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:3238294
已选条件
-
T11154EG01377;化合物 T11154EG01377
EG01377 has antiangiogenic, antimigratory, and antitumor effects.EG01377 is a neuropilin-1 (NRP1) antagonist, with a Kd of 1.32 μM for NRP1-b1, and IC50s of both 609 nM for NRP1-a1 and NRP1-b1, but shows no effect on NRP2.
价 格:¥电议型 号:T11154产 地:中国大陆
-
T11153EG00229;化合物 T11153EG00229
EG00229 is a neuropilin 1 (NRP1) receptor antagonist that selectively inhibits the binding of VEGF-A to the NRP1 b1 domain, achieving this inhibition with an IC50 value of 3 μM. It does not affect the binding of VEGF-A to other receptors, such as VEGFR-1 and VEGFR-2.
价 格:¥电议型 号:T11153产 地:中国大陆
-
T11152Edaravone-d5;化合物 T11152MCI-186 D5;MCI-186 D5
Edaravone, a novel and potent free radical scavenger, effectively prevents MMP-9-related brain hemorrhage in rats treated with tissue plasminogen activator. Its deuterium-labeled variant, Edaravone D5, retains the original compound´s attributes while offering isotopic labeling benefits.
价 格:¥电议型 号:T11152产 地:中国大陆
-
T11151Ecteinascidin-Analog-1;化合物 T11151Ecteinascidin-Analog-1
Ecteinascidins is a family of tetrahydroisoquinoline alkaloids with wide range of antitumor and antimicrobial activities. Ecteinascidin-Analog-1 is a useful intermediate for chemical sythesis of Ecteinascidin analogues.
价 格:¥电议型 号:T11151产 地:中国大陆
-
T11150Ecteinascidin 770;化合物 T11150Ecteinascidine 770|||Et-770;Ecteinascidine 770|||Et-770
Ecteinascidin 770 (ET-770) inhibits U373MG cells and is a 1,2,3, 4-tetrahydroisoquinoline alkaloid with strong anticancer activity.IC50 is 4.83 nM.
价 格:¥电议型 号:T11150产 地:中国大陆
-
T1115Doxylamine succinate;琥珀酸多西拉敏Decapryn;琥珀酸多西拉敏|||Decapryn
Doxylamine Succinate is a pyridine derivate histamine H1 antagonist with pronounced sedative properties. Doxylamine succinate (Decapryn) competitively blocks the histamine H1 receptor and limits the typical allergic and anaphylactic responses, including bronchoconstriction, vasodilation, increased capillary permeability, and spasmodic contraction of the gastrointestinal smooth muscle, caused by actions of histamine on bronchial and gastrointestinal smooth muscles, and on capillaries. This drug a
价 格:¥电议型 号:T1115产 地:中国大陆
-
T11139(E/Z)-BCI;化合物(E/Z)-BCINSC 150117;NSC 150117
(E/Z)-BCI (NSC-150117), a dual-specificity phosphatase 6 (DUSP6) inhibitor with anti-inflammatory properties, reduces LPS-induced inflammatory mediators and ROS production in macrophage cells by activating the Nrf2 signaling axis and inhibiting the NF-κB pathway.
价 格:¥电议型 号:T11139产 地:中国大陆
-
T11115Duocarmycin GA;倍癌霉素 GADuocarmycin GA
Duocarmycin GA, an antibody drug conjugate (ADC) toxin and a DNA alkylating agent, effectively targets and binds in the minor groove of DNA. It is particularly potent against multi-drug resistant cell lines, offering a strategic approach in combating resistance.
价 格:¥电议型 号:T11115产 地:中国大陆
-
T11024DHODH-IN-15;化合物DHODH-IN-15DHODH-IN-15
DHODH-IN-15 is the hydroxyfuran analogue of A771726. DHODH-IN-15 is a dihydroorotate dehydrogenase (DHODH) inhibitor with an IC50 of 11 μM for rat liver DHODH. DHODH-IN-15 can be used for rheumatoid arthritis.
