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T3067Tideglusib化合物TideglusibNP-12|||NP031112
Tideglusib (NP031112), a non-ATP competitive inhibitor of glycogen synthase kinase 3 (GSK-3), is with anti-inflammatory and neuroprotective activities.
价 格：￥电议型 号：T3067产 地：中国大陆
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T30578BRD3067；化合物 T30578BRD-3067|||BRD 3067；BRD-3067|||BRD 3067
BRD3067 is a negative control for tubastatin A.
价 格：￥电议型 号：T30578产 地：中国大陆
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T30191LAtecegatran TFA；阿特加群三氟乙酸盐Atecegatran TFA(917904-13-3 Free base）|||AR-H067637 TFA；Atecegatran TFA(917
Atecegatran TFA is often used as an anticoagulant and can be used to treat cardiovascular disease.
价 格：￥电议型 号：T30191L产 地：中国大陆
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T30067Aniline, N-ethyl-p-(5-phenylpentyloxy)-, hydrochloride；化合物 T30067Aniline, N-ethyl-p-(5-phenylpentylo
Aniline, N-ethyl-p-(5-phenylpentyloxy)-, hydrochloride is a bioactive chemical.
价 格：￥电议型 号：T30067产 地：中国大陆
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T2968Hyodeoxycholic acid；猪去氧胆酸NSC 60672|||α-Hyodeoxycholic Acid|||HDCA；NSC 60672|||猪去氧胆酸|||α-Hyodeoxychol
Hyodeoxycholic acid (NSC 60672) has been used in trials studying the treatment of Hypercholesterolemia.
价 格：￥电议型 号：T2968产 地：中国大陆
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T29067LUpacicalcet HCl；乌帕西卡塞盐酸盐Upacicalcet HCl(1333218-50-0 Free base)；Upacicalcet HCl(1333218-50-0 Free ba
Upacicalcet HCl is an intravesical calcium mimetic that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on calcium-sensitive receptors in parathyroid cell membranes, thereby lowering PTH levels in the blood.Upacicalcet HCl can be used for the treatment of blood Upacicalcet HCl is a novel compound for the treatment of secondary hyperparathyroidism, targeting amino acid-binding sites of calcium-sensitive receptors. binding sites.
价 格：￥电议型 号：T29067L产 地：中国大陆
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T29067Upacicalcet；乌帕卡塞PLS-240|||SK-1403|||AJT-240；PLS-240|||SK-1403|||AJT-240
Upacicalcet (AJT-240) is an intraventricular calcium mimetic, a SHPT available for human hemodialysis, that inhibits excessive parathyroid hormone (PTH) secretion by directly acting on parathyroid cell membrane calcium-sensitive receptors, thereby lowering blood levels of PTH.Upacicalcet is an orthosteric modulator of calcium-sensitive receptors and prevents adenine-induced secondary vascular calcification and bone disease in a rat model of adenine-induced secondary hyperparathyroidism.
价 格：￥电议型 号：T29067产 地：中国大陆
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T28376PF-06758955 HCl；化合物 T28376PF6758955|||PF 06758955|||PF06758955|||PF 6758955 HCl|||PF-06758955|||PF-6
PF-06758955 is a potent, MAP4K4-selective inhibitor.
价 格：￥电议型 号：T28376产 地：中国大陆
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T28375PF-06745013；化合物 T28375PF6745013|||PF-6745013|||PF 6745013；PF6745013|||PF-6745013|||PF 6745013
PF-06745013 is a potent, MAP4K4-selective inhibitor.
价 格：￥电议型 号：T28375产 地：中国大陆
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T28097MRS1067；化合物 T28097MRS 1067|||MRS-1067；MRS 1067|||MRS-1067
MRS1067 is an antagonist of A3 adenosine receptor.
价 格：￥电议型 号：T28097产 地：中国大陆
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T28067ML372；化合物 T28067ML 372|||ML-372；ML 372|||ML-372
ML372 is a potent and selective SMN Modulator (EC50 = 12 nM, 325% increase inSMN2) with good potency, pharmacokinetics, tolerance, and CNS penetration.
价 格：￥电议型 号：T28067产 地：中国大陆
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T27867LY 106737；化合物 T27867LY106737|||LY-106737；LY106737|||LY-106737
LY 106737 is opioid antagonist in the class of phenylpiperidine.
价 格：￥电议型 号：T27867产 地：中国大陆
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T27678JNJ-39220675；化合物 JNJ-39220675JNJ 39220675|||JNJ39220675；JNJ 39220675|||JNJ39220675
JNJ-39220675 (JNJ 39220675) is a selective and brain permeable histamine H3 receptor antagonist.
价 格：￥电议型 号：T27678产 地：中国大陆
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T27067CP-944629；化合物 T27067CP 944629；CP 944629
CP-944629 is a novel, potent, and selective inhibitor of p38alpha.
价 格：￥电议型 号：T27067产 地：中国大陆
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T26657AR-H067637；化合物 T26657AR-H067637
AR-H067637 is a rapid-binding, reversible and potent (inhibition constant K(i) = 2-4 nM), competitive inhibitor of thrombin, as well as of thrombin bound to fibrin (clot-bound thrombin) or to thrombomodulin. The total amount of free thrombin generated in platelet-poor clotting plasma was inhibited concentration-dependently by AR-H067637, with a concentration giving half maximal inhibition (IC(50)) of 0.6 microM. AR-H067637 also inhibited thrombin-induced platelet activation (by glycoprotein IIb/
价 格：￥电议型 号：T26657产 地：中国大陆
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T26530ABT-472；化合物 T26530A-620223 (HCl salt)|||AKOS016845980|||DTXSID70670431；A-620223 (HCl salt)|||AKOS016
ABT-472 is a novel PARP inhibitor
价 格：￥电议型 号：T26530产 地：中国大陆
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T26190SK&F 106760；化合物 T26190SK&|||F-106760|||SKF 106760|||SKF-106760|||F106760|||SKF106760|||F 1067
SKF 106760 is used as a glycoprotein IIb/IIIa antagonist.
价 格：￥电议型 号：T26190产 地：中国大陆
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T26067Rev 6207；化合物 T26067Rev-6207；Rev-6207
Rev 6207 is a non-sulfhydryl ACE-inhibitor.
价 格：￥电议型 号：T26067产 地：中国大陆
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T25764LY 81067；化合物 T25764Lilly-81067|||LY81067|||Lilly81067|||Lilly 81067|||LY-81067；Lilly-81067|||LY81067
LY 81067 is a new anticonvulsive compound that effectively protects against pentylenetetrazole- and picrotoxin-induced convulsions in mice. It exerts its anticonvulsant effects by binding to or near picrotoxin binding sites.
价 格：￥电议型 号：T25764产 地：中国大陆
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T25459GR 100679；化合物 T25459GR100679|||GR-100679；GR100679|||GR-100679
GR 100679 is an antagonist of NK2 receptor.
价 格：￥电议型 号：T25459产 地：中国大陆
