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T29225ZK118182 isopropyl ester；化合物 T29225ZK118182|||ZK 118182|||ZK-118182；ZK118182|||ZK 118182|||ZK-118182
ZK118182 isopropyl ester is a PG analog with potent DP-agonist activity (EC50 = 16.5 nM) and high affinity for the DP receptor (Ki = 74 nM).
价 格：￥电议型 号：T29225产 地：中国大陆
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T29224ZK112993；化合物 T29224ZK-112993|||ZK 112993；ZK-112993|||ZK 112993
ZK112993 is an antagonist of human progesterone receptor.
价 格：￥电议型 号：T29224产 地：中国大陆
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T29223ZK110841；化合物 T29223ZK-110841|||ZK 110841；ZK-110841|||ZK 110841
ZK110841 is an agonist of prostaglandin DP-receptors on human platelet. ZK110841 elevated the cyclic AMP level in EBTr cells dose-dependently, being more than 100 fold over the basal level at 1 microM.
价 格：￥电议型 号：T29223产 地：中国大陆
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T29203Zanapezil fumarate；化合物 T29203TAK 147|||TAK147|||TAK-147；TAK 147|||TAK147|||TAK-147
Zanapezil is an acetylcholinesterase (AChE) inhibitor. Zanapezil increases choline acetyltransferase activity in cultured rat septal cholinergic neurons.
价 格：￥电议型 号：T29203产 地：中国大陆
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T29087VA-K-14 hydrochloride；VA-K-14盐酸盐VAK14 Hydrochloride|||VA K 14 HCl|||VA-K-14 HCl|||VAK14 HCl；VAK14 Hy
VA-K-14 hydrochloride（VAK14 HCl） is a selective thyrotropin receptor (TSHR) antagonist (IC50= 12.3 μM) that inhibits TSHR stimulation by serum and monoclonal TSHR-stimulating antibodies from patients with GD and abrogates TSHR signaling.
价 格：￥电议型 号：T29087产 地：中国大陆
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T29051UK-122 TFA salt；化合物 T29051UK122|||uPA Inhibitor II|||UK122 TFA salt|||UK 122|||UK-122|||K122 triflor
UK-122 is a potent and selective uPA inhibitor (Ki = 20 nM). The IC(50) of UK122 in a cell-free indirect uPA assay is 0.2 micromol/L. UK122 showed little cytotoxicity against CFPAC-1 cells (IC(50) > 100 micromol/L) but significantly inhibited the migration and invasion of this pancreatic cancer cell line.
价 格：￥电议型 号：T29051产 地：中国大陆
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T28983TLK19781；化合物 T28983TLK 19781|||TLK-19781；TLK 19781|||TLK-19781
TLK19781 is an insulin receptor modulator.
价 格：￥电议型 号：T28983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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T28914Tak 187；化合物 T28914Tak-187|||Tak187；Tak-187|||Tak187
Tak 187 is a long-lasting inhibitor of ergosterol biosynthesis.
价 格：￥电议型 号：T28914产 地：中国大陆
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T28652S6K1-IN-DG2；S6K1抑制剂DG2S6K1 Inhibitor DG2|||S6K1-Inhibitor-DG2|||S6K1 IN DG2|||S6K1INDG2|||S6K1Inhibi
S6K1-IN-DG2(S6K1InhibitorDG2) is a potent p70S6K inhibitor with an IC50 value of less than 100 nM.
价 格：￥电议型 号：T28652产 地：中国大陆
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T28416PIK-108；化合物PIK-108PIK 108|||PIK108；PIK 108|||PIK108
PIK-108 is an allosteric inhibitor of phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunits β and δ (PI3Kβ/δ).
价 格：￥电议型 号：T28416产 地：中国大陆
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T28129Naltalimide；化合物 T28129TRK-130|||TRK 130|||TRK130；TRK-130|||TRK 130|||TRK130
Naltalimide is a unique ?-opioid receptor partial agonist. Naltalimide also enhances the bladder storage function by modulating the afferent limb of the micturition reflex through ?-opioid receptors in the spinal cord.
价 格：￥电议型 号：T28129产 地：中国大陆
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T28054MK181；化合物 T28054MK 181|||MK-181；MK 181|||MK-181
MK181 is an inhibitor of AKR1B10, a tumor marker and promising antineoplastic target.
价 格：￥电议型 号：T28054产 地：中国大陆
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T27832Lifibrol；利弗布罗U 83860|||K-12148|||K-12.148|||U-83860|||K12148；U 83860|||K-12148|||K-12.148|||U-83860|
Lifibrol (U-83860) is an inhibitor of cholesterol synthesis.Lifibrol has anticholesterol and hypolipidemic properties and promotes the conversion of LDL Apo B-100 in patients with hypercholesterolemia and mixed hyperlipidemia.
价 格：￥电议型 号：T27832产 地：中国大陆
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T27751KSK-120；化合物 T27751KSK120|||KSK 120；KSK120|||KSK 120
KSK-120 is a potent Chlamydia trachomatis inhibitor, it targets the glucose-6-phosphate (G-6P) metabolism pathway of Chlamydia trachomatis.
价 格：￥电议型 号：T27751产 地：中国大陆
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T27743KRH-594 free acid；化合物 T27743WK14922K|||WK-1492|||WK-14922K|||WK1492；WK14922K|||WK-1492|||WK-14922K||
KRH-594 is a potent, specific and insurmountable AT1 receptor antagonist. KRH-594 ameliorates hyperlipidaemia and nephropathy in diabetic spontaneously hypertensive rats. KRH-594 prevents end-organ damage in stroke-prone spontaneously hypertensive/Izm rats.
价 格：￥电议型 号：T27743产 地：中国大陆
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T27707K118；化合物 T27707K 118|||K-118；K 118|||K-118
K118 is an inhibitor of SH2-containing inositol 5´ phosphatase 1 (SHIP1). It reverses diet- and age-associated obesity and metabolic syndrome.
价 格：￥电议型 号：T27707产 地：中国大陆
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T27706K-111；化合物 K-111BM 170744|||K111|||K 111|||BM170744|||BM-170744；BM 170744|||K111|||K 111|||BM170744||
K-111 (BM-170744) is an orally available peroxisome proliferator-activated receptor (PPAR)-alpha agonist and insulin enhancer for the study of obesity-type diabetes mellitus and the metabolic syndrome.
价 格：￥电议型 号：T27706产 地：中国大陆
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T27705K103 Hydrochloride；化合物 T27705K103|||K-103|||2PIQ|||K 103；K103|||K-103|||2PIQ|||K 103
K103 Hydrochloride, an inhibitor of peptidoglycan synthesis, targets the lipid II precursor.
价 格：￥电议型 号：T27705产 地：中国大陆
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T27696JTK-109；化合物JTK-109JTK109；JTK109
JTK-109 is an inhibitor of hepatitis C virus NS5B RNA-dependent RNA polymerase inhibitor and inhibits G1b and G3a subgenomic replicons and recombinant enzymes.
价 格：￥电议型 号：T27696产 地：中国大陆
