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产品数：86101
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T6874Lercanidipine hydrochlorideantihypertensive,Inhibitor,calcium,Lercanidipine,Lercanidipine hydrochlor
Lercanidipine is a calcium channel blocker of the dihydropyridine class.
价 格：￥电议型 号：T6874产 地：中国大陆
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T6698Temocapril hydrochloridehypertension,CES1,acute myocardial infarction,Temocapril,Angiotensin-convert
Temocapril HCl, the hydrochloride of Temocapril, is a long-acting ACE inhibitor used for the therapy of hypertension.
价 格：￥电议型 号：T6698产 地：中国大陆
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TN2117Pulsatilloside EChinensioside B,inhibit,Pulsatilloside E,Inhibitor
Pulsatilloside E is a natural product isolated from the roots of Pulsatilla chinensis (Ranunculaceae).
价 格：￥电议型 号：TN2117产 地：中国大陆
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TP2309NEUROTENSIN TFA (39379-15-2 free base)NEUROTENSIN TFA (39379 15 2 free base),NEUROTENSIN TFA (393791
Neurotensin (NT) is an endogenous 13 amino acid neuropeptide with profound opioid-independent analgesic effects. It behaves as a neurotransmitter in the brain, as a hormone in the gut, and also as a neuromodulator. It is implicated in the pathophysiology of several CNS disorders (including schizophrenia, Parkinson´s disease, drug abuse, pain, cancer, inflammation, eating disorders and central control of blood pressure) due to its association with a wide variety of neurotransmitter systems
价 格：￥电议型 号：TP2309产 地：中国大陆
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T7430AM-0902Transient receptor potential channels,TRP Channel,AM 0902,AM-0902,Inhibitor,inhibit,AM0902
AM-0902 is a potent and specific TRPA1 antagonist (IC50s: 71/131 nM for rTRPA1 and hTRPA1).
价 格：￥电议型 号：T7430产 地：中国大陆
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TCS0102PulegoneEndogenous Metabolite,Transient receptor potential channels,TRP Channel,Pulegone,Inhibitor,i
1. Pulegone has cytotoxicity followed by regenerative cell proliferation is the MOA for Pulegone-induced urothelial tumors in female rats. 2. Pulegone induces a verapamil-sensitive psychostimulant effect that appears to independ on the opening of L-type calcium channels. 3. Pulegone has negative reinforcing properties and seems to possess anxiolytic-like actions unrelated to the benzodiazepine site of the γ-aminobutyric acid type A (GABAA) receptor.
价 格：￥电议型 号：TCS0102产 地：中国大陆
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T7575L[Sar1, Ile8]-Angiotensin II 3TFA[Sar1, Ile8] Angiotensin II 3TFA,[Sar1, Ile8]Angiotensin II 3TFA,[Sa
[Sar1, Ile8]-Angiotensin II(3TFA) is a peptide that has multiple effects on vascular smooth muscle.
价 格：￥电议型 号：T7575L产 地：中国大陆
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T8596Ceefourin 1P-glycoprotein,chemosensitizers,inhibit,efflux,protein,resistance,Ceefourin 1,Ceefourin1,
Ceefourin 1 is a highly selective multidrug resistance protein 4 (MRP4) inhibitor.
价 格：￥电议型 号：T8596产 地：中国大陆
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TN1911MareinGLUT1,HDAC,Inhibitor,Akt,inhibit,antioxidative,Marein,Histone deacetylases,antihypertensive,AM
Marein shows neuroprotective effect on PC12 cell damage induced by methylglyoxal, which is due to a reduction of damage to mitochondria function and activation of the AMPK signal pathway, it may be a potent compound for preventing/counteracting diabetic encephalopathy.
价 格：￥电议型 号：TN1911产 地：中国大陆
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T6667SF1670inhibit,Autophagy,SF1670,MMAC1,Inhibitor,SF 1670,SF-1670,Phosphatase and tensin homolog,Phosph
SF1670 is a specific PTEN inhibitor with IC50 of 2 μM.
