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：3730798
自主品牌
已选条件
-
T80493?-Conotoxin BuIIIA；化合物 ?-Conotoxin BuIIIA?-Conotoxin BuIIIA
μ-Conotoxin BuIIIA (Mu-Conotoxin BuIIIA), a toxin derived from Cone snail venom, functions as a voltage-gated sodium channel (VGSC) blocker. This toxic peptide is utilized in researching neurological diseases [1].
价 格：￥电议型 号：T80493产 地：中国大陆
-
T80488?-Conotoxin SIIIA；化合物 ?-Conotoxin SIIIA?-Conotoxin SIIIA
μ-Conotoxin SIIIA, a tetrodotoxin (TTX)-resistant sodium channel blocker, is a toxic peptide derived from Conus snail venom. It has applications in researching neurological diseases, including neuropathic pain [1].
价 格：￥电议型 号：T80488产 地：中国大陆
-
T80459ω-Conotoxin CnVIIA；化合物 ω-Conotoxin CnVIIAω-Conotoxin CnVIIA
ω-Conotoxin CnVIIA, a 27-amino-acid neuropeptide toxin, serves as an N-type calcium current blocker [1].
价 格：￥电议型 号：T80459产 地：中国大陆
-
T80230μ-Conotoxin Sx IIIA；化合物 μ-Conotoxin Sx IIIAμ-Conotoxin Sx IIIA
μ-Conotoxin Sx IIIA is a biologically active peptide that functions as a blocker of NaV1.4 channels.
价 格：￥电议型 号：T80230产 地：中国大陆
-
T80163μ-Conotoxin PIIIA；化合物 μ-Conotoxin PIIIAμ-Conotoxin PIIIA
μ-Conotoxin PIIIA, isolated from Conus purpurascens [1] [2], is a blocker of the sodium channel NaV 1.4.
价 格：￥电议型 号：T80163产 地：中国大陆
-
T80162Aah II；化合物 Aah IIAah II
Aah II, a sodium channel modulator, is a toxin derived from the venom of the scorpion Androctonus australis [1] [2].
价 格：￥电议型 号：T80162产 地：中国大陆
-
T80159?-Conotoxin KIIIA；化合物 ?-Conotoxin KIIIA?-Conotoxin KIIIA
μ-Conotoxin KIIIA, an analgesic compound derived from Conus kinoshitai, selectively inhibits mammalian neuronal voltage-gated sodium channels (VGSCs) (Nav1.2), offering potential utility in pain research [1] [2].
价 格：￥电议型 号：T80159产 地：中国大陆
-
T80039ATX-II；化合物 ATX-IIATX-II
ATX-II, an Na+ channel modulator toxin derived from the sea anemone (Anemonia sulcata), causes delayed inactivation of the Na+ channels and has been linked to pulmonary vein arrhythmogenesis and atrial fibrillation [1] [2]. It exhibits interaction with halothane, caffeine, and ryanodine.
价 格：￥电议型 号：T80039产 地：中国大陆
-
T7577Angiotensin III, human, mouse；血管紧张素IIIAngiotensin III, human, mouse(3TFA)；血管紧张素III|||Angiotensin III
Angiotensin III, human, mouse (Angiotensin III, human, mouse(3TFA))(3TFA) is an endogenous angiotensin II receptor (AT2R) agonist(IC50s of 0.648 nM).
价 格：￥电议型 号：T7577产 地：中国大陆
-
T75619Aristololactam IIIa；化合物 Aristololactam IIIaAristololactam IIIa
Aristololactam IIIa demonstrates substantial inhibition of superoxide anion generation and elastase release, exhibiting IC50 values of 0.12 and 0.20 μg/mL, respectively [1].
价 格：￥电议型 号：T75619产 地：中国大陆
-
T75541Tanshinone IIA anhydride；化合物 Tanshinone IIA anhydrideTanshinone IIA anhydride
Tanshinone IIA anhydride is a potent, irreversible inhibitor of human carboxylesterase (CE), exhibiting inhibitory constants (K i values) of 1.9 nM for human CE1 and 1.4 nM for human intestinal CE (hiCE), respectively [1].
