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T7092NADPH tetrasodium salt；还原型辅酶IINADPH tetrasodium salt
NADPH tetrasodium salt is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate, which acts as an electron donor in a variety of biological reactions. NADPH tetrasodium salt is also an endogenous inhibitor of iron death.
价 格：￥电议型 号：T7092产 地：中国大陆
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T70832Bisindolylmaleimide VII；化合物 Bisindolylmaleimide VIIBisindolylmaleimide VII
Bisindolylmaleimide VII is a selective inhibitor of protein kinase C.
价 格：￥电议型 号：T70832产 地：中国大陆
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T7040Angiotensin II human；血管紧张素ⅡDRVYIHPF|||Angiotensin II|||Hypertensin II|||Ang II；DRVYIHPF|||Angiotensi
Angiotensin II human (Ang II) is a biologically active peptide, a vasoconstrictor. Angiotensin II interacts with AT1R and AT2R to regulate blood pressure, stimulate sympathetic nerves, and increase aldosterone biosynthesis and renal activity in humans.
价 格：￥电议型 号：T7040产 地：中国大陆
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T70351VS-II-173；化合物 VS-II-173VS-II-173
VS-II-173 is a novel potent Pim1 and Pim3 inhibitor, selectively inducing AML cell death.
价 格：￥电议型 号：T70351产 地：中国大陆
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T7031Aristolochic acid B；马兜铃酸 BAristolochic Acid II；马兜铃酸B|||Aristolochic Acid II|||马兜铃酸 B
Aristolochic acid B (Aristolochic Acid II) is one of the major components of the carcinogenic plant extract aristolochic acid, is known to be mutagenic and to form DNA adducts in vitro and in vivo, Aristolochic acid B shows more carcinogenic risk than aristolochic acid I, and this may be, at least partly, the result of its increased levels in kidney and plasma.
价 格：￥电议型 号：T7031产 地：中国大陆
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T7009Soyacerebroside II；化合物 T7009Soyacerebroside II
Soyacerebroside II exhibits ionophoretic activity for Ca2+ ion. Soyacerebrosides I and II have modulating the cellular immune response effects, they show obvious inhibitory activity on IL-18 secretion in human peripheral blood mononuclear cells (PBMC).
价 格：￥电议型 号：T7009产 地：中国大陆
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T6S2099Geraniin；老鹳草素Geraniin
1. Geraniin has a protective effect against OVX-induced rat osteoporosis. 2. Geraniin has cytotoxic activity towards cancer cells in vitro and in vivo. 3. Geraniin exerts inhibitory effects on osteoclast differentiation in vitro and suppresses Ti particle-induced osteolysis in vivo, is a potential natural compound for the treatment of wear particle induced osteolysis in prostheses failure. 4. Geraniin has anti-oxidant activity, induces Nrf2-mediated expression of antioxidant enzymes HO-1 and NQO
价 格：￥电议型 号：T6S2099产 地：中国大陆
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T6S2038Ziyuglycoside II；地榆皂苷IIZiyuglycoside II
1. Ziyuglycoside II has anti-inflammation and antioxidation properties. 2. Ziyuglycoside II has antibiosis, and homeostasis properties. 3. Ziyuglycoside II has anticancer, and antitumor properties against gastric cancer and breast cancer cells, by cell cycle arrest and cell apoptosis.
价 格：￥电议型 号：T6S2038产 地：中国大陆
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T6S1688(1E,6E)-Bis(demethoxy)curcumin；双去甲氧基姜黄素Curcumin III|||Didemethoxycurcumin|||BDMC；(1E,6E)-1,7-双(4-羟基苯
(1E,6E)-Bis(demethoxy)curcumin (Curcumin III) is a natural demethoxy derivative of curcumin,with anti-inflammatory and anti-cancer activities.
价 格：￥电议型 号：T6S1688产 地：中国大陆
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T6S1683Demethoxycurcumin；去甲氧基姜黄素Curcumin II|||Desmethoxycurcumin|||Monodemethoxycurcumin；Curcumin II|||去甲氧基
1. Demethoxycurcumin (Desmethoxycurcumin) has antioxidant activity. 2. Demethoxycurcumin has anti-inflammatory activity. 3. Demethoxycurcumin has anti-proliferative activity. 4. Demethoxycurcumin has anti-acanthamoebic effect. 5. Demethoxycurcumin is a potential additive natural product in combination with chemotherapeutic agents in drug-resistant cancers. 6. Demethoxycurcumin inhibits energy metabolic and oncogenic signaling pathways through AMPK activation in triple-negative breast cancer cell
价 格：￥电议型 号：T6S1683产 地：中国大陆
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T6S1543Dehydrodiisoeugenol脱氢二异丁香酚去氢二异丁香酚|||脱氢二异丁香酚
1. Dehydrodiisoeugenol has anti-inflammatory activity. (1). Dehydrodiisoeugenol inhibited the expression of the COX-2 in RAW264.7 murine macrophages stimulated with LPS. (2). Dehydrodiisoeugenol inhibited LPS-stimulated phosphorylation-dependent proteolysis of inhibitor κB-α and transcriptional activity of NF-κB in the cells.
