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T71040GR-95030X；化合物 GR-95030XGR-95030X
GR-95030X is a a novel HMG-CoA reductase inhibitor.
价 格：￥电议型 号：T71040产 地：中国大陆
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T61040Vin-F03；化合物 Vin-F03Vin-F03
Vin-F03 can be used in the research of type 2 diabetes mellitus that is an effective protective agent of pancreatic β-cells (EC50 = 0.27 μM). Vin-F03 potently promotes the survival of β-cell and protects β-cells from apoptosis induced by STZ[1].
价 格：￥电议型 号：T61040产 地：中国大陆
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T36189CAY10406CAY10406CAY10406|||CAY-10406
CAY10406 is a trifluoromethyl analog of an isatin sulfonamide compound that selectively inhibits caspases 3 and 7. The non-trifluoromethyl compound exhibits Ki values of 1.2 nM and 6 nM for caspases 3 and 7, respectively. For all of the other caspases tested, it is 100 to 1,000 times less potent. Caspases 3 and 7 are ´effector caspases´ that are downstream from the initiating steps of apoptosis, and are implicated in the main proteolytic processing of the apoptotic signal. No data is
价 格：￥电议型 号：T36189产 地：中国大陆
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T31040CP-18 F-18；化合物 T31040CP18 F-18|||CP 18 F-18|||(18F)-CP18；CP18 F-18|||CP 18 F-18|||(18F)-CP18
CP-18 F-18 is a DEVD (the caspase 3 substrate recognition motif) that is an imaging tracer for caspase-3 activity in apoptotic cells.
价 格：￥电议型 号：T31040产 地：中国大陆
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T2S1040Jolkinolide B；岩大戟内酯 BJolkinolide B
Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud. Jolkinolide B induces apoptosis in cancer cells. Jolkinolide B can be used for studies on preventing and treating osteolysis.
价 格：￥电议型 号：T2S1040产 地：中国大陆
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T28852SRI-31040；化合物 T28852SRI 31040；SRI 31040
SRI-31040 is a potent DAT allosteric modulator. It partially inhibits DAT uptake without altering DAT-mediated reverse transport and with minimal inhibition of DAT binding.
价 格：￥电议型 号：T28852产 地：中国大陆
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T25906LOxaprotiline hydrochloride；化合物 T25906LNSC-310406|||NSC310406；NSC-310406|||NSC310406
Oxaprotiline hydrochloride is an antidepressant.
价 格：￥电议型 号：T25906L产 地：中国大陆
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T2443CI-1040化合物CI-1040PD 184352
CI-1040 (PD 184352) (PD184352) is an ATP non-competitive MEK1/2 inhibitor (IC50: 17 nM).
价 格：￥电议型 号：T2443产 地：中国大陆
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T12924Sitaxsentan；司他生坦TBC-11251|||IPI 1040；TBC-11251|||IPI 1040
Sitaxsentan (TBC-11251) is A selective endothelin A (ETA) receptor antagonist. Endothelin is an effective vasoconstrictor. Sitaxsentan blocks the binding of endothelin to its receptors, thereby eliminating the harmful effects of endothelin.
价 格：￥电议型 号：T12924产 地：中国大陆
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T12222Nifedipine-d6；硝苯地平 D6Nifedipine D6|||BAY-a-1040 D6；硝苯地平 D6|||Nifedipine D6|||BAY-a-1040 D6
Nifedipine D6 is deuterium labeled nifedipine which is a potent blocker of calcium channel.
价 格：￥电议型 号：T12222产 地：中国大陆
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T1146Nifedipine；硝苯地平BAY-a-1040|||Procardia XL|||Procardia|||Adalat；BAY-a-1040|||Procardia XL|||Procardia|
Nifedipine (Procardia) is a dihydropyridine calcium channel blocking agent. Nifedipine inhibits the transmembrane influx of extracellular calcium ions into myocardial and vascular smooth muscle cells, causing dilatation of the main coronary and systemic arteries and decreasing myocardial contractility. This agent also inhibits the drug efflux pump P-glycoprotein which is overexpressed in some multi-drug resistant tumors and may improve the efficacy of some antineoplastic agents.