价 格：￥电议型 号：T75541产 地：中国大陆
-
T72281Caspase-9 Inhibitor III；化合物 Caspase-9 Inhibitor IIIAc-LEHD-cmk；Ac-LEHD-cmk
Caspase-9 Inhibitor III (Ac-LEHD-cmk), a caspase-9 inhibitor, exhibits protective effects against ischemia-reperfusion-induced myocardial injury.
价 格：￥电议型 号：T72281产 地：中国大陆
-
T67884β-catenin modulator IIa-661；化合物 β-catenin modulator IIa-661β-catenin modulator IIa-661
β-catenin modulator IIa-661 is a small molecule inhibitor of the Wnt pathway with antitumour activity.
价 格：￥电议型 号：T67884产 地：中国大陆
-
T5S0836Isoastragaloside II；黄芪甲苷VIIAstrasieversianin VII；黄芪甲苷VII|||Astrasieversianin VII
Isoastragaloside II (Astrasieversianin VII) is a derivative Astragaloside I, an ingredient in Astragalus membranaceus which is reported to have osteogenic properties.
价 格：￥电议型 号：T5S0836产 地：中国大陆
-
T5S0833Astragaloside III；黄芪皂苷 IIIAstragaloside III
Astragaloside III has cardioprotective effects as well as causing improvement in cognitive function. It can be used in the prevention of cardio-cerebral vascular diseases. It also is antioxidant.
价 格：￥电议型 号：T5S0833产 地：中国大陆
-
T5524Aurora kinase inhibitor-3；化合物Aurora Kinase Inhibitor IIIAurora Kinase Inhibitor III；Aurora Kinase In
Aurora kinase inhibitor-3 (Aurora Kinase Inhibitor III) is a potent inhibitor of Aurora A kinase (IC50 = 42 nM).1 It is selective for Aurora A over BMX, BTK, IGF-1R, c-Src, TRKB, SYK, and EGFR.
价 格：￥电议型 号：T5524产 地：中国大陆
-
T3S1471Cucurbitacin IIA；葫芦素IiaDihydrocucurbitacin Q1|||Hemslecin A|||Curcurbitacin IIA；葫芦素Iia|||Dihydrocucu
1. Cucurbitacin IIA (Dihydrocucurbitacin Q1) can induce apoptosis and enhance autophagy , contributes to the anti-inflammatory activity of Cucurbitacin IIA against inflammation-related diseases. 2. Cucurbitacin IIA is a novel class of anti-cancer drug in suppression of cancer cell expansion by disrupting the actin cytoskeleton and directing the cell to undergo PARP-mediated apoptosis through the inhibition of survivin downstream of JAK2/STAT3.
价 格：￥电议型 号：T3S1471产 地：中国大陆
-
T3924Astragaloside II；黄芪皂苷 IIAstrasieversianin VIII；黄芪皂苷 II|||Astrasieversianin VIII
Astragaloside II (Astrasieversianin VIII) is an effective MDR reversal agent and may be a potential adjunctive agent for hepatic cancer chemotherapy. Astragaloside II also induces osteogenic activities, differentiation, proliferation, and mineralization, through the bone morphogenetic protein-2/MAPK and Smad1/5/8 pathways.
价 格：￥电议型 号：T3924产 地：中国大陆
-
T3346AKT inhibitor VIII；化合物AKT inhibitor VIIIAKTi-1/2；AKTi-1/2
AKT inhibitor VIII (AKTi-1/2) is a highly specific Akt1/2 inhibitor (IC50: 58/210 nM). The selectivity for Akt1 is higher about 36-fold than Akt3.
价 格：￥电议型 号：T3346产 地：中国大陆
-
T2946Tanshinone IIA sulfonate sodium；丹参酮IIA磺酸盐Tanshinone IIA sulfonate|||Sodium Tanshinone IIA sulfonate|
Tanshinone IIA sulfonate sodium (Tanshinone IIA sodium sulfonate) is a water-soluble derivative of tanshinone IIA extracted from Savia miltiorrhiza; a potent negative allosteric modulator of the human purinergic receptor P2X7. Tanshinone IIA sulfonate sodium (12.5 μM) inhibits hypoxia-induced PKG and PPAR-γ downregulation in PASMCs and distal pulmonary arteries of rats.
价 格：￥电议型 号：T2946产 地：中国大陆
