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T13437(R,R)-Palonosetron Hydrochloride；(R,R)-盐酸帕洛诺司琼(R,R)-Palonosetron Hydrochloride
(R,R)-Palonosetron Hydrochloride is the active enantiomer of Palonosetron
价 格：￥电议型 号：T13437产 地：中国大陆
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T13425(1S,3R,5R)-PIM447 dihydrochloride；化合物 T13425(1S,3R,5R)-LGH447 dihydrochloride；(1S,3R,5R)-LGH447 dihy
(1S,3R,5R)-PIM447 (dihydrochloride) an inhibitor of PIM(IC50 of 0.095 μM for Pim1, 0.522 μM for Pim2 and 0.369 μM for Pim3).
价 格：￥电议型 号：T13425产 地：中国大陆
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T13423(1R,2R)-2-PCCA hydrochloride；(1R,2R)-2-PCCA盐酸盐(1R,2R)-2-PCCA(hydrochloride)；(1R,2R)-2-PCCA(hydrochlo
(1R,2R)-2-PCCA hydrochloride is a potent, selective, and blood-brain-barrier-crossing GPR88 receptor agonist with an EC50 value of 1140 n in striatal membranes of WT mice.(1R,2R)-2-PCCA hydrochloride can be used to study the central nervous system.
价 格：￥电议型 号：T13423产 地：中国大陆
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T13421(-)-Cevimeline hydrochloride hemihydrate；化合物 T13421(-)-SNI-2011|||(-)-AF102B hydrochloride hemihydra
Cevimeline hydrochloride hemihydrate ((-)-SNI-2011), a novel muscarinic receptor agonist, is being explored as a potential treatment for xerostomia in Sjogren´s syndrome, exhibiting an IC50 value indicative of its affinity for mAChR. This compound´s pharmacological effects on the gastrointestinal, urinary, and reproductive systems, alongside its impact on various tissues, were thoroughly examined in species including mice, rats, guinea pigs, rabbits, and dogs. The metabolic breakdown
价 格：￥电议型 号：T13421产 地：中国大陆
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T1341LNortropine Hydrochloride；化合物 T1341LNortropine Hydrochloride
Nortropine Hydrochloride is a secondary metabolite of tropine derivative drugs.
价 格：￥电议型 号：T1341L产 地：中国大陆
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T13414ZT 52656A hydrochloride；化合物ZT 52656A hydrochlorideZT 52656A hydrochloride
ZT 52656A is a selective agonist of kappa opioid, and used for the prevention or alleviation of pain in the eye.
价 格：￥电议型 号：T13414产 地：中国大陆
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T13413Zoniporide hydrochloride hydrate；化合物 T13413CP-597396 hydrochloride hydrate；CP-597396 hydrochloride h
Zoniporide hydrochloride hydrate is a potent and selective sodium-hydrogen exchanger type 1 (NHE-1) inhibitor. Zoniporide hydrochloride hydrate inhibits human NHE-1 with IC50 of 14 nM.
价 格：￥电议型 号：T13413产 地：中国大陆
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T13412LZM223 hydrochloride (2031177-48-5 free base)；化合物 T13412LZM223 hydrochloride；ZM223 hydrochloride
ZM223 hydrochloride is an orally active, potent non-covalent inhibitor of NEDD8 activating enzyme (NAE), and with excellent anticancer activity.
价 格：￥电议型 号：T13412L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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T13403ZK-90055 hydrochloride；化合物ZK-90055盐酸盐ZK 90055 hydrochloride|||ZK90055 hydrochloride；ZK 90055 hydroch
ZK-90055 hydrochloride is a β2 adrenergic receptor agonist used to study asthma.
价 格：￥电议型 号：T13403产 地：中国大陆
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T13390ZD 7155 hydrochloride；ZD 7155盐酸盐ZD 7155 hydrochloride
ZD 7155 hydrochloride is an angiotensin II receptor type 1 (AT1 receptor) antagonist.
