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产品数：86101
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T7817Aprocitentaninhibit,Endothelin Receptor,ACT132577,Aprocitentan,Inhibitor,ACT 132577
Aprocitentan is ETA and ETB antagonist .
价 格：￥电议型 号：T7817产 地：中国大陆
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TN7163Methyl 4-bromopyrrole-2-carboxylate
Methyl 4-bromopyrrole-2-carboxylate is a marine derived natural products found in Lissodendoryx sp.
价 格：￥电议型 号：TN7163产 地：中国大陆
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TQ01548-HydroxyguanosineEndogenous Metabolite,8 Hydroxyguanosine,Inhibitor,8Hydroxyguanosine,8-Hydroxyguan
8-hydroxyguanosine (8-OHG) is a marker for measuring the rate of oxidative damage to nucleic acids and lipids.
价 格：￥电议型 号：TQ0154产 地：中国大陆
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T6953Prilocainelocal,anaesthetize,inhibit,Inhibitor,Sodium potassium pump,Na(+),K(+),neurotoxic,Na+/K+ AT
Prilocaine is a local anesthetic of the amino amide type, which acts on the sodium channel on the neuronal membrane and limits the spread of seizures.
价 格：￥电议型 号：T6953产 地：中国大陆
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TQ0046BavisantJNJ31001074,JNJ 31001074,Neurological disorders,inhibit,Histamine Receptor,attention-deficit
Bavisant is a selective and orally active Human H3 receptor antagonist. Bavisant can be used in research on mechanisms of action, involving wakefulness and cognition and the treatment for ADHD.
价 格：￥电议型 号：TQ0046产 地：中国大陆
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T7221SatraplatinBMY 45594,DNA Alkylator/Crosslinker,BMS-182751,Satraplatin,BMY-45594,JM 216,inhibit,Inhib
Satraplatin is an orally available antineoplastic platinum(IV) complex.Satraplatin has a favorable toxicity profile and appears to have clinical activity against a variety of malignancies.
价 格：￥电议型 号：T7221产 地：中国大陆
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T9521CHR-6494 TFACHR-6494,inhibit,apoptosis,Haspin Kinase,NRAS mutant melanoma cells,CHR 6494,mitotic cat
CHR-6494 TFA is a potent haspin inhibitor, with an?IC50?of 2 nM. It inhibits histone H3T3 phosphorylation. CHR-6494 TFA induces the?apoptosis?of cancer cells, including melanoma and breast cancer. CHR-6494 TFA can be used in the research of cancer
价 格：￥电议型 号：T9521产 地：中国大陆
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T6S0052ChelerythrineBcl-2 Family,Apoptosis,Protein kinase C,PKC,Inhibitor,Chelerythrine,inhibit,Autophagy
1. Chelerythrine may have antimanic effect . 2. Chelerythrine can inhibit telomerase activity. 3. Chelerythrine is a well-known protein kinase C inhibitor . 4. Chelerythrine has potential antiproliferative and antitumor effects.
价 格：￥电议型 号：T6S0052产 地：中国大陆
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T9172Simufilam dihydrochlorideInhibitor,PTI-125,Simufilam,inhibit,PTI 125,PTI125,Simufilam dihydrochlorid
Simufilam dihydrochloride is a low toxicity, orally active filamin A (FLNA) activator, which can be used for the research of Alzheimer´s disease. Simufilam dihydrochloride preferentially binds altered FLNA and restores its native conformation, restoring receptor and synaptic activities and reducing its α7nAChR/TLR4 associations and downstream pathologies.
价 格：￥电议型 号：T9172产 地：中国大陆
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T7370TalarozoleRetinoid X receptors,R 115866,Retinoic acid receptors,RAR/RXR,inhibit,Talarozole,Cytochrom
Talarozole is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.Talarozole for the treatment of acne, psoriasis and other keratinization disorders.