价 格:¥电议型 号:T11024产 地:中国大陆
-
T11015Midaglizole hydrochloride;咪格列唑盐酸盐(±)-DG5128|||(±)-DG5128 hydrochloride|||DG5128 hydrochloride|||DG
Midaglizole hydrochloride ((±)-DG5128) (DG5128) is a preferred α2-adrenoceptor antagonist. Midazolazole hydrochloride (DG5128) has an affinity for α2-adrenoceptor (pKi = 6.28) 7.4 times higher than that of α1-adrenoceptor.
价 格:¥电议型 号:T11015产 地:中国大陆
-
T10998Deriglidole;德格列哚SL 86-0715;SL 86-0715
Deriglidole (SL 86-0715) is a peripheral adrenergic receptor antagonist that is a selective inhibitor of alpha2 receptors. Deriglidole inhibits colistin and Idazoxan but does not show activity against prazosin and rat cortical and human platelet α2-adrenergic receptors.
价 格:¥电议型 号:T10998产 地:中国大陆
-
T10981DCZ0415;化合物DCZ0415DCZ0415
DCZ0415 induces antimyeloma activity in vitro, in vivo and in primary cells of drug-resistant myeloma patients. DCZ0415 is a potent TRIP13 inhibitor that can impair the repair of non-homologous end junctions and inhibit NF-κB activity.
价 格:¥电议型 号:T10981产 地:中国大陆
-
T10952LDabuzalgron HCl;化合物 T10952LR1240|||R-450|||R450|||RO-1151240|||R-1240|||RO1151240;R1240|||R-450|||R4
Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.
价 格:¥电议型 号:T10952L产 地:中国大陆
-
T10952Dabuzalgron;达布扎琼Ro 115-1240;达布扎琼|||Ro 115-1240
Dabuzalgron (Ro 115-1240) is an orally active selective alpha-1A adrenergic receptor agonist used to treat urinary incontinence. Dabuzaron prevents cardiotoxicity caused by doxorubicin by maintaining mitochondrial function.
价 格:¥电议型 号:T10952产 地:中国大陆
-
T1095Sparfloxacin;司帕沙星AT-4140|||PD 131501|||Zagam|||CI-978;AT-4140|||PD 131501|||Zagam|||司帕沙星|||CI-978
Sparfloxacin (CI-978) is a fluoroquinolone antibiotic that inhibits bacterial DNA gyrase, thereby inhibiting DNA replication and transcription.
价 格:¥电议型 号:T1095产 地:中国大陆
-
T10939LL-Cystathionine;L-胱硫醚Cystathionine|||ZINC1532680|||L-(+)-Cystathionine|||Cystathionine, L-;L-胱硫醚|||C
L-Cystathionine (Cystathionine, L-) is a key nonprotein amino acid related to metabolic conditions of sulfur-containing amino acids. L-Cystathionine can be used in studies about cardiovascular protection.
价 格:¥电议型 号:T10939L产 地:中国大陆
-
T10915Cycloguanil D6 Nitrate;化合物 T10915Chlorguanide triazine D6 Nitrate;Chlorguanide triazine D6 Nitrate
Cycloguanil D6 Nitrate is a dihydrofolate reductase inhibitor, deuterium-labeled Cycloguanil.
价 格:¥电议型 号:T10915产 地:中国大陆
-
T10903CWHM-1552;化合物CWHM-1552CWHM-1552
CWHM-1552 is an effective Plasmodium falciparum inhibitor. For the 3D7 and Dd2 strains, the IC50s are 51 nM and 53 nM.
价 格:¥电议型 号:T10903产 地:中国大陆
-
T10884CRAC intermediate 1化合物CRAC intermediate 15-(S)-Fluorowillardiine
CRAC intermediate 1 (5-(S)-Fluorowillardiine) is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.
价 格:¥电议型 号:T10884产 地:中国大陆
-
T10865LCot inhibitor-1 hydrochloride;化合物Cot inhibitor-1盐酸盐Cot inhibitor-1 hydrochloride(915365-57-0 Free ba
Cot inhibitor-1 hydrochloride is an inhibitor of tumor progression loci-2 kinase (IC50 = 28 nM) and inhibits the production of TNF-α in human whole blood (IC50 = 5.7 nM).
价 格:¥电议型 号:T10865L产 地:中国大陆