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:3503306
已选条件
-
T60146USP8-IN-1USP8inhibitor
USP8-IN-1 is an inhibitor of USP8 with an IC 50 of 1.9 μM. USP8-IN-1 inhibits H1975 cell growth with a GI 50 of 82.04 μM [1].
价 格:¥电议型 号:T60146产 地:中国大陆
-
T60032BRM/BRG1 ATP Inhibitor-2Epigenetic Reader Domain,Inhibitor,BRM/BRG1 ATP Inhibitor 2,inhibit,BRM/BRG1
BRM/BRG1 ATP Inhibitor-2 is an inhibitor of BRG1/BRM ATPase and can be used in studies about the treatment of BAF-related disorders.
价 格:¥电议型 号:T60032产 地:中国大陆
-
T7815LAOD9604 acetate(221231-10-3 free base)AOD9604 acetate(221231103 free base),AOD-9604 acetate(221231-1
AOD9604 acetate is a potential anti-obesity peptide based on the human growth hormone.
价 格:¥电议型 号:T7815L产 地:中国大陆
-
T60057WAY-388657WAY 388657,WAY388657
WAY-388657 is a Notum Pectinacetylesterase inhibitor with IC50 < 0.025 μM.
价 格:¥电议型 号:T60057产 地:中国大陆
-
T60199NCRW0005-F05NCRW0005F05
NCRW0005-F05 is a potent agonist of orphan G-protein coupled receptor GPR139 with an IC 50 value of 0.21 μM. NCRW0005-F05 can be used to research diabetes, obesity and Parkinson´s disease [1].
价 格:¥电议型 号:T60199产 地:中国大陆
-
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
-
TP1260[Pyr1]-Apelin-13inhibit,[Pyr1]Apelin13,[Pyr1] Apelin 13,Inhibitor,[Pyr-1]-Apelin-13
[Pyr1]-Apelin-13 is a potent and selective endogenous Apelin receptor (APJ) agonist.
价 格:¥电议型 号:TP1260产 地:中国大陆
-
T8980SGA360inhibit,Inhibitor,SGA360,SGA 360,SGA-360
SGA360 is a selective aryl hydrocarbon (Ah) receptor modulator. It exhibits anti-inflammatory properties.
价 格:¥电议型 号:T8980产 地:中国大陆
-
T14550BETd-260
BETd-260, a PROTAC linked by a Cereblon ligand and a BET ligand, has an inhibitory effect on BRD4 protein in leukemic cell lines.
价 格:¥电议型 号:T14550产 地:中国大陆
-
T80605-Bromouracil5 Bromouracil,5Bromouracil
5-Bromouracil disrupts nucleosome positioning by inducing A-form-like DNA.
价 格:¥电议型 号:T8060产 地:中国大陆
-
T8604FenaclonFenaclon
Fenaclon is an anticonvulsant. It is indicated for the treatment of epilepsy.
价 格:¥电议型 号:T8604产 地:中国大陆
-
TP1606LNLS PKKKRKV acetate(95088-49-6 free base)NLS PKKKRKV acetate(95088 49 6 free base),NLS PKKKRKV ace
NLS PKKKRKV acetate is a peptide derived from the 40 tumor antigen of the great ape virus (SV40 big T antigen), which is a method to enhance the nuclear portal in the research field of gene transfer.
价 格:¥电议型 号:TP1606L产 地:中国大陆
-
T38605NCT-504NCT 504,NCT504
NCT-504 is a selective allosteric inhibitor of PIP4Kγ , with an IC 50 of 15.8 μM. NCT-504 is potential for the research of Huntington´s disease.
价 格:¥电议型 号:T38605产 地:中国大陆
-
T60152AZ5576AZ5576
AZ5576 is a potent and highly selective CDK9 inhibitor. AZ5576 can be used for the research of Hematological Malignancy [1].
价 格:¥电议型 号:T60152产 地:中国大陆
-
T9975GPR183GPR183 antagonist-1,SAE-14,inhibit,SAE 14,SAE14,HL-60,GPR183,Inhibitor,GPR183 antagonist SAE-1
GPR183 is a chemotactic receptor known for its role in the maturation of B cells, and the endogenous ligand is the oxysterol 7α,25-dihydroxycholesterol (7α,25-OHC). GPR183 can be used in research on inflammatory bowel disease (IBD).
价 格:¥电议型 号:T9975产 地:中国大陆
-
T60080TMPHneurol disorder,nAChR,Nicotinic acetylcholine receptors,neuronal nicotinic receptors,selective i
TMPH is an inhibitor of nAChR and inhibits nAChRs lacking α5, α6, or β3 subunits. TMPH can be used in studies about nAChR dysfunction or neurological disorders.
价 格:¥电议型 号:T60080产 地:中国大陆
-
T64351GI-560192
GI-560192 is a potent smo cilial modulator with an EC50 value of 0.02 ?M. GI-560192 modulates the translocation and/or accumulation of smoothened to the primary cilia by hedgehog signaling pathway.
价 格:¥电议型 号:T64351产 地:中国大陆
-
TN66602-Ethylhexyl trans-4-methoxycinnamate2Ethylhexyl trans4methoxycinnamate,2 Ethylhexyl trans 4 methoxy
2-Ethylhexyl trans-4-methoxycinnamate is a sunscreen agent.
价 格:¥电议型 号:TN6660产 地:中国大陆
-
T60889RP-6306
RP-6306 is a potent, selective and orally active PKMYT1 inhibitor (IC50= 14 nM). RP-6306 exhibits a high degree of selectivity for PKMYT1 over other kinases in cellular binding assays. RP-6306 exhibits anticancer effects.
价 格:¥电议型 号:T60889产 地:中国大陆
-
TN3609Catalposide
Catalposide is a potent inducer of (HO)-1 isolated from Catalpa ovate G. Don (Bignoniaceae). Catalposide possesses antioxidant, anti-apoptotic, anti-microbial, anti-tumoral, and anti-inflammatory properties.
价 格:¥电议型 号:TN3609产 地:中国大陆