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T6225Adenine hydrochloride腺嘌呤盐酸盐；Adenine HCl；6-Aminopurine hydrochloride
Adenine HCl is a hydrochloride salt form of adenine which is a nucleobase with a variety of roles in biochemistry.
价 格：￥电议型 号：T6225产 地：中国大陆
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T6221Nalmefene hydrochlorideNalmefene HCl
Nalmefene antagonizes the effects of opioids by competing for the opioid receptors in the CNS.
价 格：￥电议型 号：T6221产 地：中国大陆
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T6175ADL-5859ADL5859 HCl；ADL5859 Hydrochloride
ADL5859 HCl is a selective δ-opioid receptor agonist ( Ki: 0.8 nM), selectivity against opioid receptor κ, μ, and little inhibition for the hERG channel.
价 格：￥电议型 号：T6175产 地：中国大陆
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T6162BS-181 hydrochlorideBS-181 HCl
BS-181 HCl is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.
价 格：￥电议型 号：T6162产 地：中国大陆
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T6161Tubastatin A HydrochlorideTubastatin A HCl；TSA HCl
Tubastatin A HCl is an effective and specific HDAC6 inhibitor (IC50: 15 nM). It has selectivity (>1000-fold) against all other isozymes except HDAC8 (>57-fold).
价 格：￥电议型 号：T6161产 地：中国大陆
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T6158LDN-193189 HClLDN193189 Hydrochloride
LDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
价 格：￥电议型 号：T6158产 地：中国大陆
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T6145ZM39923 hydrochlorideZM 39923 HCl；JAK3 Inhibitor IV
ZM 39923 HCl is an JAK1/3 inhibitor with pIC50 of 4.4/7.1, almost no activity to JAK2 and modestly potent to EGFR; also found to be sensitive to transglutaminase.
价 格：￥电议型 号：T6145产 地：中国大陆
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T6139LA-674563 2HCl(552325-73-2(fb-2hcl))
A-674563 is an Akt1 inhibitor with Ki of 11 nM, modest potent to PKA and >30-fold selective for Akt1 over PKC.
价 格：￥电议型 号：T6139L产 地：中国大陆
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T6069Gemcitabine hydrochlorideLY 188011 hydrochloride；LY188011；Gemzar；Gemcitabine HCl；吉西他滨盐酸盐；盐酸吉西他滨
Gemcitabine is a DNA synthesis inhibitor (IC50s: 12, 18, 40, 92.7, 89.3 in Capan2, BxPC-3, Mia Paca-2, PANC-1, and PL-45 cells, respectively).
价 格：￥电议型 号：T6069产 地：中国大陆
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T6018Zosuquidar trihydrochloride唑喹达三盐酸盐；RS 33295-198 (D06387) 3HCl；Zosuquidar (LY335979) 3HCl；LY-335979 t
Zosuquidar (LY335979) is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM. Phase 3.
价 格：￥电议型 号：T6018产 地：中国大陆
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T6010Idarubicin hydrochlorideZavedos；Idarubicin HCl；4-demethoxydaunorubicin (NSC256439, 4-DMDR) HCl；Idamy
Idarubicin HCl, a hydrochloride salt form of Idarubicin, is a DNA topoisomerase II (topo II) inhibitor for MCF-7 cells ( IC50: 3.3 ng/mL).
价 格：￥电议型 号：T6010产 地：中国大陆
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T6004Tetrahydropapaverine hydrochloride四氢罂粟碱盐酸盐；Tetrahydropapaverine HCl；Norlaudanosine HCl；Tetrahydroalk
Tetrahydropapaverine, an analogue of salsolinol and tetrahydropapaveroline, has neurotoxicity on dopamine neurons.
价 格：￥电议型 号：T6004产 地：中国大陆
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T5833CC-401 HydrochlorideCC401 HCl
CC-401 is a second generation ATP-competitive anthrapyrazolone c-Jun N terminal kinase (JNK) inhibitor (Ki of 25 to 50 nM.)with potential antineoplastic activity.
价 格：￥电议型 号：T5833产 地：中国大陆
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T5817PKC-theta inhibitor hclPKC-theta inhibitor
PKC-theta inhibitor is a selective PKC-θinhibitor(IC50:12 nM).
价 格：￥电议型 号：T5817产 地：中国大陆
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T56722,4-Diaminophenoxyethanol HCl
Isophorone (3,5,5-trimethyl-2-cyclohexen-1-one), a monoterpene, and the structurally related 1,8-cineole and camphor, have demonstrated a protective effect against cancer, biological activity against a variety of microorganisms, and anti-oxidant propertie
价 格：￥电议型 号：T5672产 地：中国大陆
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T5398BMS 599626 2HCl (873837-23-1(HCl))AC480 dihydrochloride
BMS-599626 (AC480) is a selective inhibitor of HER1 and HER2 (IC50s: 20 nM and 30 nM), ~8-fold less potent to HER4, >100-fold to Lck, VEGFR2, c-Kit, MET, etc.
价 格：￥电议型 号：T5398产 地：中国大陆
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T5356MRT68921 HCl盐酸MRT68921
MRT68921 hydrochloride is a potent inhibitor of both ULK1 and ULK2 (IC50s: 2.9 and 1.1 nM, respectively).
价 格：￥电议型 号：T5356产 地：中国大陆
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T5196DIM-C-pPhCO2Me
DIM-C-pPhCO2Me is a nuclear receptor 4A1 (NR4A1) antagonist.
价 格：￥电议型 号：T5196产 地：中国大陆
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T5162MRT67307 HCl (1190378-57-4(free base))盐酸MRT67307
MRT67307 is a kinase inhibitor of TBK1, MARK1-4, IKKε, and NUAK1 (IC50: 19, 27-52, 160, and 230 nM, respectively).
价 格：￥电议型 号：T5162产 地：中国大陆
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T5128RGX-104 hydrochlorideSB742881；RGX-104 HCl；盐酸RGX-104
RGX-104 is a liver X receptor (LXR) agonist with potential immunomodulating and antineoplastic activities. It modulates innate immunity via transcriptional activation of the ApoE gene.
价 格：￥电议型 号：T5128产 地：中国大陆