价 格：￥电议型 号：T1146产 地：中国大陆
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T11100DS-1040 Tosylate；化合物 T11100DS-1040 Tosylate
DS-1040 Tosylate is an oral active, selective thrombolytic inhibitor with IC50s of 5.92 nM and 8.01 nM for human and rat TAFIa, is an orally active, selective inhibitor of activated thrombin-activatable fibrinolysis inhibitor (TAFIa) with IC50s of 5.92 nM and 8.01 nM for human and rat TAFIa. DS-1040 Tosylate is a fibrinolysis enhancer for thromboembolic diseases[1].
价 格：￥电议型 号：T11100产 地：中国大陆
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T11040Dihydro Dutasteride；化合物 T11040Dihydro Dutasteride
Dihydro Dutasteride is a metabolite of Dutasteride. Dutasteride is an effective inhibitor of five α-reductase isozymes.
价 格：￥电议型 号：T11040产 地：中国大陆
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T10409ATX inhibitor 5；ATX抑制剂5ATX inhibitor 5
ATX inhibitor 5 is a potent and orally active autotaxin (ATX) inhibitor (IC50 : 15.3 nM) that reduces the level of CCl4-induced hepatic fibrosis and has anti-hepatic fibrosis effects,.
价 格：￥电议型 号：T10409产 地：中国大陆
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T10408ATWLPPR Peptide TFA；化合物 T10408ATWLPPR Peptide TFA
ATWLPPR Peptide TFA is a selective neuropilin-1 inhibitor and inhibits VEGF165 binding to NRP-1. It has the potential in reducing the early retinal damage caused by diabetes.
价 格：￥电议型 号：T10408产 地：中国大陆
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T10407Gartisertib；化合物 T10407ATR inhibitor 2；ATR inhibitor 2
ATR inhibitor 2 is an orally active, ATP-competitive, and selective ATR inhibitor (Ki <150 pM) with antitumor activity. ATR inhibitor 2 potently inhibits ATR-driven phosphorylated checkpoint kinase-1 (Chk1) phosphorylation (IC50: 8 nM).
价 格：￥电议型 号：T10407产 地：中国大陆
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T10406Tuvusertib；化合物TuvusertibM1774|||ATR inhibitor 1；M1774|||ATR inhibitor 1
Tuvusertib (M1774) is an orally available ataxia telangiectasia and Rad3-related (ATR) kinase inhibitor (Ki< 1 ?Μ) with selective and potentially antitumor activity.Tuvusertib selectively inhibits ATR activity and blocks downstream phosphorylation of serine/threonine protein kinase checkpoint kinase 1 (CHK1), thereby inhibits DNA damage checkpoint activation, disrupting DNA damage repair and inducing apoptosis in tumor cells.
价 格：￥电议型 号：T10406产 地：中国大陆
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T10405ATPA；化合物 T10405ATPA
ATPA is a selective glutamate receptor GluR5 activator (EC50s: 0.66, 1.4, 9.5, 23, 32, 18, and 14 μM for GluR5wt, GluR5(S721T), GluR5(S741M), GluR5(S721T, S741M), GluR5(S741A), GluR5(S741L), and GluR5(S741V)).
价 格：￥电议型 号：T10405产 地：中国大陆
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T10404ATP synthase inhibitor 1；化合物ATP synthase inhibitor 1ATP synthase inhibitor 1
ATP synthase inhibitor 1 is an inhibitor of the c subunit of the F1/FO-ATP synthase complex. It inhibits mitochondrial permeability transition pore (mPTP) opening and does not affect ATP levels.
价 格：￥电议型 号：T10404产 地：中国大陆
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T10403Atorvastatin ethyl ester；化合物 T10403Atorvastatin ethyl ester
Atorvastatin ethyl ester, a derivative of Atorvastatin, exhibits potent inhibition of 9-cis-RA-induced Gal4 reporter activity.
价 格：￥电议型 号：T10403产 地：中国大陆
