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:3737476
已选条件
-
T93673-(Trifluoromethyl)benzaldehyde3(Trifluoromethyl)benzaldehyde,3 (Trifluoromethyl)benzaldehyde
3-(Trifluoromethyl)benzaldehyde is a chemical compound.
价 格:¥电议型 号:T9367产 地:中国大陆
-
T6S1930SchisanhenolInhibitor,Schisanhenol,inhibit
1. Schisanhenol can protect against adriamycin induced heart mitochondrial toxicity. 2. Schisanhenol has antioxidative effect on human LDL oxidation, may be through scavenging free radicals. 3. Schisanhenol has anti-apoptosis effect on BACSs, may be related to its inhibition of ROS generation.
价 格:¥电议型 号:T6S1930产 地:中国大陆
-
T8851I3MT-3EA.hy926 cells,Hippo (MST),inhibit,I3MT-3,3MST,HEK293,I3MT3,cell-membrane,COS-7,I-3MT-3,I3MT 3
I3MT-3 (HMPSNE) is a potent, selective and cell membrane permeability inhibitor of 3-mercaptopyruvate sulfur transferase (3MST), which targets the persulfated cysteine residues located at the active site of 3MST.
价 格:¥电议型 号:T8851产 地:中国大陆
-
T6934PexmetinibAutophagy,p38 MAPK,ARRY 614,Pexmetinib,Inhibitor,ARRY614,inhibit
Pexmetinib (ARRY-614) is a potent, orally bioavailable, dual p38 MAPK/Tie-2 inhibitor with IC50 of 4 nM/18 nM in a HEK-293 cell line. Phase 1.
价 格:¥电议型 号:T6934产 地:中国大陆
-
T60031NRX-1933inhibit,NRX-1933,NRX1933,Inhibitor,NRX 1933
NRX-1933 is a molecular glue and enhances the interaction between an oncogenic transcription factor, β-Catenin, and its cognate E3 ligase, SCFβ-TrCP.
价 格:¥电议型 号:T60031产 地:中国大陆
-
T9310Urea, N-[4-[4-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-N’-3-pyridinyl-
Urea, N-[4-[4-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)thieno[3,2-d]pyrimidin-2-yl]phenyl]-N´-3-pyridinyl- is a selective mTOR inhibitor with IC50 of 0.29nM and 119nM for mTOR and PI3Kα, respectively.
价 格:¥电议型 号:T9310产 地:中国大陆
-
TP1937L1RFRP-1 (human) acetate(311309-25-8 free base)RFRP1 (human) acetate(311309258 free base),RFRP 1 (huma
RFRP-1 (human) acetate is a potent endogenous NPFF receptor agonist (EC50 values are 0.0011 and 29 nM for NPFF2 and NPFF1, respectively). Attenuates contractile function of isolated rat and rabbit cardiac myocytes. Reduces heart rate, stroke volume, ejection fraction and cardiac output, and increases plasma prolactin levels in rats. GnIH homolog.
价 格:¥电议型 号:TP1937L1产 地:中国大陆
-
T7939FingolimodLPL Receptor,Inhibitor,FTY 720,inhibit,PAK,FTY720,Fingolimod,Lysophospholipid Receptor,p21
Fingolimod is an antagonist of sphingosine 1-phosphate (S1P) (IC50 of 0.033 nM in K562 and NK cells).
价 格:¥电议型 号:T7939产 地:中国大陆
-
T6893MK-886leukotriene,FLAP,5-LOX,5-LO activating protein,non-competitive,L-663536,L663536,keratin-1,Leuk
MK-886 is an inhibitor of leukotriene biosynthesis, inhibiting 5-lipoxygenase-activating protein (FLAP). It is also a moderately potent PPARα antagonist.
