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T31603Edeine D；化合物 T31603Edeine D
Edeine D is a bioactive chemical from Bacillus brevis Vm(4).
价 格：￥电议型 号：T31603产 地：中国大陆
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T31602Ecopipam；依考匹泮Sch-39166|||UNII-0X748O646K|||Sch 39166；Sch-39166|||UNII-0X748O646K|||Sch 39166
Ecopipam (UNII-0X748O646K) is a potent, selective and orally active antagonist of dopamine D1/D5 receptor, with Kis of 1.2 nM and 2.0 nM, respectively. Ecopipam shows more than 40-flod selectivity over D2, D4, 5-HT, and α2a receptor (Ki=0.98, 5.52, 0.08, and 0.73 μM, respectively). Ecopipam can be used for the research of schizophrenia and obesity.
价 格：￥电议型 号：T31602产 地：中国大陆
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T31601Eclanamine maleate；化合物 T31601U-48753E|||U48,753E|||U-48,753E|||U48753E|||U 48,753E；U-48753E|||U48,75
Eclanamine was discovered to be slightly mutagenic in the AS52 assay, and a potential agent which was subjected to a battery of short-term assays for genetic activity.
价 格：￥电议型 号：T31601产 地：中国大陆
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T31600Echothiophate Iodide；化合物 T31600Phospholine iodide|||Ecostigmini Sodidum|||Iodide, Echothiophate|||Ec
Echothiophate iodide is an effective long-acting cholinesterase inhibitor for the treatment of glaucoma.
价 格：￥电议型 号：T31600产 地：中国大陆
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T31160Cysteinylcysteine；化合物 T31160Cys-cys；Cys-cys
Cysteinylcysteine is a bioactive chemical.
价 格：￥电议型 号：T31160产 地：中国大陆
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T30160ASMI；化合物 T30160ASMI
ASMI is a cell-permeable cysteine selective, sensitive, and ratiometric fluorescent turn-on probe.
价 格：￥电议型 号：T30160产 地：中国大陆
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T29811AL-16049；化合物 T29811AL 16049|||AL16049；AL 16049|||AL16049
AL-16049 is an FP-Class prostaglandin analog which may be useful in the treatment of glaucoma and ocular hypertension.
价 格：￥电议型 号：T29811产 地：中国大陆
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T29160WNK-IN-3；化合物 T29160WNKIN3；WNKIN3
WNK-IN-3 is a novel allosteric inhibitor of WNK kinase.
价 格：￥电议型 号：T29160产 地：中国大陆
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T29096LVapitadine；伐匹他定R 129160；R 129160
Vapitadine is a non-sedative antihistamine compound that relieves itching caused by atopic dermatitis.
价 格：￥电议型 号：T29096L产 地：中国大陆
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T29096Vapitadine dihydrochloride；伐匹他定盐酸盐Vapitadine 2HCl|||R129160|||R-129160 2HCl|||Vapitadine HCl|||R 129
Vapitadine dihydrochloride(R-129160 2HCl) is a novel, potent, selective and non-sedating compound with inhibitory effects on histamine H1.
价 格：￥电议型 号：T29096产 地：中国大陆
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T28972Tiaramide hydrochloride；化合物Tiaramide hydrochlorideFK-1160|||NTA-194|||FK 1160|||FK1160|||tiaramide；F
Tiaramide hydrochloride (FK-1160) is an anti-inflammatory drug that inhibits the action of mediators released from mast cells and has direct smooth muscle relaxant properties.
价 格：￥电议型 号：T28972产 地：中国大陆
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T28246ONO-1603；化合物 T28246ONO1603；ONO1603
ONO-1603, a prolyl endopeptidase inhibitor, is used potentially for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T28246产 地：中国大陆
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T28181NNC 11-1607；化合物 T28181NNC-11-1607|||NNC11-1607；NNC-11-1607|||NNC11-1607
NNC 11-1607 is a functionally selective agonist of M(1)/M(4) mAChR.
价 格：￥电议型 号：T28181产 地：中国大陆
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T28160Nerispirdine HCl；化合物 T28160HP-184|||HP 184|||Nerispirdine hydrochloride|||HP184；HP-184|||HP 184|||Ne
Nerispirdine is a acetylcholine release enhancer, sodium channel blocker and K(V) 2.1 channel blocker. Nerispirdine inhibits voltage-dependent Na(+) channel currents recorded from human SH-SY5Y cells with an IC(50) of 11.9 micromol/L when measured from a -70 mV holding potential. Nerispirdine also inhibits K(v)1.1 and K(v)1.2 with IC(50) values of 3.6 and 3.7 micromol/L, respectively.
价 格：￥电议型 号：T28160产 地：中国大陆
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T27773LL-739750 2HCl；L-739750盐酸盐L-739750 2HCl(160141-08-2 Free base)；L-739750 2HCl(160141-08-2 Free base)
L-739750 2HCl is a potent inhibitor of peptidomimetic farnesyltransferase, a novel pseudopeptide mimetic with potential anticancer activity.
价 格：￥电议型 号：T27773L产 地：中国大陆
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T27450GSK1482160；化合物 T27450GSK 1482160|||GSK-1482160；GSK 1482160|||GSK-1482160
GSK1482160 is a potent and selective P2X7 receptor allosteric modulator.
价 格：￥电议型 号：T27450产 地：中国大陆
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T26751BBR 2160；化合物 T26751BBR-2160|||BBR2160；BBR-2160|||BBR2160
BBR 2160 is a dihydropyridine derivative belonging to the group of the so-called tiampidine. BBR 2160 has calcium-antagonistic properties in cardiac tissue. Intracellular microelectrodes have been used to characterize the electrophysiological properties of BBR 2160 on guinea-pig papillary muscle and sheep Purkinje fibres. BBR 2160 (10(-7) and 10(-6) M) dose dependently decreased the contractility of driven papillary muscle and Purkinje fibre. This effect was associated with a lowering of the pla
价 格：￥电议型 号：T26751产 地：中国大陆
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T26701AZ12216052；化合物 AZ12216052AZ 12216052|||AZ-12216052；AZ 12216052|||AZ-12216052
AZ12216052 is a GRP8 antagonist with anxiolytic and anti-inflammatory activity and can be used to study obesity and metabolic disorders.
价 格：￥电议型 号：T26701产 地：中国大陆
