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：3766780
自主品牌
已选条件
-
T3S19579-amino-CPT；9-氨基喜树碱Aminocamptothecin|||9-amino-2(S)-camptothecin|||9-Aminocamptothecin；9-氨基喜树碱|||Ami
9-amino-CPT (Aminocamptothecin) is an inhibitor of topoisomerase I with potent anticancer activity.
价 格：￥电议型 号：T3S1957产 地：中国大陆
-
T3S19557-Ethylcamptothecin；7-乙基喜树碱7-Ethylcamptothecin
1. 7-Ethylcamptothecin has the superior antitumor activity than CPT. (a). 7-Ethylcamptothecin has a stronger growth-inhibiting activity against tumor cells. (b). 7-Ethylcamptothecin remains in the intestinal tract for a longer time and in higher amounts when administered in vivo.
价 格：￥电议型 号：T3S1955产 地：中国大陆
-
T3S0717Thymol；百里酚2-isopropyl-5-methylphenol|||Pseudoaspidin|||Thymic Acid|||Thyme Camphor；2-isopropyl-5-met
Thymol, also known as Pseudoaspidin, is a principal monoterpene phenol found in the essential oils of plants from the Lamiaceae family, along with several other families including Verbenaceae, Scrophulariaceae, Ranunculaceae, and Apiaceae. This compound exhibits antioxidant, anti-inflammatory, antibacterial, and antifungal properties.
价 格：￥电议型 号：T3S0717产 地：中国大陆
-
T39792AMPC；AMPCAMPC
AMPC, a powerful and efficient inhibitor of TFF3, demonstrates inhibitory effects on cell proliferation, survival, oncogenicity, and CSC-like behavior in TFF3-positive CMS4 CRC cells. It acts as a promising standalone anti-cancer agent and also enhances the effects of 5-FU when used in combination, making it a valuable tool for cancer research.
价 格：￥电议型 号：T39792产 地：中国大陆
-
T3957Farampator；化合物FarampatorOrg24448|||CX-691；Org24448|||CX-691
Farampator (CX-691) (CX-691;Org24448) is a positive modulator of AMPA receptor.
价 格：￥电议型 号：T3957产 地：中国大陆
-
T38696Rp-8-CPT-cAMPS；Rp-8-CPT-cAMPSRp-8-CPT-cAMPS
Rp-8-CPT-cAMPS is a powerful and competitive antagonist of cAMP-induced activation of cAMP-dependent protein kinase (PKA) I and II. Acting as a potent cAMP analog, Rp-8-CPT-cAMPS exhibits a preference for site A of RI over site A of RII. Additionally, it favors site B of RII over site B of RI. This compound effectively inhibits cAMP-dependent PKA activation and demonstrates selectivity in binding to specific sites within the protein kinase.
价 格：￥电议型 号：T38696产 地：中国大陆
-
T38694Sp-8-CPT-cAMPS；Sp-8-CPT-cAMPSSp-8-CPT-cAMPS
Sp-8-CPT-cAMPS is a powerful and specific cAMP analog that activates cAMP-dependent protein kinase A (PKA I and PKA II) selectively and effectively. It exhibits a 153-fold preference for site A of RI over site A of RII, and a 59-fold preference for site B of RII over site B of RI.
价 格：￥电议型 号：T38694产 地：中国大陆
-
T38588Amphotericin B trihydrate；两性霉素B三水合物Amphotericin B trihydrate
Amphotericin B trihydrate, a polyene antibiotic, is derived from Streptomyces nodosus fermenter cultures. It exhibits antileishmanial properties.
价 格：￥电议型 号：T38588产 地：中国大陆
-
T37734AMPA receptor modulator-2；化合物AMPA receptor modulator-2AMPA receptor modulator-2
AMPA receptor modulator-2 is a modulator of AMPA receptor. The pIC50 value for TARPγ2 dependent AMPA receptor is 10.1.
价 格：￥电议型 号：T37734产 地：中国大陆
-
T37733AMP-PNP tetralithiumAMP PNPAMP PNP tetralithium|||AMPPNP tetralithium
Non-hydrolyzable AMP analog. Kir6 (KATP) channel blocker. Inhibits fast axonal transport and stabilizes the interaction of membranous organelles with microtubules.
价 格：￥电议型 号：T37733产 地：中国大陆
-
T375252-Methylthio-AMP diTEA；2-Methylthio-AMP diTEA2-Methylthio-AMP diTEA
2-Methylthio-AMP diTEA (2-MeSAMP) is a selective and direct antagonist of the P2Y12 receptor, effectively inhibiting ADP-dependent platelet aggregation[1][2][3].