价 格：￥电议型 号：T6667产 地：中国大陆
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T8900SeralutinibPK 10571,Seralutinib,inhibit,arterial,PDGFR,PK10571,PK-10571,PAH,Pulmonary,hypertension,G
Seralutinib is an inhibitor of inhaled PDGFRα and PDGFRβ. It is used in the study for pulmonary arterial hypertension.
价 格：￥电议型 号：T8900产 地：中国大陆
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T6848GSK1016790Ainhibit,Ca2+ channels,Inhibitor,embryonic,GSK-1016790A,Ca channels,HEK,vanilloid,transien
GSK1016790A (GSK101) is a novel, potent activator of TRPV4 (transient receptor potential vanilloid 4) with EC50 of 34 nM in choroid plexus epithelial cells.
价 格：￥电议型 号：T6848产 地：中国大陆
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T8403CinacalcetAMG-073,Calcium-sensing receptor,Endogenous Metabolite,Inhibitor,CaSR,Cinacalcet,inhibit,A
Cinacalcet is an orally active, allosteric Ca receptor (CaR) agonist, treatment of cardiovascular disease .
价 格：￥电议型 号：T8403产 地：中国大陆
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T6S1369Vitexinneurodegeneration,Vitexin,anti-cancer,anti-nociceptive,inhibit,Medicinal,anti-hypertensive,an
1. Vitexin has antinociceptive and antispasmodic activities. 2. Vitexin exhibits a prominent first-pass effect. 3. Vitexin has antioxidant, antimyeloperoxidase, and α-glucosidase inhibitory activities. 4. Vitexin can either inhibit or induce activities of CYP2C11 and CYP3A1. 5. Vitexin induces the novel p53-dependent metastatic and apoptotic pathway. 6. Vitexin protects brain against cerebral I/R injury, and this effect may be regulated by mitogen-activated protein kinase (MAPK) and apoptosis si
价 格：￥电议型 号：T6S1369产 地：中国大陆
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T6951Pramipexole dihydrochloride hydratetransient,Pramipexole dihydrochloride,Pramipexole dihydrochloride
Pramipexole Dihydrochloride is the hydrochloride salt of pramipexole, a benzothiazole derivative. As a nonergot dopamine agonist, pramipexole binds to D2 and D3 dopamine receptors in the striatum and substantia nigra of the brain.
价 格：￥电议型 号：T6951产 地：中国大陆
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T7714TemocapilMn-SOD,inhibit,Temocaprilat,Cu/ZnSOD,renal diseases,heart failure,hypertension,Temocapril,i
Temocapril is an inhibitor of tyrosine kinase.
价 格：￥电议型 号：T7714产 地：中国大陆
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T9716Ensitrelvirintrapulmonary replication,Virus Protease,COVID-19,S217622,oral,SARS-CoV,Ensitrelvir,SARS
Ensitrelvir is an orally active inhibitor of SARS-CoV-2 3CL protease with IC50 of 13 nM.
价 格：￥电议型 号：T9716产 地：中国大陆
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T8580Bupranololnon-selective,competitive,Adrenergic Receptor,Bupranolol,Inhibitor,intrinsic,sympathomimet
Bupranolol is an antagonist of β2-adrenergic receptor and has been used for angina pectoris, hypertension, glaucoma, cardiac arrhythmia and as an antithrombotic.
价 格：￥电议型 号：T8580产 地：中国大陆
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TN1117VeraguensinVeraguensin
Veraguensin is derived from Magnolia sp.. Veraguensin inhibits bone resorption and shows high antileishmanial activity.
价 格：￥电议型 号：TN1117产 地：中国大陆
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T8457NPS2390Inhibitor,NPS2390,Calcium-sensing receptor,NPS-2390,mGluR,inhibit,Metabotropic glutamate rece
NPS2390 is a first generation quinoxaline derivative that acts as a noncompetitive antagonist of mGluR1 and mGluR5 (IC50 of 5.2 and 82 nM, respectively)
价 格：￥电议型 号：T8457产 地：中国大陆
