当前位置:易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型:会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累,可浏览访问
(41-90)良好信誉积累,可接洽商谈
(91+ )优质信誉积累,可持续信赖
易推广会员:5年
最后认证时间:
注册号: 【已认证】
法人代表: 【已认证】
企业类型:生产商 【已认证】
注册资金:人民币万 【已认证】
产品数:86101
参观次数:3768243
已选条件
-
T6946Pimavanserin tartrateInhibitor,Pimavanserin hemitartrate,5-hydroxytryptamine Receptor,ACP-103 hemita
Pimavanserin is an effective and specific serotonin 5-HT2A inverse agonist (pIC50: 8.73), used in the therapy of psychosis associated with Parkinson´s disease.
价 格:¥电议型 号:T6946产 地:中国大陆
-
TN1962Myricetin 3-O-galactosideMyricetin 3 O galactoside,Myricetin 3Ogalactoside
Myricetin 3-O-galactoside has cytotoxicity, antioxidant, anti-genotoxic, antinociceptive and anti-inflammatory effects, the effects are related to peripheral inhibition of nitric oxide synthesis, mainly inducible nitric oxide synthase (iNOS).
价 格:¥电议型 号:TN1962产 地:中国大陆
-
TJS03684-Phenyl-7,8-dihydroxycoumarin4Phenyl7,8dihydroxycoumarin,inhibit,Inhibitor,bronchiectasiss,4 Phenyl
7,8-Dihydroxy-4-phenylcoumarin inhibits the activity of Staphylococcus aureus DNA helicase
价 格:¥电议型 号:TJS0368产 地:中国大陆
-
T21060LNPC 567 acetateNPC 567 acetate
NPC 567 acetate is a bradykinin B2 antagonist and can be used in studies about the treatment of allergic airway disease.
价 格:¥电议型 号:T21060L产 地:中国大陆
-
T9346CVN424penetrant,CVN 424,GPR6,inhibit,orally,CVN424,brain,Inhibitor,Parkinson,CVN-424,disease
CVN424 is a selective and novel GPR6 Inverse agonist effective in models of Parkinson Disease.
价 格:¥电议型 号:T9346产 地:中国大陆
-
T26861BMS-817399BMS 817399
BMS-817399 is an orally active antagonist of CCR1 with IC50s of binding affinity and chemotaxis inhibition potencies and can be used in studies about rheumatoid arthritis.
价 格:¥电议型 号:T26861产 地:中国大陆
-
T8232PEG6-(CH2CO2H)2PEG6 (CH2CO2H)2,PROTAC Linkers,PEG-6-(CH2CO2H)2,PEG6-(CH2CO2H)2,PEG6(CH2CO2H)2,inhibi
PEG6-(CH2CO2H)2 is a symmetric PEG PROTAC linker.
价 格:¥电议型 号:T8232产 地:中国大陆
-
T6828ZL0420inhibit,Epigenetic Reader Domain,(E/Z)-ZL0420,BRD4,airway inflammation,immune response genes,Z
ZL0420 is a potent and selective bromodomain-containing protein 4 ( BRD4 ) inhibitor with nanomolar binding affinities to bromodomains (BDs) of BRD4. ZL0420 has IC 50 values of 27 nM against BRD4 BD1 and 32 nM against BRD4 BD2.
价 格:¥电议型 号:T6828产 地:中国大陆
-
T60093CHEMBL1380345
CHEMBL1380345 exhibits antibacterial activity against Staphylococcus aureus, Bacillus cereus, and Escherichia coli with pMIC values of 3.64, 3.56, and 3.70, respectively.
价 格:¥电议型 号:T60093产 地:中国大陆
-
T60108PDGFR Tyrosine Kinase Inhibitor III
PDGFR Tyrosine Kinase Inhibitor III (PDGF Receptor Tyrosine Kinase Inhibitor III) is a multikinase inhibitor that inhibits PDGFR, EGFR, FGFR, PKA, and PKC, respectively. PDGFR Tyrosine Kinase Inhibitor III can be used for the research of amyotrophic lateral sclerosis [1].
