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：3875470
自主品牌
已选条件
-
T27730KGP94；化合物KGP94KGP-94|||KGP 94；KGP-94|||KGP 94
KGP94 is a potent, selective, and competitive inhibitor of the lysosomal endopeptidase enzyme.
价 格：￥电议型 号：T27730产 地：中国大陆
-
T2773Vindoline文多灵文朵灵|||文多灵
Vindoline is an indole alkaloid that exhibits antimitotic activity by inhibiting microtubule assembly.
价 格：￥电议型 号：T2773产 地：中国大陆
-
T27673JNJ-26990990；化合物JNJ-26990990JNJ-26990990
JNJ-26990990 is a broad-spectrum anticonvulsant drug as a second-generation followup to the marketed drug topiramate. It was designed to have the same anticonvulsant effects as topiramate, but without the side effects associated with topiramate´s carbonic anhydrase inhibition. It also has potential use in the treatment of inflammatory pain, neuropathic pain, and depression. JNJ-26990990 entered phase II clinical trials in October 2007.
价 格：￥电议型 号：T27673产 地：中国大陆
-
T27636Ispronicline；异丙克兰AZD-3480|||RJR-1734|||AZD 3480|||TC 1734|||AZD3480|||TC-01734|||TC-1734-112；AZD-348
Ispronicline (TC-1734) An orally active, selective, and potent α4β2 nAChR partial agonist with antidepressant, neuroprotective, and long-lasting cognitive effects.Ispronicline has a high affinity for the α4β2 nAChR with a Ki= 11 nM.
价 格：￥电议型 号：T27636产 地：中国大陆
-
T27573Ibuproxam；化合物 T27573Ibuproxamum|||G-277；Ibuproxamum|||G-277
Ibuproxam, a nonsteroidal antiinflammatory drug (NSAID), is used for the treatment of musculoskeletal pain, arthritis, and soft-tissue disorders.
价 格：￥电议型 号：T27573产 地：中国大陆
-
T27491GSK730；化合物 T27491GSK730
GSK730 is an inactive enantiomer of GSK729 (GLXC-09258).
价 格：￥电议型 号：T27491产 地：中国大陆
-
T27473GSK334429；化合物 T27473GSK-334429|||GSK 334429；GSK-334429|||GSK 334429
GSK334429 is an antagonist of histamine H3 receptor.
价 格：￥电议型 号：T27473产 地：中国大陆
-
T27472GSK317354A；化合物 T27472GSK 317354A|||GSK-317354A；GSK 317354A|||GSK-317354A
GSK317354A is a GRK2 inhibitor.
价 格：￥电议型 号：T27472产 地：中国大陆
-
T27453GSK1733953A化合物GSK1733953ADG70
GSK1733953A can be used as a small molecule Mycobacterium tuberculosis respiration inhibitor with an inhibitory effect on MenG activity and an IC50 value of 2.6 ± 0.6 μM.GSK1733953A is a selective biphenylbenzamide with an inhibitory effect on the catalytic methylation of the Mycobacterium tuberculosis desmethylnaphthoquinone methyltransferase, and the MIC of GSK1733953A against Mycobacterium tuberculosis H4Rv was 8.37 μg/ml. MIC of 8.37 μg/ml and MIC of 1.2 to 9.6 μg/ml against drug-resistant s
价 格：￥电议型 号：T27453产 地：中国大陆
-
T27399Galocitabine；加洛他滨RO 091390|||RO-091390|||RO091390|||RO-09-1390|||Neofrutulon；RO 091390|||RO-091390||
Galocitabine (Neofrutulon), a thymidylate synthase inhibitor, is used potentially for the treatment of cancer.
价 格：￥电议型 号：T27399产 地：中国大陆
-
T27398Gallium maltolate；麦芽酚镓Gallium maltolate
Gallium maltolate is a ribonucleoside-diphosphate reductase inhibitor.
价 格：￥电议型 号：T27398产 地：中国大陆
-
T27395Furamidine dihydrochloride；化合物 T27395DB 75, DB75, NSC 305831, WR199385|||Furamidine HCl；DB 75, DB75,
Furamidine is a cell-permeable, selective inhibitor of protein arginine methyltransferase 1 (PRMT1). Furamidine binds to strings of AT base pair sequences in DNA′s minor groove. Furamidine targets the enzyme active site and is primarily competitive with the substrate and noncompetitive toward the cofactor. Furthermore, Furamidine blocks cell proliferation in leukemia cell lines with different genetic lesions.
价 格：￥电议型 号：T27395产 地：中国大陆
-
T27394Furalazine；化合物 T27394Furalazinum|||Panfuran|||Nifuralazinum|||NFT；Furalazinum|||Panfuran|||Nifuralaz
Furalazine is an antimicrobial agent. Furalazine was more effective in reducing the duration of positive stool culture than chloramphenicol. It may be potentially used in the treatment of cholera.
价 格：￥电议型 号：T27394产 地：中国大陆
-
T27393FTO-IN-7d；化合物 T27393FTO-IN-7d
FTO-IN-7d is the first inhibitor of the RNA demethylase FTO with anticonvulsant activity.
价 格：￥电议型 号：T27393产 地：中国大陆
-
T27392FT001；化合物FT001FT001
FT001 is a potent, selective and orally available inhibitor of BET Bromodomain with antitumor activity. FT001 inhibited the expression of MYC with the IC50 value of 0.46 μM). FT001 has potent antiproliferative effects against MV-4-11 and demonstrates significant MYC mRNA suppression both in vitro and in vivo.
价 格：￥电议型 号：T27392产 地：中国大陆
-
-
T27390Friulimicin B；化合物 T27390Friulimicin B
Friulimicin B is a peptidoglycan synthesis inhibitor with excellent activity against gram-positive pathogens through cell wall interruption.
价 格：￥电议型 号：T27390产 地：中国大陆
-
T2739Shikimic Acid；莽草酸Shikimate；Shikimate|||莽草酸
Shikimic Acid (Shikimate) is a tri-hydroxy cyclohexene carboxylic acid important in the biosynthesis of so many compounds that the shikimate pathway is named after it.
价 格：￥电议型 号：T2739产 地：中国大陆
-
T27389Frequentin；化合物 T27389Frequentin
Frequentin, an antibiotic originally isolated from P. frequentans, is active against bacteria (MICs = 200 and 300 ?g/ml for B. subtilis and S. aureus, respectively) and fungi.
价 格：￥电议型 号：T27389产 地：中国大陆
-
T27388FR-A 19；化合物 T27388FR-A-19|||FRA19；FR-A-19|||FRA19
FR-A 19, a Histamine H2 agonist, inhibits the release of IgE-mediated human basophil histamine in a nanomolar range. It has additional potent anti-allergic properties.
价 格：￥电议型 号：T27388产 地：中国大陆