价 格：￥电议型 号：T37525产 地：中国大陆
-
T36679Rp-cAMPS sodium salt；Rp-cAMPS sodium saltRp-cAMPS sodium salt
Rp-cAMPS sodium salt, a cAMP analog, is a potent, competitive cAMP-induced activation of cAMP-dependent PKA I and II (Kis of 12.5 μM and 4.5 μM, respectively) antagonist. Rp-cAMPS sodium salt is resistant to hydrolysis by phosphodiesterases[1][2][3][4][5][6].
价 格：￥电议型 号：T36679产 地：中国大陆
-
T36678Rp-8-CPT-cAMPS sodium；Rp-8-CPT-Cyclic AMP (sodium salt)Rp-8-CPT-cAMPS sodium
Rp-8-CPT-cAMP is a structural combination of the lipophilic and non-hydrolyzable cAMP analogs, 8-CPT-cyclic AMP and Rp-cyclic AMPS .[1] It functions as a site-selective inhibitor of protein kinase A (PKA) type I and II, with preference towards site A of type I and site B of type II.2 By occupying cAMP binding sites at the regulatory subunit of PKA, Rp-8-CPT-cAMP prevents the kinase holoenzyme from dissociative activation.[2],[3]
价 格：￥电议型 号：T36678产 地：中国大陆
-
T36677Rp-8-bromo-Cyclic AMPS (sodium salt)；Rp-8-bromo-Cyclic AMPS (sodium salt)Rp-8-bromo-Cyclic AMPS (sod
Rp-8-bromo-Cyclic AMPS (Rp-8-bromo-cAMPS) is a cell-permeable cAMP analog that combines an exocyclic sulfur substitution in the equatorial position of the cyclophosphate ring with a bromine substitution in the adenine base of cAMP. It acts as an antagonist of cAMP-dependent protein kinases (PKAs) and is resistant to hydrolysis by cyclic nucleotide phosphodiesterases. Rp-8-bromo-cAMPS more effectively antagonizes cAMP-dependent activation of purified PKA type I from rabbit muscle than PKA type II
价 格：￥电议型 号：T36677产 地：中国大陆
-
T3570625-Desacetyl Rifampicin；25-Desacetyl Rifampicin25-Desacetyl Rifampicin
25-Desacetyl rifampicin is a major active metabolite of the rifamycin antibiotic rifampicin .125-Desacetyl rifampicin is active againstM. smegmatis(MIC99= 2.66 μM).
价 格：￥电议型 号：T35706产 地：中国大陆
-
T35651BromamphenicolBromamphenicolBromamphenicol
Bromamphenicol is a dibrominated derivative of the antibiotic chloramphenicol. It inhibits rat liver mitochondrial and E. coli protein synthesis by 90.6 and 98.8%, respectively, when used at a concentration of 93 μM, and inhibits DNA synthesis in human lymphoblastoid cells by 83% at 1 mM. Bromamphenicol can also bind to the major adhesin subunit DraE from E. coli.
价 格：￥电议型 号：T35651产 地：中国大陆
-
T35626AMP-Deoxynojirimycin；化合物 AMP-DeoxynojirimycinAMP-DNM；AMP-DNM
AMP-Deoxynojirimycin (AMP-DNM) is a potent inhibitor of ceramide glucosyltransferase and GCase 2.AMP-Deoxynojirimycin is a potent inhibitor of GlcCer biosynthesis and is used in the study of Parkinson´s and diabetes.
价 格：￥电议型 号：T35626产 地：中国大陆
-
T35595Cyclic di-AMP (sodium salt)；Cyclic di-AMP (sodium salt)Cyclic di-AMP (sodium salt)
Cyclic di-AMP (c-di-AMP) is a second messenger produced by bacteria but not by mammals. Generated by a family of diadenylate cyclases, c-di-AMP can impact bacterial cell growth, cell wall homeostasis, pathogenicity, and other cellular functions. Bacteria-derived cyclic dinucleotides, including c-di-AMP, trigger the expression of interferon genes in mammalian cells.
价 格：￥电议型 号：T35595产 地：中国大陆
-
T354248-bromo-Cyclic AMP；8-bromo-Cyclic AMP8-bromo-Cyclic AMP
8-bromo-Cyclic AMP is a brominated derivative of cAMP that remains long-acting due to its resistance to degradation by cAMP phosphodiesterase. It can activate cAMP-dependent protein kinase, inhibiting growth, decreasing proliferation, increasing differentiation, and inducing apoptosis of cancer cells.
价 格：￥电议型 号：T35424产 地：中国大陆
-
T35203Xylonidine；化合物 T35203SK&F-35866|||SK&F35866|||SK&F 35866；SK&F-35866|||SK&F35866|
Xylonidine is a biochemical.
价 格：￥电议型 号：T35203产 地：中国大陆