价 格：￥电议型 号：T13390产 地：中国大陆
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T13387LZatebradine hydrochloride；扎替雷定盐酸盐UL-FS-49CL|||UL-FS-49；UL-FS-49CL|||UL-FS-49
Zatebradine hydrochloride (UL-FS-49CL) is a highly effective and effective HCN Channel inhibitor (IC50:1.96 ?M). HCN Channel is an effective hyperpolarization activated loop nucleotide gated channel. Zatebradine hydrochloride blocks slow inward currents through human HCN1, HCN2, HCN3, and HCN4 channels with IC50 values of 1.83 ?M, 2.21 ?M, 1.90 ?M, and 1.88 ?M, respectively.
价 格：￥电议型 号：T13387L产 地：中国大陆
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T13384LY-33075 dihydrochloride；化合物Y-33075 dihydrochlorideY-33075 dihydrochloride
Y-33075 dihydrochloride is a selective inhibitor of ROCK(IC50 of 3.6 nM).
价 格：￥电议型 号：T13384L产 地：中国大陆
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T13372YM-58790 hydrochloride；化合物 T13372YM-58790 hydrochloride
YM-58790 hydrochloride is a potent M3 muscarinic receptor antagonist(Ki of 15 nM).
价 格：￥电议型 号：T13372产 地：中国大陆
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T13337WEHI-539 hydrochloride；化合物 T13337WEHI-539 hydrochloride
WEHI-539 hydrochloride is a selective Bcl-XL inhibitor (IC50: 1.1 nM).
价 格：￥电议型 号：T13337产 地：中国大陆
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T13330WAY-213613 hydrochloride；化合物WAY-213613 hydrochlorideWAY-213613 hydrochloride (868359-05-1 free base)
WAY-213613 hydrochloride is a potent, selective nonsubstrate reuptake inhibitor of GLT-1/EAAT2 with IC 50 of 85 nM. WAY-213613 hydrochloride inhibits EAAT1 and EAAT3 with IC50 values of 5 and 3.8 microM, respectively. WAY-213613 hydrochloride shows no activity at ionotropic and metabotropic glutamate receptors. It is a potential tool for the elucidation of EAAT2 function and can be used for the research of central nervous system [1] [2].
价 格：￥电议型 号：T13330产 地：中国大陆
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T13329LVofopitant dihydrochloride沃弗呲坦盐酸盐GR 205171A|||Vofopitant 2HCl
Vofopitant dihydrochloride (GR 205171A) is an orally available, selective tachykinin NK1 receptor antagonist that inhibits [3H]SP binding to NK1 with pKi values of 9.5 and 10.6, respectively.Vofopitant dihydrochloride is a potential compound for the treatment of pathological vomiting. Vofopitant dihydrochloride is a potential compound for the treatment of pathological vomiting.
价 格：￥电议型 号：T13329L产 地：中国大陆
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T13328AE0047 Hydrochloride；化合物 T13328AE0047 Hydrochloride
AE0047 Hydrochloride is a blocker of calcium, and used in the research of the hypertensive disease.
价 格：￥电议型 号：T13328产 地：中国大陆
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T13320VU591 hydrochloride；化合物VU591 hydrochlorideVU591 hydrochloride
VU591 hydrochloride is a selective renal outer medullary potassium channel (Kir1.1, ROMK) antagonist (IC50：0.24 μM). Thought to block the intracellular pore of the Kir1.1 channel. Exhibits no effect on Kir7.1 at concentrations up to 10 μM; does not inhibit Kir2.1, Kir2.3 or Kir4.1. Displays similar potency to VU 590
价 格：￥电议型 号：T13320产 地：中国大陆
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T13317VU0364770 hydrochloride；化合物 T13317VU0364770 hydrochloride
VU0364770 hydrochloride is a potent and selective mGlu4 positive allosteric modulator (PAM) (EC50s: 290 nM and 1.1 μM at rat mGlu4 and human mGlu4 receptor, respectively).
价 格：￥电议型 号：T13317产 地：中国大陆
