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产品数：86101
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TN2007OJV-VIOJVVI,inhibit,OJV VI,OJV-VI,Inhibitor
OJV-VI is a natural product found in ophiopogonis.
价 格：￥电议型 号：TN2007产 地：中国大陆
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T3S2007MRE-269ACT-333679；MRE 269；MRE269；3-氧代-12-烯-28-乌苏酸
MRE-269 is an orally available and long-acting prostacyclin receptor agonist prodrug. MRE-269 is used for the treatment of pulmonary arterial hypertension. MRE-269 is an active metabolite of Selexipag (S253150).
价 格：￥电议型 号：T3S2007产 地：中国大陆
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T2007RQ-00203078RQ00203078
RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist.
价 格：￥电议型 号：T2007产 地：中国大陆
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T2007RQ00203078RQ00203078
RQ-00203078 is a highly selective, potent and orally available TRPM8 antagonist.
价 格：￥电议型 号：T2007产 地：美洲
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T82964ARUK2007145；化合物 ARUK2007145ARUK2007145
ARUK2007145 is a potent, cell-active inhibitor targeting both PI5P4Kα and PI5P4Kγ isoforms with pIC50 values of 7.3 and 8.1, respectively [1].
价 格：￥电议型 号：T82964产 地：中国大陆
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T82007JH-131e-153；化合物 JH-131e-153JH-131e-153
JH-131e-153, a diacylglycerol (DAG)-lactone, serves as a small molecule activator for the C1 domain of Munc13-1, exhibiting an activation hierarchy of WT>I590≈R592A≈W588A. This compound’s C1 domain shares homology in sequence and structure with protein kinase C (PKC), and its activation preference follows the order of PKCα>Munc13-1>PKCε. JH-131e-153 is implicated in the modulation of neuronal processes and holds potential for research in neurodegenerative diseases [1].
价 格：￥电议型 号：T82007产 地：中国大陆
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T74905ODN 2007；化合物 ODN 2007ODN 2007
ODN 2007, a class B CpG ODN (oligodeoxynucleotide) and Toll-like receptor (TLR) ligand, serves as an immunomodulator and vaccine adjuvant, promoting enhanced immune responses across mammals, fish, and humans. Its sequence is 5´-TCGTCGTTGTCGTTTTGTCGTT-3´ [1] [2] [3].
价 格：￥电议型 号：T74905产 地：中国大陆
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T72007COR167；化合物 COR167COR167
COR167 is a CB2 agonist. It displayed potent immunomodulatory activity on immune cells from healthy subjects and patients with multiple sclerosis. It also showed protective effects on rat brain tissues toward ischemia and reperfusion-induced injury. COR167 has antinociceptive properties.
价 格：￥电议型 号：T72007产 地：中国大陆
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T71772Bicifadine free base；化合物 Bicifadine free baseCL-220075|||Bicifadine free base|||CL220075|||Bicifadin
Bicifadine, also known as DOV-220075, CL 220,075, is a SNDR inhibitor potentially for the treatment of lower back pain. Bicifadine has a non-opioid, non-NSAID mechanism for the treatment of pain, which should have less abuse potential than opioid drugs and less propensity to cause gastric ulcers than NSAID drugs. While the drug is purported to be a serotonin (SERT) and noradrenaline transporter (NET) inhibitor, it also has effects at the dopamine transporter (DAT), effectively making it a broad
价 格：￥电议型 号：T71772产 地：中国大陆
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T69831RPR-200765A Mesylayte；化合物 RPR-200765A MesylayteRPR-200765A Mesylayte
RPR-200765A is a potent and selective inhibitor of p38 MAP kinase (IC50 = 50 nM). It inhibits LPS-stimulated TNFalpha release both in vitro, from human monocytes (EC50 = 110 nM), and in vivo in Balb/c mice (ED50 = 6 mg/kg). At oral doses between 10 and 30 mg/kg/day it reduces the incidence and progression in the rat streptococcal cell wall (SCW) arthritis model when administered in either prophylactic or therapeutic dosing regimens. The compound, which is a mesylate salt and exists as a stable m
价 格：￥电议型 号：T69831产 地：中国大陆
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T62007CXCR4 modulator-1；化合物 CXCR4 modulator-1CXCR4 modulator-1
CXCR4 modulator-1 (compound ZINC72372983) is a potent CXCR4 modulator (EC 50= 100 nM). CXCR4 modulator-1 has research value in anti-inflammatory, anticancer and anti-HIV.