价 格：￥电议型 号：T6S1543产 地：中国大陆
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T6S0653Linarin蒙花苷Buddleoflavonoloside|||Buddleoside|||Acacetin-7-O-rutinoside|||Acaciin|||Linarine|||蒙花苷
1. Linarin (Acacetin-7-O-rutinoside) (acacetin-7-O-β-d-rutinoside) shows selective dose dependent inhibitory effect on acetylcholinesterase. 2. Linarin alleviates GalN/LPS-induced liver injury by suppressing TNF-α-mediated apoptotic pathways. 3. Linarin prevents A beta-induced neurotoxicity through the activation of PI3K/Akt, which subsequently inhibits GSK-3b and up-regulates Bcl-2. 4. The piperine significantly enhanced the oral absorption of Linarin in rats by inhibiting P-glycoprotein mediat
价 格：￥电议型 号：T6S0653产 地：中国大陆
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T6991Nitroprusside disodium dihydrate；硝普钠二水合物Sodium Nitroferricyanide(III) Dihydrate|||Sodium Nitroprussi
Nitroprusside disodium dihydrate (Sodium Nitroprusside Dihydrate) is a potent vasodilator working through releasing NO spontaneously in blood.
价 格：￥电议型 号：T6991产 地：中国大陆
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T69795Crobenetine；克罗奈汀BIII 890 CL|||Crobenetine Free Base；BIII 890 CL|||Crobenetine Free Base
Crobenetine (BIII 890 CL) Free Base is a selective NaV channel blocker that eliminates VTD-induced [Ca2+] elevation.
价 格：￥电议型 号：T69795产 地：中国大陆
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T69621BIIE-0246 HCl；化合物 BIIE-0246 HClBIIE-0246 HCl
BIIE-0246 is a potent, selective and competitive non-peptide antagonist for the neuropeptide Y Y2 receptor. BIIE-0246 displays > 650-fold selectivity over Y1, Y4 and Y5 receptors.
价 格：￥电议型 号：T69621产 地：中国大陆
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T69502HSP47 inhibitor III；化合物 HSP47 inhibitor IIIHSP47 inhibitor III
HSP47 inhibitor III suppressed collagen type I expression in human and mouse cells and suppressed the viability and migration of lung fibroblasts.
价 格：￥电议型 号：T69502产 地：中国大陆
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T6945Vps34-PIK-III；化合物PIK-IIIPIK-III|||VPS34-IN2；PIK-III|||VPS34-IN2
Vps34-PIK-III (VPS34-IN2), a selective inhibitor of VPS34 enzymatic activity, inhibits autophagy and results in the stabilization of autophagy substrates.
价 格：￥电议型 号：T6945产 地：中国大陆
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T69056Albizziin；化合物 AlbizziinAlbizziin
Albizziin is amino acid analog which acts as a competitive inhibitor of asparagine synthetase with respect to glutamine. Albizziin has been used to isolate mutants of Chinese hamster ovary cells with alterations in levels of the target enzyme. Several classes of mutations can be distinguished on the basis of cross-resistance to beta-aspartyl hydroxamate, another amino acid analog. Studies on asparagine synthetase indicate that resistance to albizziin may be due to altered regulation of asparagin
价 格：￥电议型 号：T69056产 地：中国大陆
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T6895TAK-580；化合物MLN2480MLN2480|||BIIB-024；MLN2480|||BIIB-024
TAK-580 (MLN2480) is an oral, selective pan-Raf kinase inhibitor in Clinicalal trials.
价 格：￥电议型 号：T6895产 地：中国大陆
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T68383BIIB028；化合物 BIIB028BIIB028
BIIB028 is a small-molecule inhibitor of heat shock protein (Hsp) 90 with potential antineoplastic activity. Hsp90 inhibitor BIIB028 blocks the binding of oncogenic client proteins to Hsp90, which may result in the proteasomal degradation of these proteins and so the inhibition of tumor cell proliferation. Hsp90 is a molecular chaperone that plays a key role in the conformational maturation of oncogenic signaling proteins, such as Her2/Erbb2, Akt, Raf1, Bcr-Abl, and mutated p53, in addition to o
价 格：￥电议型 号：T68383产 地：中国大陆
