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T12398515,16-Dihydrotanshindiol C；化合物 15,16-Dihydrotanshindiol C15,16-Dihydrotanshindiol C
15,16-Dihydrotanshindiol C is a useful organic compound for research related to life sciences and the catalog number is T123985.
价 格：￥电议型 号：T123985产 地：中国大陆
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T12382PD-159020；化合物 T12382PD-159020
PD-159020 is a non-selective antagonist of ETA/ETB(hETA and hETB with IC50s of 30 and 50 nM , respectively).
价 格：￥电议型 号：T12382产 地：中国大陆
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T123815Populin；化合物 PopulinPopulin
Populin is a useful organic compound for research related to life sciences. The catalog number is T123815 and the CAS number is 99-17-2.
价 格：￥电议型 号：T123815产 地：中国大陆
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T12323ORM-15341；ORM-15341ORM-15341
ORM-15341 is a potent and full antagonist for human AR (hAR)( with IC50 values of 38 nM as shown by transactivation assays in AR-HEK293 cells)
价 格：￥电议型 号：T12323产 地：中国大陆
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T12315OR-1896化合物 OR-1896OR 1896|||OR1896
OR-1896 is the active metabolite of Levosimendan, a highly specific phosphodiesterase (PDE III) inhibitor, a vasodilator with partial anti-inflammatory properties that produces vasodilation in different types of blood vessels through activation of ATP-sensitive (KATP) and other potassium channels.OR-1896 can be used to study heart failure and vascular dysfunction. OR-1896 can be used to study heart failure and vascular dysfunction.
价 格：￥电议型 号：T12315产 地：中国大陆
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T12245Nosantine racemate；诺次黄嘌呤外消旋体NPT-15392 racemate；诺次黄嘌呤外消旋体|||NPT-15392 racemate
Nosantine racemate is the racemate of Nosantine which is a IL-2 inducer or enhancer of IL-2 induction by phytohemagglutinin (PHA).
价 格：￥电议型 号：T12245产 地：中国大陆
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T12237NMS-P715；化合物NMS-P715NMS-P715
NMS-P715 is a highly selective and ATP-competitive MPS1 inhibitor(IC50 of 182 nM).
价 格：￥电议型 号：T12237产 地：中国大陆
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T12215Nexopamil racemate；奈索帕米外消旋体(Rac)-Nexopamil；(Rac)-Nexopamil
Nexopamil racemate（(Rac)-Nexopamil） is a racemate of Nexopamil. The Nexopamil racemate has potential anti-asthmatic and anti-ulcer activity.
价 格：￥电议型 号：T12215产 地：中国大陆
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T12208Nepafenac-d5；奈帕芬胺 D5AHR-9434 D5|||AL-6515 D5；奈帕芬胺 D5|||AHR-9434 D5|||AL-6515 D5
Nepafenac D5 is the deuterium labeled Nepafenac, which is a selective inhibitor of COX-2 .
价 格：￥电议型 号：T12208产 地：中国大陆
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T12159APNEA；N6-[2-(4-氨基苯基)乙基]腺嘌呤(2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymeth
APNEA ((2R,3R,4S,5R)-2-[6-[2-(4-aminophenyl)ethylamino]purin-9-yl]-5-(hydroxymethyl)oxolane-3,4-diol) is a non-selective agonist of adenosine A3 receptor.
价 格：￥电议型 号：T12159产 地：中国大陆
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T12158N3PT化合物 T12158N3-pyridyl thiamine
N3PT is a potent and selective inhibitor of transketolase(TK) with IC50 of 22 nM for Apo-TK)
价 格：￥电议型 号：T12158产 地：中国大陆
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T12157ETA antagonist 1；化合物 T12157ETA antagonist 1
ETA antagonist 1 is an antagonist of ETA selective (IC50 of 0.08 μM).
价 格：￥电议型 号：T12157产 地：中国大陆
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T12155Y1 receptor antagonist 1；Y1 receptor 拮抗剂 1H 409-22 isomer；H 409-22 isomer
Y1 receptor antagonist 1 (H 409-22 isomer) is the active isomer of H-409/22, a neuropeptide Y (NPY) Y1 receptor antagonist that dose-dependently antagonizes the vascular response to exogenous and endogenous NPY in pigs. lagodeoxycholic acid (H 409-22 isomer) is the active isomer of H-409/22, an antagonist of neuropeptide Y (NPY) Y1 receptor.
价 格：￥电议型 号：T12155产 地：中国大陆
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T12154LN-Desethyl amodiaquine dihydrochloride；去乙基阿莫地喹盐酸盐N-Desethyl amodiaquine dihydrochloride
N-Desethyl amodiaquine dihydrochloride is an antiparasitic agent and the major biologically active amodiaquine metabolite. Its IC50 values against strains V1/S and 3D7 were 97 nM and 25 nM, respectively.
价 格：￥电议型 号：T12154L产 地：中国大陆
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T12154N-Desethyl amodiaquine；去乙基阿莫地喹N-Desethyl amodiaquine
N-Desethyl amodiaquine is an antiparasitic agent and the major bioactive amodiaquine metabolite. Its IC50 values against strains V1/S and 3D7 were 97 nM and 25 nM, respectively.
价 格：￥电议型 号：T12154产 地：中国大陆
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T12153N-type calcium channel blocker-1；化合物 T12153N-type calcium channel blocker-1
N-type calcium channel blocker-1 is an orally active analgesic agent,shows high affinity to functionally block N-type calcium channels.
价 格：￥电议型 号：T12153产 地：中国大陆
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T12152N-piperidine Ibrutinib hydrochloride；N-piperidine Ibrutinib 盐酸盐N-piperidine Ibrutinib hydrochloride
N-piperidine Ibrutinib hydrochloride is a potent BTK inhibitor, a BTK ligand, inhibits WT BTK and C481S BTK, which can be used to synthesize a range of PROTAC molecules.N-piperidine Ibrutinib hydrochloride has potential anticancer N-piperidine Ibrutinib hydrochloride has potential anticancer activity, inhibiting the growth and proliferation of cancer cells.
价 格：￥电议型 号：T12152产 地：中国大陆
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T12151N-Methylmoranoline；化合物 T12151MOR 14|||N-Methyl-1-deoxynojirimycin|||N-Methylmoranolin；MOR 14|||N-Met
N-Methylmoranoline is an inhibitor of α-glucosidase.
价 格：￥电议型 号：T12151产 地：中国大陆
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T12150N-Methylbenzamide；N-甲基苯甲酰胺N-Methylbenzamide
N-Methylbenzamide is a potent phosphodiesterase 10A (PDE10A) inhibitor,with anti-cancer activity.
价 格：￥电议型 号：T12150产 地：中国大陆
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T1215Nicardipine hydrochloride；盐酸尼卡地平RS-69216|||Nicardipine HCl|||YC-93 Hydrochloride；盐酸尼卡地平|||RS-69216||
Nicardipine hydrochloride (YC-93 Hydrochloride) is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contraction of coronary and peripheral arteries, resulting in lowered oxygen requirements for heart muscle and decreased arterial contraction and spasm. It is used clinically as a cerebral and coronary vasodilator.
价 格：￥电议型 号：T1215产 地：中国大陆
