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T16751Rilapladib
Rilapladib is a selective inhibitor of Lipoprotein-Associated Phospholipase A2(Lp-PLA2, IC50 = 230 pM) and an antagonist of the platelet activating factor receptor.
价 格:¥电议型 号:T16751产 地:中国大陆
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T11665Ionomycin calciumCa2+ channels,PKC,ionophore,Calcium Channel,Ionomycin,SQ 23377,Ionomycin calcium,An
lonomycin calcium is a potent, selective calcium ionophore and an antibiotic produced by Streptomyces conglobatus. also induces the activation of protein kinase C (PKC). Ionomycin calcium is highly specific for divalent cations (Ca>Mg>Sr=Ba). Ionomycin promotes apoptosis.
价 格:¥电议型 号:T11665产 地:中国大陆
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TQ0122LVCH-916 free acid(1200133-34-1 free base)VCH 916 free acid(1200133 34 1 free base),VCH916 free acid(
VCH-916 is a novel nonnucleoside HCV NS5B polymerase inhibitor.
价 格:¥电议型 号:TQ0122L产 地:中国大陆
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T6S1688(1E,6E)-Bis(demethoxy)curcumin(E,E)-Curcumin III,Bisdemethoxycurcumin,inhibit,(E,E)-Didemethoxycurcu
(1E,6E)-Bis(demethoxy)curcumin is a natural demethoxy derivative of curcumin,with anti-inflammatory and anti-cancer activities.
价 格:¥电议型 号:T6S1688产 地:中国大陆
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T9018JHU37160Inhibitor,hM4Di,Clozapine,hM3Dq,DREADD,inhibit,Muscarinic acetylcholine receptor,JHU-37160,J
JHU 37160 is a Designer Receptors Exclusively Activated by Designer Drug (DREADD) agonist with Ki of 1.9 nM and 3.6 nM for human muscarinic acetylcholine M3 receptors (hM3Dq) and hM4Di in vitro, respectively. And EC50 values are 18.5 nM and 0.2 nM for hM3Dq and hM4Di in fluorescent and BRET-based assays in HEK-293 cells, respectively.
价 格:¥电议型 号:T9018产 地:中国大陆
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T16401Org-12962Org 12962,Org12962
Org-12962 is an effective and selective 5-HT2C?receptor agonist pEC50: 7.01). Org-12962 shows antiaversive effects in a rat model of panic-like anxiety. Org-12962 also shows high effacy for the 5-HT2A?and 5-HT2B receptors (pEC50s: 6.38 and 6.28, respectively).
价 格:¥电议型 号:T16401产 地:中国大陆
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T7811Pilsicainide HClatrial tachyarrhythmias,SUN-1165,Pilsicainide HCl,antiarrhythmic,inhibit,orally acti
Pilsicainide HCl is a pure sodium channel blocker
价 格:¥电议型 号:T7811产 地:中国大陆
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T9165AZD5305repair,AZD5305,Inhibitor,poly ADP ribose polymerase,DNA,AZD-5305,PARP,inhibit,pathway,synthet
AZD5305 is a potent, selective and oral active PARP inhibitor.
价 格:¥电议型 号:T9165产 地:中国大陆
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TN71694-Hydroxy-3-Nitrobenzyl Alcohol
4-Hydroxy-3-Nitrobenzyl Alcohol is a marine derived natural products found in Phidolopora pacifica.
价 格:¥电议型 号:TN7169产 地:中国大陆
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T8916WEE1-IN-3WEE1IN3,cycle,Inhibitor,inhibit,cell,Wee1,WEE-1-IN-3,WEE1 IN 3,Anticancer
JUN76288 is a potent Wee1 kinase inhibitor with an IC50 of <10 nM. It treatment of cancer and other proliferative diseases.
价 格:¥电议型 号:T8916产 地:中国大陆
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TN7028Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12
Picras-3-en-16-one, 11,20-epoxy-2-(β-D-glucopyranosyloxy)-1,11,12,14,15-pentahydroxy-, (1β,2α,11β,12α,15β)- is a chemical compound.
价 格:¥电议型 号:TN7028产 地:中国大陆
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T6441CGS 21680 HydrochlorideCGS-21680,Inhibitor,CGS 21680,inhibit,CGS21680,CGS 21680 Hydrochloride,Adenos
CGS 21680 HCl( IC50=22 nM), an adenosine receptor agonist, exhibits 140-fold potency in A2 receptor over A1 receptor.
价 格:¥电议型 号:T6441产 地:中国大陆
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TN1416Ayaninhypertension,airway hyperresponsiveness,Phosphodiesterase (PDE),Inhibitor,inhibit,respiratory
Ayanin has vasorelaxant activity, it also may have the potential for use in treating allergic asthma. The IC50 value of Ayanin is 2.2microM for inhibiting interleukin IL-4 production from purified basophils. Ayanin is a non-selective phosphodiesterase1-4 inhibitor and can be used for respiratory disease researches.
价 格:¥电议型 号:TN1416产 地:中国大陆
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T101645,6-Dihydroxyindole
5,6-Dihydroxyindole is a melanin precursor and has a broad-spectrum antibacterial, antiviral, antifungal, antiparasitic activity. It has cytotoxic effects and is strongly toxic against various pathogens.
价 格:¥电议型 号:T10164产 地:中国大陆
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TN1675Gardenin BGardenin B,Apoptosis,inhibit,Inhibitor
Gardenin B exhibits superior antiproliferative activity against lung, breast, colon, hepatic and leukaemia cell lines as well as in keratinocytes .
价 格:¥电议型 号:TN1675产 地:中国大陆
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T101695-HT4 antagonist 1inhibit,5-HT4 antagonist 1,5-hydroxytryptamine Receptor,Serotonin Receptor,5-HT Re
5-HT4 antagonist 1 is an antagonist of 5-HT4 (pKi = 9.6).
价 格:¥电议型 号:T10169产 地:中国大陆
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TN119216-Epivoacarpine16-Epivoacarpine,Inhibitor,16 Epivoacarpine,16Epivoacarpine,inhibit
16-Epivoacarpine is a natural product from Gelsemium elegans.
价 格:¥电议型 号:TN1192产 地:中国大陆
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T9168NSC 617145NSC 617145,breaks,NHEJ,helicase,DSB,abnormalities,WRN,DNA/RNA Synthesis,strand,Rad51,chrom
NSC617145 is an inhibitor of WRN helicase that inhibits the ATPase, but not exonuclease, activity of WRN helicase in a concentration-dependent manner.
价 格:¥电议型 号:T9168产 地:中国大陆
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T28165NF-1819
NF-1819 is a potent and selective irreversible MGL (β-lactam-based monoacylglycerol lipase) inhibitor. NF-1819 alleviates symptoms in a MS model in vivo and exhibits analgesic effects in an acute inflammatory pain model in vivo. NF-1819 displays high membrane permeability and brain penetrant.
价 格:¥电议型 号:T28165产 地:中国大陆
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T9980AVJ16AVJ16
AVJ16 as a member of the insulin growth factor 2 mRNA-binding protein family, binds to the mRNA of certain genes to regulate protein translation.
价 格:¥电议型 号:T9980产 地:中国大陆