价 格:¥电议型 号:T60108产 地:中国大陆
-
T26815BILB-1941
BILB-1941 is an inhibitor of HCV NS5B polymerase and can be used in studies about HCV infection.
价 格:¥电议型 号:T26815产 地:中国大陆
-
T6670Silymarinthistle,angiogenesis,Inhibitor,hepatocellular,resistance,SARS coronavirus,chemopreventive,i
Silymarin (Silybin B) is a polyphenolic flavonoid that extracts from the milk thistle or seeds of Silybum marianum. It is used in the prevention and treatment of liver diseases.
价 格:¥电议型 号:T6670产 地:中国大陆
-
TN2376Fructo-oligosaccharide DP8/GF7inhibit,Fructo oligosaccharide DP8/GF7,Fructooligosaccharide DP8/GF7,F
Fructo-oligosaccharide DP8 / GF7 belongs to fructooligosaccharides (FOS) with degree of polymerization (DP=8). Fructo-oligosaccharides (FOS) are composed of 7 fructose units linked by (2→1)-β-glycosidic bonds and having a single D-glucosyl unit at the non-reducing end.
价 格:¥电议型 号:TN2376产 地:中国大陆
-
TL0016SulforapheneInhibitor,Sulforaphene,ERK,NF-κB,Nuclear factor-κB,Nuclear factor-kappaB,Extracellular s
Sulforaphene is a natural product isolated from radish seeds, exhibits an ED50 against velvetleaf seedlings approximately 2 x 10 -4 M. Sulforaphene promotes cancer cells apoptosis and inhibits migration via inhibiting EGFR, p-ERK1/2, NF‐κB and other signals.
价 格:¥电议型 号:TL0016产 地:中国大陆
-
T7563NBI-98782NBI 98782,NBI-98782,NBI98782,Monoamine Transporter,Inhibitor,inhibit
NBI-98782 is an inhibtior of vesicular monoamine transporter (VMAT2) (Ki: 0.97 nM)
价 格:¥电议型 号:T7563产 地:中国大陆
-
T6947PiperlongumineExtracellular signal regulated kinases,Ferroptosis,Bacterial,Inhibitor,inhibit,Apoptos
Piperlongumine is a natural alkaloid from Piper longum L. It selectively kills cancer cells and strengthens the level of reactive oxygen species (ROS).
价 格:¥电议型 号:T6947产 地:中国大陆
-
TN11468-?Prenylnaringenininhibit,Apoptosis,8?Prenylnaringenin,8-?Prenylnaringenin,Inhibitor,8 ?Prenylnarin
8-Prenylnaringenin is a phytoestrogen with high estrogenic activity,
价 格:¥电议型 号:TN1146产 地:中国大陆
-
T9167PF-9363CTx-648,cancer,patient-derived,anti-tumor,HAT,CTx648,Inhibitor,HATs,selective,xenograft,CTx 6
PF-9363 is a potent and high selective KAT6A/KAT6B inhibitor. PF-9363 can be used for the research of cancer.
价 格:¥电议型 号:T9167产 地:中国大陆
-
T4846BenzylamineBenzylamine
价 格:¥电议型 号:T4846产 地:中国大陆
-
T6686Sulconazole mononitrateanaerobes,antimicrobial,Inhibitor,Fungal,antibacterial,Bacterial,Gram-positiv
Sulconazole Nitrate is the nitrate salt form of sulconazole, a synthetic imidazole derivative with the antifungal property. Sulconazole nitrate inhibits fungal cytochrome P-450 sterol C-14 alpha-demethylation, resulting in the accumulation of fungal 14 alpha-methyl sterols and inhibition of the synthesis of ergosterol, an important component of the fungal cell membrane. Inhibition of ergosterol synthesis leads to a disruption of cell membrane permeability, and ultimately inhibition of cell wall
价 格:¥电议型 号:T6686产 地:中国大陆