价 格：￥电议型 号：T62007产 地：中国大陆
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T3S2007MRE-269；3-氧代-12-烯-28-乌苏酸3-氧代-12-烯-28-乌苏酸|||ACT-333679|||ACT-333679|||MRE-269|||MRE-269|||MRE 269|||M
MRE-269 (ACT-333679) is an orally available and long-acting prostacyclin receptor agonist prodrug. MRE-269(ACT-333679) is used for the treatment of pulmonary arterial hypertension. MRE-269(ACT-333679) is an active metabolite of Selexipag (S253150).
价 格：￥电议型 号：T3S2007产 地：中国大陆
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T33479Monoxerutin；单羟乙基芦丁Z 12007|||MonoHER|||7-Monohydroxyethylrutosid；Z 12007|||MonoHER|||7-Monohydroxyeth
Monoxerutin (MonoHER) is a vasodilator with antioxidant activity that prevents adriamycin-induced cardiotoxicity in mice and is used in the study of acute respiratory syndrome.
价 格：￥电议型 号：T33479产 地：中国大陆
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T32007GSK256471；化合物 T32007GSK 256471|||GSK-256471；GSK 256471|||GSK-256471
GSK256471 is a potent selective NK(3) antagonist that shows a high affinity for recombinant human (PK (I) value 8.9) and native guinea pig (PK (I) value 8.4) tachykinin NK(3) receptors. In vitro functional assessment showed that GSK256471 reduced the E(Max) response induced by neurokinin B, indicating insurgable antagonist pharmacology (PA (2)=9.2). GSK256471 may be a promising candidate for the treatment of schizophrenia.
价 格：￥电议型 号：T32007产 地：中国大陆
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T28534RH02007；化合物 T28534CCG 40788|||RH-02007|||CCG40788|||CCG-40788|||RH 02007；CCG 40788|||RH-02007|||CCG4
RH02007 is an inhibitor of the human papillomavirus (HPV) E6 oncoprotein.
价 格：￥电议型 号：T28534产 地：中国大陆
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T24346L 702007；化合物 T243465-Emmpo|||L702007|||L-702007；5-Emmpo|||L702007|||L-702007
L 702007 is an inhibitor of HIV-1 reverse transcriptase.
价 格：￥电议型 号：T24346产 地：中国大陆
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T20078Tributyl phosphite；化合物 T20078BRN 1703866|||NSC2675|||NSC 2675|||Tributoxyphosphine|||NSC-2675|||Trib
Tributyl phosphite is an alkyl phosphite. It is reported to inhibit carboxylesterase activity.
价 格：￥电议型 号：T20078产 地：中国大陆
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T20076Irganox 1010；化合物Irganox 1010Dovernox 10；Dovernox 10
Irganox 1010 (Dovernox 10) is an agent of antioxidant.
价 格：￥电议型 号：T20076产 地：中国大陆
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T20075Sodium dodecyl sulfate；月桂基硫酸钠盐Laurylsulfuric acid sodium salt|||NSC 402488|||Anticerumen|||NSC-40248
Sodium dodecyl sulfate(Sodium lauryl sulfate) is a pharmaceutical excipient that is biologically inactive and improves the stability, solubility and processability of pharmaceutical preparations.
价 格：￥电议型 号：T20075产 地：中国大陆
