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产品数:86101
参观次数:3856707
已选条件
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TN1438beta-Amyrin acetateHMG-CoA,betaAmyrin acetate,LDL,Fungal,inhibit,Inhibitor,arthritic,hemolysis,antif
beta-Amyrin acetate inhibits HMG-CoA Reductase (HMGCR) and sEH activity with IC50 of 3.4 μM. beta-Amyrin acetate has anti-inflammatory, antifungal, antioxidant, and anti-hyperlipidemic activities.
价 格:¥电议型 号:TN1438产 地:中国大陆
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TQ0015PRN1371inhibit,CSF1R,PRN 1371,Inhibitor,colony stimulating factor 1 receptor,c-Fms,CSF-1R,FGFR,CSF-1
PRN1371 is a specific and potent FGFR1-4 and CSF1R inhibitor (IC50s: 0.6/1.3/4.1/19.3/8.1 nM for FGFR1/2/3/4 and CSF1R).
价 格:¥电议型 号:TQ0015产 地:中国大陆
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T38163ML-148ML-148,ML 148,selective,Inhibitor,prostaglandin-signaling,15-PGDH,15-Hydroxyprostaglandin dehy
ML-148 is a selective inhibitor of 15-hydroxy prostaglandin dehydrogenase (15-PGDH, IC50 = 56 nM). ML-148 can be used to profile across a panel of related dehydrogenase or reductase enzymes and in studies about prostaglandin-signaling pathways.
价 格:¥电议型 号:T38163产 地:中国大陆
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T60072ZL0590non-KAc binding site,ZL0590,ZL-0590,BRD4 BD1,Inhibitor,acute airway inflammation,inhibit,Epige
ZL0590 is an effective and selective inhibitor of BD1-BRD4 (IC50 = 90 nM) with anti-inflammatory activities.
价 格:¥电议型 号:T60072产 地:中国大陆
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TN1019Beta-mangostinBeta mangostin,Bacterial,pathway,Apoptosis,carcinoma,migration,antibacterial,inhibit,c
Beta-Mangostin (β-Mangostin) is a xanthone compound with antibacterial and antimalarial activities. Beta-Mangostin (β-Mangostin) present in Cratoxylum arborescens and exhibits antimycobacterial activity against Mycobacterium tuberculosis with an MIC of 6.25 μg/mL. Beta-Mangostin possesses in vitro antimalarial activity against Plasmodium falciparum, with an IC50 of 3.00 μg/mL. beta-Mangostin has potent anticancer activity against various cancers (such as hepatocellular carcinoma, leukaemic).
价 格:¥电议型 号:TN1019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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T8418DCLK1-IN-1DCLK1 IN 1,signaling,PDAC,KRAS,cancer,low,ERK,Inhibitor,selective,DCLK1IN1,inhibit,DCLK-1-
DCLK1-IN-1 is a selective and in vivo-compatible chemical probe of the DCLK1 kinase domain .
价 格:¥电议型 号:T8418产 地:中国大陆
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TWS1293Angelic anhydrideAngelic anhydride,Inhibitor,inhibit
Angelic Anhydride is a reagent in the improved synthesis of angelate esters, which are the active chemical behind the strong pain-relieving and spasmolytic action of extracts from the plant butterbur.
价 格:¥电议型 号:TWS1293产 地:中国大陆
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TJS03145,7-Dihydroxy-4-methylcoumarinBacterial,inhibit,Fungal,Inhibitor,5,7Dihydroxy4methylcoumarin,5,7 Dih
5,7-Dihydroxy-4-methylcoumarin inhibits human neutrophil oxidative metabolism and elastase activity. 5,7-Dihydroxy-4-methylcoumarin has in vitro platelet antiaggregatory property. 5,7-Dihydroxy-4-methylcoumarin shows inhibition of the cyclooxygenase pathway.