价 格：￥电议型 号：T7370产 地：中国大陆
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T8476RSVA405RSVA-405,Autophagy,Inhibitor,anti-inflammatory,STAT,AMP-activated protein kinase,disease,Kina
RSVA 405 is an AMPK activator (EC50 = 1 μM), and is STAT3 inhibitor
价 格：￥电议型 号：T8476产 地：中国大陆
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T8822JNJ-5207852 dihydrochlorideInhibitor,toxicity,JNJ5207852,inhibit,low,JNJ 5207852,sleep,REM,JNJ-52078
JNJ-5207852 is a novel, non-imidazole histamine H3 receptor antagonist, with high affinity at the rat (pKi=8.9) and human (pKi=9.24) H3 receptor.
价 格：￥电议型 号：T8822产 地：中国大陆
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T8158Tilianinantioxidant,Inhibitor,inflammatory,myocardial-protective,diabetic,hyperlipidemic,inhibit,Til
Tilianin is a flavonoid glycoside of Dragocephalum moldavicum L.
价 格：￥电议型 号：T8158产 地：中国大陆
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T74501-Phenylpropane-1,2-dione1Phenylpropane1,2dione,ephedrine,Ephedra,alkaloids,Inhibitor,precursors,sin
1-Phenyl-1,2-propanedione is a eukaryotic metabolite produced in plant metabolic reactions.
价 格：￥电议型 号：T7450产 地：中国大陆
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T828814-Deoxyandrographolideplatelet activating factor,rat,bovine neutrophils,14 Deoxyandrographolide,Cal
14-Deoxyandrographolide is a bioactive compound of Andrographis paniculata with hepatoprotective efficacy. It desensitizes hepatocytes to TNF-α-mediated apoptosis through the release of TNFRSF1A release.
价 格：￥电议型 号：T8288产 地：中国大陆
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TP1065PAR-4 Agonist Peptide, amide TFAThrombin receptors,PAR4 Agonist Peptide, amide TFA,Protease Activate
PAR-4 Agonist Peptide, amide TFA is a proteinase-activated receptor-4 (PAR-4) agonist, which has no effect on either PAR-1 or PAR-2 and whose effects are blocked by a PAR-4 antagonist.
价 格：￥电议型 号：TP1065产 地：中国大陆
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T6S2315Polyphyllin VIPolyphyllin VI,inhibit,Pyroptosis,Apoptosis,Inhibitor
1. Polyphyllin VI has hemostasis , expectorant , bacteriostasis, anticytotoxic, anti pregnancy kill sperm effects.
价 格：￥电议型 号：T6S2315产 地：中国大陆
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TN3575(±)-CannabichromeneInhibitor,(±)-Cannabichromene,(±)Cannabichromene,(±) Cannabichromene,DL-cannabich
Cannabichromene is a major non-psychotropic phytocannabinoid that inhibits endocannabinoid inactivation and activates the transient receptor potential ankyrin-1 (TRPA1), it selectively reduces inflammation-induced hypermotility in vivo in a manner that is not dependent on cannabinoid receptors or TRPA1.
价 格：￥电议型 号：TN3575产 地：中国大陆
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T7522GI254023XSRI 028594,SRI028594,GI 4023,inhibit,GI-254023X,Matrix metalloproteinases,SRI-028594,Inhibi
GI254023X is a potent MMP9 and ADAM10 inhibitor (IC50s: 2.5 and 5.3 nM) with 100-fold selectivity for the α-secretase ADAM10 over ADAM17 (TACE). GI254023X can remarkably inhibit the proliferation and induce the apoptosis of H929 cells. Its mechanism may be associated with inbihition of Notch1 activation.
价 格：￥电议型 号：T7522产 地：中国大陆
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T9734Benzo[b]thiophene-2-sulfonamide, N-[3-(aminomethyl)phenyl]-5-chloro-3-methyl-Benzo[b]thiophene2sulfo
Benzo[b]thiophene-2-sulfonamide, N-[3-(aminomethyl)phenyl]-5-chloro-3-methyl- directly inhibits InhA and does not require activation by the catalase peroxidase KatG.
价 格：￥电议型 号：T9734产 地：中国大陆
