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T1783LXR-623；化合物LXR623LXR623|||WAY 252623；LXR623|||WAY 252623
LXR-623 (WAY 252623) is an orally bioavailable and highly specifical synthetic modulator of LXR.
价 格：￥电议型 号：T1783产 地：中国大陆
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T17256Wnt pathway activator 1；化合物Wnt pathway activator 1Wnt pathway activator 1
Wnt pathway activator 1 is a potent Wnt activator with an IC50 of 28-29 nM. Wnt pathway activator 1 is a potent Wnt activator for the treatment of androgenetic alopecia (AGA).
价 格：￥电议型 号：T17256产 地：中国大陆
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T17253WAY 163909；化合物 T17253WAY 163909
WAY 163909 is an effective and selective agonist of the 5-HT(2C) receptor (Ki: 10.5±1.1 nM).
价 格：￥电议型 号：T17253产 地：中国大陆
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T17251VNA-932；化合物 VNA-932WAY-VNA 932；WAY-VNA 932
VNA-932 is an agonist of the vasopressin V2-receptor (IC50: 80.3 nM and 778 nM in human-V2 binding and V1a binding assay).
价 格：￥电议型 号：T17251产 地：中国大陆
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T17239VU0155069；化合物VU0155069CAY10593；CAY10593
VU0155069 strongly inhibits the invasive migration of several cancer cell lines in transwell assays. VU0155069 is a selective phospholipase D1 inhibitor (IC50: 46 nM in vitro).
价 格：￥电议型 号：T17239产 地：中国大陆
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T17226Vericiguat；维利西呱BAY1021189；维利西呱|||BAY1021189
Vericiguat (BAY1021189) is a potent and orally available guanylate cyclase stimulator.
价 格：￥电议型 号：T17226产 地：中国大陆
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T17114Tolrestat；托瑞司他AY-27773；托瑞司他|||AY-27773
Tolrestat (AY-27773) is a potent inhibitor of aldose reductase (IC50 = 35 nM).
价 格：￥电议型 号：T17114产 地：中国大陆
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T16986Tanomastat；化合物 T16986BAY 12-9566；BAY 12-9566
Tanomastat is an orally bioavailable and non-peptidic biphenyl matrix metalloproteinases inhibitor. For MMP-2, MMP-3, MMP-9, MMP-13 the Ki values are 11, 143, 301, and 1470 nM respectively.
价 格：￥电议型 号：T16986产 地：中国大陆
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T16909Donafenib；多纳非尼Sorafenib (D3)|||Bay 43-9006 (D3)|||Sorafenib-d3；Sorafenib (D3)|||Bay 43-9006 (D3)|||S
Donafenib (Bay 43-9006 (D3)) is a deuterium-labeled Sorafenib which is a multikinase inhibitor(IC50s: 6 nM, 20 nM, and 22 nM for Raf-1, B-Raf, and VEGFR-3, respectively).
价 格：￥电议型 号：T16909产 地：中国大陆
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T16784Roniciclib；化合物RoniciclibBAY 1000394；BAY 1000394
Roniciclib (BAY 1000394) is a potent pan-CDK inhibitor and a novel oral cytotoxic agent. Roniciclib inhibits the activity of cell-cycle CDKs CDK1, CDK2, CDK3, CDK4, and of transcriptional CDKs CDK7 and CDK9 with IC(50) values in the range between 5 and 25 nmol/L.
价 格：￥电议型 号：T16784产 地：中国大陆
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T16781Rogaratinib；化合物RogaratinibBAY1163877；BAY1163877
Rogaratinib (BAY1163877) is an aberrant inhibitor of fibroblast growth factor receptor (FGFR). Rogaratinib is as an orally available, selective and potent inhibitor of FGFR-1, -2 and -3 kinase activity.
价 格：￥电议型 号：T16781产 地：中国大陆
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T16576Pritelivir mesylate化合物 T16576BAY 57-1293 mesylate|||AIC316 mesylate
Pritelivir mesylate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate shows antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.
价 格：￥电议型 号：T16576产 地：中国大陆
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T16575Pritelivir mesylate hydrate化合物 T16575BAY 57-1293 mesylate hydrate|||AIC316 mesylate hydrate
Pritelivir mesylate hydrate is active against herpes simplex virus types 1 and 2 (IC50: 0.02 μM against HSV1-2). Pritelivir mesylate hydrate is an inhibitor of the viral helicase-primase complex. Pritelivir mesylate hydrate shows antiviral activity in vitro and in animal models of herpes simplex virus (HSV) infection.
价 格：￥电议型 号：T16575产 地：中国大陆
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T1640Ciprofloxacin环丙沙星Ciproxan|||环丙沙星|||Ciprobay|||Bay o 9867|||Bay-09867
Ciprofloxacin (Bay-09867), a synthetic broad spectrum fluoroquinolone antibiotic, inhibits bacterial DNA gyrase. It is more active against Gram-negative bacteria than Gram-positive bacteria.
价 格：￥电议型 号：T1640产 地：中国大陆
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T1617Enrofloxacin；恩诺沙星BAY-Vp2674|||PD160788；恩诺沙星|||BAY-Vp2674|||PD160788
Enrofloxacin (BAY-Vp2674) is a veterinary antibacterial agent, used in poultry.
价 格：￥电议型 号：T1617产 地：中国大陆
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T16016Maytansinol；美登醇Ansamitocin P-0；美登醇|||Ansamitocin P-0
Maytansinol (Ansamitocin P-0) inhibits microtubule assembly and causes microtubule disassembly in vitro.
价 格：￥电议型 号：T16016产 地：中国大陆
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T15766Lirimilast；化合物 T15766BAY 19-8004；BAY 19-8004
Lirimilast is an effective, selective, and orally active phosphodiesterase-4 (PDE4) inhibitor (IC50: 49 nM). Lirimilast has potently anti-inflammatory properties. Lirimilast can be used for the treatment of asthma or chronic obstructive pulmonary disease.
价 格：￥电议型 号：T15766产 地：中国大陆
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T15412GPP78；化合物 T15412CAY10618；CAY10618
GPP78 is a potent inhibitor of Nampt (IC50: 3.0 nM for nicotinamide adenine dinucleotide (NAD) depletion). GPP78 is cytotoxic to neuroblastoma cell line SH-SY5Y cells (IC50: 3.8 nM by inducing autophagy). GPP78 has anti-cancer and anti-inflammatory effects.
价 格：￥电议型 号：T15412产 地：中国大陆
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T15370GANT 58；化合物GANT 58NSC 75503；4,44乔,4乔(2,3,4,5-Thiophentetrayl)tetrakis-pyridine|||NSC 75503
GANT 58 (NSC-75503) is a potent antagonist of Gli. Which inhibits GLI1-induced transcription (IC50: 5 μM).
价 格：￥电议型 号：T15370产 地：中国大陆
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T1537Rapamycin；雷帕霉素Sirolimus|||AY 22989|||NSC-2260804；Sirolimus|||AY 22989|||雷帕霉素|||NSC-2260804
Rapamycin (AY 22989) is a natural product of macrolides, an mTOR inhibitor with specificity (HEK293 cells: IC50=0.1 nM). Rapamycin has immunosuppressive activity and induces autophagy.
价 格：￥电议型 号：T1537产 地：中国大陆
