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T70399TTC-352；化合物 TTC-352TTC-352
TTC-352 is an orally bioavailable selective human estrogen receptor alpha (ERalpha; ESR1; ERa) partial agonist (ShERPA), with potential antineoplastic activity. Upon administration, TTC-352 mimics the naturally-occurring 17beta-estradiol (E2) and targets and binds to ERa located in the nucleus. This causes translocation of ERa to extranuclear sites. Nuclear export of ERa prevents normal ER-mediated signaling and inhibits proliferation of ER-positive tumor cells.
价 格：￥电议型 号：T70399产 地：中国大陆
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T70151MeTC7；化合物 MeTC7MeTC7
MeTC7 is a VDR antagonist, which can be synthesized from 7-dehydrocholesterol (6) in two steps, inhibits VDR selectively, suppresses the viability of cancer cell-lines, and reduces the growth of the spontaneous transgenic TH-MYCN neuroblastoma and xenografts in vivo.
价 格：￥电议型 号：T70151产 地：中国大陆
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T70022TC299423；化合物 TC299423TC299423
TC299423 is a novel agonist for nicotinic acetylcholine receptors (nAChRs). TC299423 modestly selectively targets α6β2 subtype.
价 格：￥电议型 号：T70022产 地：中国大陆
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T69633TCS-401；化合物 TCS-401TCS-401
TCS-401 is an insulin receptor sensitizing agent; Selective inhibitor of protein-tyrosine phosphatase 1B (PTP1B).
价 格：￥电议型 号：T69633产 地：中国大陆
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T69624TC-5115；化合物 TC-5115TC-5115
TC-5115 is a potent inhibitor of MLL methyltransferase with IC50 value of 16 nM. TC-5115 may lead to the development of a new therapy for the treatment of human MLL leukemia. The mixed-lineage leukemia (MLL) protein, also known as MLL1, is a lysine methyltransferase specifically responsible for methylation of histone 3 lysine 4. MLL has been pursued as an attractive therapeutic target for the treatment of acute leukemia carrying the MLL fusion gene or MLL leukemia.
价 格：￥电议型 号：T69624产 地：中国大陆
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T69623Tridemorph；化合物 TridemorphTC5115|||Tridemorph|||TC 5115；TC5115|||Tridemorph|||TC 5115
Tridemorph is a sterol biosynthetic inhibitor. It is a fungicide used to control Erysiphe graminis. It was developed by BASF in the 1960s who use the trade name Calixin. The World Health Organization has categorized it as a Class II moderately hazardous" pesticide because it is believed harmful if swallowed and can cause irritation to skin and eyes."
价 格：￥电议型 号：T69623产 地：中国大陆
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T69356Cindunistat；化合物CindunistatCindunistat free base|||SD6010|||SD-6010；Cindunistat free base|||SD6010|||
Cindunistat (free base) is an orally available selective iNOS inhibitor for the study of arthritis.
价 格：￥电议型 号：T69356产 地：中国大陆
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T69170ATC0065 HCl；化合物 ATC0065 HClATC0065 HCl
ATC0065 dihydrochloride is a novel nonpeptidic and potent melanin-concentrating hormone receptor 1 (MCHR1) selective antagonist.
价 格：￥电议型 号：T69170产 地：中国大陆
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T69073COTC；化合物 COTCCOTC
COTC is a bacterial metabolite that has anticancer activity and inhibits glyoxalase in the presence of glutathione (GSH) and the proliferation of HeLa cells, as well as reduces tumor growth and improves survival in an Ehrlich murine spontaneous adenocarcinoma model.
价 格：￥电议型 号：T69073产 地：中国大陆
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T68697TC-1698 dihydrochloride；化合物 TC-1698 dihydrochlorideTC-1698 dihydrochloride
TC-1698 dihydrochloride is a selective nicotinic α7 receptor agonist that also displays weak partial agonist/antagonist activity at β-subunit-containing receptors. This product is a neuroprotectant.
价 格：￥电议型 号：T68697产 地：中国大陆
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T68433Clinprost；化合物 ClinprostClinprost
Clinprost is a Vasodilator (peripheral), Platelet aggregation inhibitor, and Prostaglandin I2 receptor agonist
价 格：￥电议型 号：T68433产 地：中国大陆
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T68412Cilazaprilat；化合物 CilazaprilatCilazaprilat
Cilazaprilat is the active metabolite of cilazapril, a pyridazine angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity.
价 格：￥电议型 号：T68412产 地：中国大陆
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T68351Homodestcardin；化合物 HomodestcardinHomodestcardin
Homodestcardin is a cyclic depsipeptide fungal metabolite that has been found in T. roseum and has immunosuppressant activity. It inhibits concanavalin A-induced proliferation of isolated mouse T cells.
价 格：￥电议型 号：T68351产 地：中国大陆
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T68154TC-2216；化合物TC-2216TC-2216
TC-2216 is a partial agonist at the neural nicotinic acetylcholine receptor and is used to treat anxiety and depression.
价 格：￥电议型 号：T68154产 地：中国大陆
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T6767TCS7010；化合物Aurora A Inhibitor IAurora A Inhibitor I；Aurora A Inhibitor I
TCS7010 (Aurora A Inhibitor I) is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B.
价 格：￥电议型 号：T6767产 地：中国大陆
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T6697TCID；化合物TCIDUCH-L3 Inhibitor；UCH-L3 Inhibitor
TCID (UCH-L3 Inhibitor)(IC50=0.6 μM) is a DUB inhibitor of ubiquitin C-terminal hydrolase L3. It has the 125-fold selectivity to L1.
价 格：￥电议型 号：T6697产 地：中国大陆
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T6553LJTC-801 free base；化合物 T6553LJTC-801；JTC-801
JTC-801 is a selective antagonist of the opioid receptor-like1 receptor (Ki: 8.2 nM).
价 格：￥电议型 号：T6553L产 地：中国大陆
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T6553JTC-801；化合物JTC801JTC 801|||JTC801；JTC 801|||N-(4-氨基-2-甲基-6-喹啉基)-2-[(4-乙基苯氧基)甲基]苯甲酰胺盐酸盐|||JTC801
JTC-801 is a selective opioid receptor-like1 (ORL1) receptor antagonist with IC50 of 94 nM, weakly inhibits receptors δ, κ, and μ.
价 格：￥电议型 号：T6553产 地：中国大陆
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T65061CAPS sodium salt；化合物 CAPS sodium saltCAPS sodium salt
CAPS sodium salt is a useful organic compound for research related to life sciences. The catalog number is T65061 and the CAS number is 105140-23-6.
价 格：￥电议型 号：T65061产 地：中国大陆
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T64759Chondroitin sulfate A sodium salt；化合物 Chondroitin sulfate A sodium saltChondroitin sulfate A sodium
Chondroitin sulfate A sodium salt is a useful organic compound for research related to life sciences and the catalog number is T64759.
价 格：￥电议型 号：T64759产 地：中国大陆