价 格:¥电议型 号:T6893产 地:中国大陆
-
T19337GBR 12783 dihydrochloride
GBR 12783 dihydrochloride is a specific, potent and selective dopamine uptake inhibitor. GBR 12783 dihydrochloride inhibits the [3H]dopamine uptake by rat and mice striatal synaptosomes with IC50s of 1.8 nM and 1.2 nM, respectively.GBR 12783 dihydrochloride can improve memory performance and increase hippocampal acetylcholine release in rats.
价 格:¥电议型 号:T19337产 地:中国大陆
-
TQ0068NVP-LCQ195NVP-LCQ195,AT-9311,NVPLCQ195,NVP-LCQ-195,inhibit,Cyclin dependent kinase,Inhibitor,AT 9311
NVP-LCQ195 (AT9311) is a potent inhibitor of CDK1, CDK2, CDK3 and CDK5 (IC50: 1-42 nM).
价 格:¥电议型 号:TQ0068产 地:中国大陆
-
T6518GossypolInhibitor,BL-193,BL193,Gossypol,Bcl-2 Family,inhibit
Gossypol Acetate is a polyphenolic aldehyde that permeates cells and acts as an inhibitor for several dehydrogenase enzymes.
价 格:¥电议型 号:T6518产 地:中国大陆
-
T93542,4-Difluorobenzaldehyde2,4 Difluorobenzaldehyde,2,4Difluorobenzaldehyde
2,4-Difluorobenzaldehyde target bont - botulinum neurotoxin type A (Clostridium botulinum)
价 格:¥电议型 号:T9354产 地:中国大陆
-
T7193Enceniclineinhibit,nAChR,Encenicline,EVP 6124,Nicotinic acetylcholine receptors,EVP6124,Inhibitor
Encenicline is a selective α7 nicotinic acetylcholine receptor (nAChRs) agonist in development for treating cognitive impairment in schizophrenia and Alzheimer´s disease.
价 格:¥电议型 号:T7193产 地:中国大陆
-
TP1933R715 TFA(185052-09-9 free base)R715 TFA(185052 09 9 free base),R715 TFA(185052099 free base),R-715 T
Potent and selective bradykinin B1 receptor antagonist (pA2 = 8.49). Displays no activity at B2 receptors. Reduces mechanical hypernociception in a mouse model of neuropathic pain. Metabolically stable.
价 格:¥电议型 号:TP1933产 地:中国大陆
-
TN4893Rapanoneantioxidant,anti-inflammatory,Bacterial,inhibit,anti-tumor,Phospholipase,antiparasiti,synovi
Rapanone is a natural benzoquinone that is a potent and selective inhibitor of human synovial PLA2.
价 格:¥电议型 号:TN4893产 地:中国大陆
-
T9339Stafia-1Stafia1,domain,Inhibitor,STAT,selectivity,leukemia,inhibit,cells,Stafia 1,Stafia-1,SH2
Stafia-1 is a potent STAT5a inhibitor ( IC50=22.2 μM). Stafia-1 displays high selectivity over STAT5b and other STAT family members.
价 格:¥电议型 号:T9339产 地:中国大陆
-
T7938QuinidineMES-SA,Inhibitor,CYPs,Potassium Channel,Parasite,Cytochrome P450,MESSA/DX5,Apoptosis,oral a
Quinidine is a stereoisomer of the antimalarial agent quinine and a class Ia antiarrhythmic agent. for the treatment of abnormal heart rhythms and also malaria.
价 格:¥电议型 号:T7938产 地:中国大陆
-
T9329BRD0639BRD0639,BRD-0639
BRD0639 is a first-in-class inhibitor of the PRMT5-substrate adaptor interaction. BRD0639 is a PRMT5 binding motif (PBM)-competitive inhibitor that can support studies of PBM dependent PRMT5 activities [1].
价 格:¥电议型 号:T9329产 地:中国大陆
-
T9304(S)-SunvozertinibHER1,Her2,(S)Sunvozertinib,mutant forms of ErbB,Epidermal growth factor receptor,(S
DZD9008 is a rationally designed selective, irreversible EGFR/HER2 inhibitor.
价 格:¥电议型 号:T9304产 地:中国大陆