价 格:¥电议型 号:TJS0314产 地:中国大陆
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TN1569DeoxylapacholDeoxylapachol,Fungal,inhibit,Inhibitor
Deoxylapachol has anti-wood rot activity, it can inhibit the brown rot fungi Gloeophyllum sepiarium CBS 353.74 and Gloeophyllum trabeum CBS 318.50 and the white rot fungi Merulius tremellosus CBS 280.73 and Phlebia brevispora CBS 509.92. It also can induce fungal cell wall stress.
价 格:¥电议型 号:TN1569产 地:中国大陆
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TMS0484Episyringaresinol 4’-O-β-D-glncopyranosideinhibit,Inhibitor,Episyringaresinol 4’OβDglncopyranoside,E
1. (-)-Syringaresinol inhibits the proliferation of human promyelocytic HL-6 cells through G(1) arrest and induction of apoptosis, may be a potential chemotherapeutic agent for the treatment of cancer.
价 格:¥电议型 号:TMS0484产 地:中国大陆
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TN1474Caulilexin Cantifungal,inhibit,Caulilexin C,phytoalexin,Inhibitor,Fungal
Caulilexin C shows inhibitory activity on human Acyl CoA: cholesterol transferase I (hACATI) and on human Acyl CoA: cholesterol transferase 2 (hACAT2) at 100 mug/ml.
价 格:¥电议型 号:TN1474产 地:中国大陆
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T4074GSK-872translocation,GSK-872,neurological,HMGB1,Receptor-interacting protein kinases,brain,GSK 872,c
GSK872 (GSK2399872A) is an effective and specific RIP3 kinase inhibitor. It binds RIP3 kinase domain with high affinity (IC50: 1.8 nM) and inhibits kinase activity (IC50: 1.3 nM).
价 格:¥电议型 号:T4074产 地:中国大陆
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T6965RG7112E1 activating enzyme,Inhibitor,RO-5045337,E1/E2/E3 Enzyme,RG7112,Ubiquitin conjugating enzyme,
RG7112 (RO5045337) is an orally bioavailable and selective p53-MDM2 inhibitor.
价 格:¥电议型 号:T6965产 地:中国大陆
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TN2027Oxysanguinarineantimalarial,resistant,Parasite,inhibit,Plasmodium,Oxysanguinarine,falciparum strain,
Oxysanguinarine possesses antiplatelet aggregation activity, it has potential inhibitory properties against the dengue virus.
价 格:¥电议型 号:TN2027产 地:中国大陆
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TN6732Oenothein Bantitumor,HCV,Hepatitis C virus,ellagitannin,antifungal,antioxidant,Bacterial,inhibit,Oen
Oenothein B is a specific inhibitor of poly(ADP-ribose) glycohydrolase. Oenothein B shows antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties.
价 格:¥电议型 号:TN6732产 地:中国大陆
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T6944Thiophanate-MethylThiophanate-Methyl,inhibit,Inhibitor,Thiophanate Methyl,ThiophanateMethyl,Fungal
Thiophanate-Methyl (TM), a methyl benzimidazole carbamate (MBC) fungicide,
价 格:¥电议型 号:T6944产 地:中国大陆
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T9459GR103545Inhibitor,Opioid Receptor,imaging,GR103545,inhibit,κ-OR,GR 103545,κ-opioid receptor,GR-10354
(R)-(-)-GR103545 fumarate is a chemical compound.
价 格:¥电议型 号:T9459产 地:中国大陆
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T6703Tetrahydrozoline hydrochloridecongestion,conjunctival,Beta Receptor,Tetryzoline,Tetrahydrozoline hyd
Tetrahydrozoline HCl is an imidazoline derivative with alpha receptor agonist activity.
价 格:¥电议型 号:T6703产 地:中国大陆
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T8485THIQmutant,MC Receptor,inhibit,THIQ,melanocortin,affinity,activity,erectile,selective,eliciting,Mela
THIQ is a selective melanocortin-4 receptor (MC4R) agonist (hMC4R and rMC4R with IC50 of 1.2 nM and 0.6 nM , respectively).
价 格:¥电议型 号:T8485产 地:中国大陆