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：3869205
自主品牌
已选条件
-
T29184YM44778；化合物 T29184YM-44778|||YM 44778；YM-44778|||YM 44778
YM44778 is a NK1-receptor antagonist for treating restless legs syndrome.
价 格：￥电议型 号：T29184产 地：中国大陆
-
T29164WY-47766；化合物 WY-47766OST-766|||WY47766|||WY 47766；OST-766|||WY47766|||WY 47766
WY-47766 (OST-766) is a small molecule proton pump inhibitor that can be used to study postmenopausal osteoporosis.
价 格：￥电议型 号：T29164产 地：中国大陆
-
T29139VU0477886；化合物 T29139VU-0477886|||VU 0477886；VU-0477886|||VU 0477886
VU0477886 is a potent mGlu4 positive allosteric modulator (PAM) with robust efficacy in a standard preclinical Parkinson´s disease model, haloperidol-induced catalepsy (HIC).
价 格：￥电议型 号：T29139产 地：中国大陆
-
T28477PZ-128；化合物 T28477PZ 128；PZ 128
PZ-128, a PAR1 antagonist, is used potentially for the treatment of thrombosis.
价 格：￥电议型 号：T28477产 地：中国大陆
-
T27477GSK366A；化合物 T27477GSK366A
GSK366A is an anti-TB agent against Mycobacterium bovis BCG and Mycobacterium tuberculosis, targeting MmpL3 and inhibiting EchA6.
价 格：￥电议型 号：T27477产 地：中国大陆
-
T26968CCT036477；化合物 T26968CCT 036477|||CCT-036477；CCT 036477|||CCT-036477
CCT036477 is a selective inhibitor of wingless-type MMTV integration site family dependent transcription. CCT036477reduces the transcriptional activity of the T-cell factor and lymphoid enhancer factor transcription factor family at the ?-catenin level.
价 格：￥电议型 号：T26968产 地：中国大陆
-
T26477A-315675；化合物 T26477A 315675；A 315675
A-315675 is a neuramidase inhibitor with anti-infuenza activity.
价 格：￥电议型 号：T26477产 地：中国大陆
-
T26457A 85 4777；化合物 T26457A85-4777|||A 8547777；A85-4777|||A 8547777
A 85 4777, a homoperazine derivative, is an anti-inflammatory agent with nonclassical immunosuppressive properties.
价 格：￥电议型 号：T26457产 地：中国大陆
-
T2632A-1210477；化合物A-1210477A-1210477
A-1210477 is an effective and specific MCL-1 and Bcl-2 inhibitor (Ki/IC50: 0.454/26.2 nM).
价 格：￥电议型 号：T2632产 地：中国大陆
-
T25837MRS-1477；化合物 T25837MRS-1477
MRS-1477 is used as a TRPV1 positive allosteric modulator (PAM).
价 格：￥电议型 号：T25837产 地：中国大陆
-
T25477GZ4；化合物 T25477GZ 4|||GZ-4；GZ 4|||GZ-4
GZ4 is a Ca2+ currents inhibitor, acting on cell surface channels.
价 格：￥电议型 号：T25477产 地：中国大陆
-
T24779SEN-1269；化合物 T24779SEN-1269
SEN-1269 is an amyloid-β (AB) aggregation inhibitor that acts by blocking Aβ(1-42) aggregation and protecting neuronal cell lines exposed to Aβ(1-42), reducing Aβ oligomer-induced LTP and memory deficits in vivo.
价 格：￥电议型 号：T24779产 地：中国大陆
-
T24778sEH-IN-12；化合物 T24778sEH inhibitor 12|||sEH-inhibitor-12；sEH inhibitor 12|||sEH-inhibitor-12
sEH-IN-12 is an effective inhibitor of the enzyme soluble epoxide hydrolase (sEH).
价 格：￥电议型 号：T24778产 地：中国大陆
-
T24777Sedecamycin；化合物 T24777T-2636A|||T-2636|||Ro 23-0731/000|||NSC 145117；T-2636A|||T-2636|||Ro 23-0731/0
Sedecamycin is a 17-membered macrolide antibiotic. It is used for treating swine dysentery.
价 格：￥电议型 号：T24777产 地：中国大陆
-
T24776Secologanate；化合物 T24776Secologanic Acid；Secologanic Acid
Secologanate is an inhibitor of plant growth.
价 格：￥电议型 号：T24776产 地：中国大陆
-
T24775SD-2590 HCl；化合物 T24775SD2590 HCl|||SD-2590 Hydrochloride|||SD2590 Hydrochloride|||SD 2590 Hydrochlor
SD-2590 HCl is an MMP-2,-3, -9, -8, 13, and -14 inhibitor.
价 格：￥电议型 号：T24775产 地：中国大陆
-
T24774SD-1029；化合物 T24774SD 1029|||NSC371488|||NSC 371488|||NSC-371488；SD 1029|||NSC371488|||NSC 371488|||N
SD-1029 is a cell-permeable JAK2 inhibitor.
价 格：￥电议型 号：T24774产 地：中国大陆
-
T24773SCH-43478；化合物 T24773SCH 43478；SCH 43478
SCH-43478 is a non-nucleoside agent of antiviral. It has an effective and selective activity against herpes simplex virus type 2 (HSV-2).
价 格：￥电议型 号：T24773产 地：中国大陆
-
T24772SCH-351591；化合物 T24772SCH351591|||SCH 351591|||D4396|||D 4396|||D-4396；SCH351591|||SCH 351591|||D4396
SCH-351591 is an orally active inhibitor of phosphodiesterase 4.
价 格：￥电议型 号：T24772产 地：中国大陆
-
T24771SCH-336；化合物SCH-336SCH336|||SCH 336；SCH336|||SCH 336
SCH-336 is a CB2 receptor agonist (Ki-1.8 nM, EC50-2 nM) with effective, selective, and oral activity. SCH-336 is also bioactive against CB1 receptor, and is 100 times more selective to CB2 receptor than CB1. SCH-336 reduced the binding of guanosine 5´ -3-o -(sulfur) triphosphate to the membrane containing hCB, inhibited BaF3/CB2 cell migration, inhibited leukocyte migration in mouse delayed hypersensitivity models, and inhibited antigen-induced pulmonary eosinophilia in mouse allergy mode
价 格：￥电议型 号：T24771产 地：中国大陆
