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
工商认证 【已认证】
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：3260110
自主品牌
已选条件
-
T70719MLAF50；化合物 MLAF50MLAF50
MLAF50 is an inhibitor of the REV1 UBM2-Ubiquitin interaction.
价 格：￥电议型 号：T70719产 地：中国大陆
-
T70476SML-10-70-1；化合物 SML-10-70-1SML-10-70-1
SML-10-70-1 is a Novel Active Site Inhibitor of Oncogenic K-Ras G12C.
价 格：￥电议型 号：T70476产 地：中国大陆
-
-
T69913Lenumlostat；化合物LenumlostatPAT-1251|||GB2064；PAT-1251|||GB2064
Lenumlostat is an orally available, selective and potent lysyl oxidase-like protein 2 (LOXL2) inhibitor with inhibitory effects on hLOXL2, hLOXL3 and LOXL2 for the study of fibrotic diseases.
价 格：￥电议型 号：T69913产 地：中国大陆
-
T69910EML631；化合物 EML631EML631
EML631 is a potent and selective SPIN1 inhibitor (SPIN1 Kd= 3 microM).
价 格：￥电议型 号：T69910产 地：中国大陆
-
T69907EML-405；化合物 EML-405EML-405
EML-405 is a small-molecule inhibitor of SPIN1 ( Kd of 14 uM).
价 格：￥电议型 号：T69907产 地：中国大陆
-
T69629M?89 MLL inhibitor；化合物 M?89 MLL inhibitorM?89 MLL inhibitor
M?89 is a Highly Potent Inhibitor of the Menin-Mixed Lineage Leukemia (Menin-MLL) Protein?Protein Interaction (Kd = 1.4 nM; IC50 = 25nM). M-89 binds to menin with a Kd value of 1.4 nM and effectively engages cellular menin protein at low nanomolar concentrations. M-89 inhibits cell growth in the MV4;11 and MOLM-13 leukemia cell lines carrying MLL fusion with IC50 values of 25 and 55 nM, respectively, and demonstrates >100-fold selectivity over the HL-60 leukemia cell line lacking MLL fusion.
价 格：￥电议型 号：T69629产 地：中国大陆
-
T69396MLS000108969；化合物 MLS000108969MLS000108969
MLS000108969 is a novel inhibitor of human cytomegalovirus.
价 格：￥电议型 号：T69396产 地：中国大陆
-
T69163BML277 Acid；化合物 BML277 AcidBML277 Acid
BML277 Acid is a metabolite of BML277 which is a selective checkpoint kinase 2 inhibitor.
价 格：￥电议型 号：T69163产 地：中国大陆
-
T69048ML-236C；化合物 ML-236CML-236C
ML-236C is an inhibitor of cholesterogenesis.
价 格：￥电议型 号：T69048产 地：中国大陆
-
T69047ML-236A；化合物 ML-236AML-236A
ML-236A is an inhibitor of cholesterogenesis.
价 格：￥电议型 号：T69047产 地：中国大陆
-
T6896Tolimidone；托利咪酮NSC 314335|||MLR-1023|||CP-26154；托利咪酮|||NSC 314335|||MLR-1023|||CP-26154
Tolimidone (NSC 314335) is a chemical compound which inhibits acid secretion in animal models and also acts as a bronchodilator in histamine-challenged animals.
价 格：￥电议型 号：T6896产 地：中国大陆
-
T6895TAK-580；化合物MLN2480MLN2480|||BIIB-024；MLN2480|||BIIB-024
TAK-580 (MLN2480) is an oral, selective pan-Raf kinase inhibitor in Clinicalal trials.
价 格：￥电议型 号：T6895产 地：中国大陆
-
T6894ML264；化合物ML264CID-51003603；CID-51003603
ML264 (CID-51003603) is a selective kruppel-like factor 5 (KLF5) inhibitor, which potently Inhibits growth of Colorectal Cancer.
价 格：￥电议型 号：T6894产 地：中国大陆
-
T68558BML-288；化合物 BML-288BML-288
BML-288 is a phosphodiesterase Type II (PDE2) inhibitor that demonstrates no inhibition of 5-lipoxygenase (5-LO) or cyclooxygenase (COX-1).
价 格：￥电议型 号：T68558产 地：中国大陆
-
T68489MLN8054 sodium；化合物 MLN8054 sodiumMLN8054 sodium
MLN8054 sodium is an Aurora A inhibitor.
价 格：￥电议型 号：T68489产 地：中国大陆
-
T68427MLN-3897 citrate；化合物 MLN-3897 citrateMLN-3897 citrate
MLN-3897 citrate is a C-C Motif Chemokine Receptor 1 (CCR1) antagonist potentially for the treatment of multiple sclerosis and rheumatoid arthritis.
价 格：￥电议型 号：T68427产 地：中国大陆
-
T68367Amlodipine orotate；化合物 Amlodipine orotateAmlodipine orotate
Amlodipine orotate is a medication used to lower blood pressure and prevent chest pain. It belongs to a group of medications known as dihydropyridine-type calcium channel blockers. By widening of blood vessels it lowers blood pressure. In angina, amlodipine increases blood flow to the heart muscle to relieve pain due to angina.
价 格：￥电议型 号：T68367产 地：中国大陆
-
T67917ML353；化合物ML353VU0478006；VU0478006
ML353 (VU0478006) is a selective activator of TREK-1 and TREK-2 and a selective ligand (Ki =18.2 nM) for the mGlu5 Silencing Allosteric Modulator (SAM). ML353 has potential as a solution to the intrinsic activity or pharmacological blockade of SAM in vivo.
价 格：￥电议型 号：T67917产 地：中国大陆
-
T67885Camlipixant；化合物CamlipixantBLU-5937；BLU-5937
Camlipixant (BLU-5937) is an orally active purine P2X3 receptor antagonist that is potent, selective and competitive. camlipixant has an IC50 of 25 nM for the hP2X3 homotrimer. camlipixant can be used for the treatment of respiratory disorders and Camlipixant has a strong cough suppressant effect.
价 格：￥电议型 号：T67885产 地：中国大陆
