||Afegostat hydrochloride|||AT2101；Afegostat|||AT-2101||
Afegostat is an acid β-glucosidase (GCase) active site inhibitor that acts as a pharmacological chaperone. Afegostat inhibits GCase with K(i) ~30 nM for wild-type and mutant enzymes. Afegostat was an experimental drug for the treatment of certain forms of Gaucher´s disease.
价 格：￥电议型 号：T23653产 地：中国大陆
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T23642LADR-851 HCl；化合物 T23642LAdr-851|||Adr 851|||Adr851；Adr-851|||Adr 851|||Adr851
ADR-851 HCl is an HT3 receptor antagonist. It works against mechanical, acute thermal, and formalin-induced inflammatory pain.
价 格：￥电议型 号：T23642L产 地：中国大陆
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T23622Acorafloxacin HCl；化合物 T23622JNJ-32729463|||JNJ-Q2 hydrochloride|||Acorafloxacin hydrochloride|||JNJ
Acorafloxacin is a broad-spectrum fluoroquinolone antibacterial drug being developed for the treatment of acute bacterial skin and skin structure infections and community-acquired pneumonia.
价 格：￥电议型 号：T23622产 地：中国大陆
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T23619LAcodazole hydrochloride；化合物 T23619LNSC 305884|||NSC305884|||Acodazole HCl|||NSC-305884；NSC 305884|||
Acodazole hydrochloride is a synthetic imidazoquinoline. It also has antineoplastic activity. Acodazole intercalates into DNA, cause disruption of DNA replication.
价 格：￥电议型 号：T23619L产 地：中国大陆
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T23529WAY 316606 HCl (915759-45-4 free base)；化合物 T23529WAY 316606 HCl；WAY 316606 HCl
WAY 316606 HCl is a selective small-molecule inhibitor of secreted frizzled-related protein-1 (EC50: 0.65 μM).
价 格：￥电议型 号：T23529产 地：中国大陆
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T23523W-5 hydrochloride；盐酸W-5W-5 HCl|||W 5 (hydrochloride)|||N-(6-Aminohexyl)-1-naphthalenesulfonamide HCl
W-5 hydrochloride (N-(6-Aminohexyl)-1-naphthalenesulfonamide HCl) is a potent calmodulin antagonist.
价 格：￥电议型 号：T23523产 地：中国大陆
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T23522W-13 hydrochloride；化合物W-13盐酸盐W-13 HCl；W-13 HCl
W-13 hydrochloride (W-13 HCl) is a calmodulin antagonist.
价 格：￥电议型 号：T23522产 地：中国大陆
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T23512VU 0364739 hydrochloride；VU 0364739 盐酸盐VU 0364739 HCl；VU 0364739 HCl
VU 0364739 hydrochloride (VU 0364739 HCl) is a selective and potent inhibitor of phospholipase D2 (PLD2) with IC50s of 20 and 1500 nM for PLD2 and PLD1, respectively.VU 0364739 hydrochloride exhibits potential anticancer activity and induces apoptosis. VU 0364739 hydrochloride has potential anticancer activity, induces apoptosis, and can be used in the study of cancer and metabolic-related diseases.
价 格：￥电议型 号：T23512产 地：中国大陆
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T23451Tedizolid HCl (856866-72-3 free base)；化合物 T23451Tedizolid HCl；Tedizolid HCl
Tedizolid HCl is a reversible, novel oxazolidinone antibiotic (IC50: for MAO-A (monoamine oxidase-A), 8.7 uM; for MAO-B, 5.7 uM). It is the first oxazolidinone to be approved since linezolid in 2000. Tedizolid phosphate is the second commercially available oxazolidinone antibiotic and is the prodrug form of tedizolid with a fixed once-daily dose. As an expanded-spectrum oxazolidinone, it has potent activity against a wide range of Gram-positive pathogens.
价 格：￥电议型 号：T23451产 地：中国大陆
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T23418Tandutinib (MLN518) HCl；化合物 T23418Tandutinib (MLN518) HCl
Tandutinib is an effective antagonist for FLT3, platelet-derived growth factor receptor (PDGFR), and c-Kit. Tandutinib potently inhibited the activity of FLT3, PDGFR, and c-Kit (IC50: ~200 nM).
价 格：￥电议型 号：T23418产 地：中国大陆
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T23337SCH772984 HCl；化合物SCH772984 HClSCH772984 HCl
SCH772984 HCl is a selective inhibitor of ERK1/2 that displays behaviors of both type I and type II kinase inhibitors, with IC50s of 4 and 1 nM, respectively. SCH772984 HCl has nanomolar cellular potency in tumor cells with mutations in BRAF, NRAS, or KRA
价 格：￥电议型 号：T23337产 地：中国大陆
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T2330LRilpivirine HCl化合物 T2330LRilpivirine hydrochloride|||TMC278|||Rilpivirine|||TMC-278|||TMC 278. trade
Rilpivirine is a potent non-nucleoside reverse transcriptase inhibitor.
价 格：￥电议型 号：T2330L产 地：中国大陆
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T23288L(S)-3,4-DCPG HCl；(S)-3,4-DCPG 盐酸盐(S)-3,4-Dicarboxyphenylglycine HCl|||(S)-3,4-DCPG HCl(201730-11-2 F
(S)-3,4-DCPG HCl ((S)-3,4-Dicarboxyphenylglycine HCl) is a selective metabotropic glutamate receptor 8a (mGluR8a) agonist that has an effect on human mGluR8-expressing AV12-664 cells with an EC50 of 31 nM.
价 格：￥电议型 号：T23288L产 地：中国大陆
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T23265RS 67333 hydrochloride；盐酸RS67333RS 67333 (hydrochloride)|||RS 67333 HCl；RS 67333 (hydrochloride)|||R
RS 67333 hydrochloride (RO5203648) is a potent, selective partial agonist of the 5-HT4 receptor (5-HT4R) with a pKi value of 8.7 in guinea-pig striatum. It demonstrates lower binding affinities for other receptors, including 5-HT1A, 5-HT1D, 5-HT2A, 5-HT2C, dopamine D1 and D2, and muscarinic M1-M3 receptors. Notably, RS 67333 hydrochloride exhibits neuroprotective properties, rendering it useful in Alzheimer´s disease research.
价 格：￥电议型 号：T23265产 地：中国大陆
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T23215L(R)-3,4-DCPG HCl；(R)-3,4-DCPG 盐酸盐(R)-3,4-DCPG HCl(201730-10-1 Free base)；(R)-3,4-DCPG HCl(201730-10-
(R)-3,4-DCPG HCl is a potent and selective mGlu8a receptor agonist that activates metabotropic glutamate receptors on primary afferent terminals in the neonatal rat spinal cord.
价 格：￥电议型 号：T23215L产 地：中国大陆
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T2319Acotiamide monohydrochloride trihydrate盐酸阿考替胺Acotiamide hydrochloride|||YM-443 HCl|||盐酸阿考替胺|||Z-338
Acotiamide monohydrochloride trihydrate (Z-338 HCl) is the hydrochloride salt form of acotiamide, a prokinetic agent with gastrointestinal (GI) motility-enhancing activity. Although the exact mechanism by which acotiamide exerts its effect has yet to be fully elucidated, this agent appears to inhibit acetylcholinesterase (AchE), an enzyme responsible for the breakdown of acetylcholine (Ach). Increased Ach concentrations lead to an improvement of gastric emptying and GI motility and eventually to
价 格：￥电议型 号：T2319产 地：中国大陆
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T2315GSK-LSD1 dihydrochloride；化合物GSK-LSD1 dihydrochlorideGSK-LSD1 (hydrochloride)|||GSK-LSD1 2HCl；GSK-LSD
GSK-LSD1 dihydrochloride (GSK-LSD1 2HCl) is a specificity irreversible LSD1 inhibitor (IC50: 16 nM). The selectivity of GSK-LSD1 for LSD1 is >1000 fold over other closely related FAD utilizing enzymes (i.e. MAO-A, LSD2, MAO-B).
价 格：￥电议型 号：T2315产 地：中国大陆
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T23149Phenyl-benzothiazole HCl (92-36-4 free base)；化合物 T23149Phenyl-benzothiazole HCl；Phenyl-benzothiazole
An azole for proteomics research
价 格：￥电议型 号：T23149产 地：中国大陆
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T23143PG 01037 dihydrochloride；PG01037盐酸盐PG-01037 2HCl；PG-01037 2HCl
PG 01037 dihydrochloride (PG-01037 2HCl) is a potent and selective dopamine D3 receptor antagonist with a Ki of 0.7 nM.
价 格：￥电议型 号：T23143产 地：中国大陆
