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T80344Aeschna defensin；化合物 Aeschna defensinAeschna defensin
Aeschna defensin is an antimicrobial peptide sourced from the hemolymph of aquatic dragonfly larvae, exhibiting potent activity against Gram-positive bacteria [1].
价 格：￥电议型 号：T80344产 地：中国大陆
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T79955Schiarisanrin A；化合物 Schiarisanrin AKadsulignan J；Kadsulignan J
Schiarisanrin A (Kadsulignan J), a lignan, exhibits inhibitory activity on nitric oxide (NO) production, demonstrating an IC50 of 9.6 μM in BV-2 cells [1].
价 格：￥电议型 号：T79955产 地：中国大陆
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T76784Tildrakizumab；替瑞奇珠单抗MK 3222|||SCH 900222；MK 3222|||SCH 900222
Tildrakizumab (SCH 900222) is a potent humanized monoclonal antibody against IL-23 (p19 subunit). Tildrakizumab targets single-stranded IL-23 with a Kd value of 136 pM. Tildrakizumab can be used to study psoriasis and psoriasis.
价 格：￥电议型 号：T76784产 地：中国大陆
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T76711Golimumab；戈利木单抗MK-8259|||SCH 900259|||CNTO-148；MK-8259|||SCH 900259|||CNTO-148
Golimumab (CNTO-148) is a potent humanized anti-TNFα IgG1κ monoclonal antibody.Golimumab has anti-inflammatory and anticancer activity, inhibits the production of IL-6 and IL-1β, and induces apoptosis.Golimumab can be used to prevent inflammation and destruction of cartilage or bone, and can be used to study rheumatoid arthritis and cancer. Golimumab can be used to prevent inflammation and cartilage or bone destruction and can be used to study rheumatoid arthritis and cancer.
价 格：￥电议型 号：T76711产 地：中国大陆
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T76111Hexokinase (ScHEX1)；化合物 Hexokinase (ScHEX1)Hexokinase (ScHEX1)
Hexokinase (ScHEX1), a glycolytic enzyme, is inhibited by n-acetylglucosamine, which causes it to detach from the mitochondrial outer membrane. This detachment activates the NLRP3 inflammasome [1].
价 格：￥电议型 号：T76111产 地：中国大陆
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T7549619-epi-Scholaricine；化合物 19-epi-Scholaricine19-epi-Scholaricine
19-epi-Scholaricine, an orally active indole alkaloid, downregulates collagen fibrosis expression and enhances superoxide dismutase (SOD) activities.
价 格：￥电议型 号：T75496产 地：中国大陆
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T75476Monaschromone；化合物 MonaschromoneMonaschromone
Monaschromone, a polyketide metabolite, effectively suppresses the growth of B. cinerea, A. solani, M. oryzae, and G. saubinettii, demonstrating minimum inhibitory concentration (MIC) values between 6.25 and 12.5 μM [1].
价 格：￥电议型 号：T75476产 地：中国大陆
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T73981Deschloro Cetirizine dihydrochloride；化合物 Deschloro Cetirizine dihydrochlorideDeschloro Cetirizine di
Deschloro Cetirizine Dihydrochloride is an impurity of Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine. It functions as a specific, orally active, and long-acting histamine H1-receptor antagonist.
价 格：￥电议型 号：T73981产 地：中国大陆
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T72733Geissoschizoline；化合物 Geissoschizoline(+)-Geissoschizoline；(+)-Geissoschizoline
Geissoschizoline ((+)-Geissoschizoline), with IC50 values of 20.40 ?M for human AChE and 10.21 ?M for BChE, functions as a potent inhibitor and emerges as a promising multi-target prototype for research into preventing neurodegeneration and restoring neurotransmission. Additionally, it serves as a potent anti-inflammatory agent.
价 格：￥电议型 号：T72733产 地：中国大陆
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T72707(Rac)-Lonafarnib；化合物 (Rac)-LonafarnibSch66336 racemate；Sch66336 racemate
(Rac)-Lonafarnib (Sch66336 racemate) is the racemic form of the potent, orally active farnesyl transferase (FTase) inhibitor, Lonafarnib. It effectively inhibits H-ras, K-ras, and N-ras with IC50 values of 1.9 nM, 5.2 nM, and 2.8 nM, respectively. Additionally, Lonafarnib exhibits activities against the hepatitis delta virus (HDV).
价 格：￥电议型 号：T72707产 地：中国大陆
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T7130Navarixin；化合物NavarixinMK-7123|||SCH 527123；MK-7123|||SCH 527123
Navarixin (MK-7123)(SCH527123) is a novel, selective CXC chemokine receptor 2(CXCR2) antagonist that inhibits neutrophil activation and modulates neutrophil trafficking in animal models, characteristics that may be beneficial in the treatment of conditions with unbalanced pulmonary neutrophilia.
价 格：￥电议型 号：T7130产 地：中国大陆
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T71201SCH-900822；化合物 SCH-900822SCH-900822
SCH-900822 is a potent and selective glucagon receptor antagonist.
价 格：￥电议型 号：T71201产 地：中国大陆
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T7013Vorapaxar；沃拉帕沙SCH 530348|||MK-5348；SCH 530348|||MK-5348|||沃拉帕沙
Vorapaxar (MK-5348) (SCH 530348) is an effective and orally active thrombin receptor (PAR-1) antagonist (Ki: 8.1 nM).
价 格：￥电议型 号：T7013产 地：中国大陆
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T70056Moschamine；化合物 MoschamineMoschamine
Moschamine is an inhibitor of mitochondrial superoxide overproduction.
价 格：￥电议型 号：T70056产 地：中国大陆
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T70048Sch 58053；化合物 Sch 58053Sch 58053
Sch 58053 is an analog of Ezetimibe and a selective inhibitor of lymphatic cholesterol transport in the intestine.
价 格：￥电议型 号：T70048产 地：中国大陆
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T6S1930Schisanhenol；五味子酚Schizanhenol|||Gomisin-K3；五味子酚|||Schizanhenol|||Gomisin-K3
1. Schisanhenol (Schizanhenol) can protect against adriamycin induced heart mitochondrial toxicity. 2. Schisanhenol has antioxidative effect on human LDL oxidation, may be through scavenging free radicals. 3. Schisanhenol has anti-apoptosis effect on BACSs, may be related to its inhibition of ROS generation.
价 格：￥电议型 号：T6S1930产 地：中国大陆
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T6S1918Schisantherin B；五味子酯乙Gomisin-B|||Wuweizi ester-B|||Schizantherin-B；Gomisin-B|||Wuweizi ester-B|||五味子
1. Schisantherin B (Schizantherin-B) shows good effect in lowering the serum glutamic-pyruvic transaminase level of the patients suffering from chronic virus hepatitis.
价 格：￥电议型 号：T6S1918产 地：中国大陆
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T6S1917Schisandrol B；五味子醇乙Gomisin A|||TJN-101|||Besigomsin|||Gamma-Schisandrin|||Schizandrol B|||Wuweizi al
1. Schisandrol B (Besigomsin) may exert neuroprotective effects by attenuating the microglia-mediated neuroinflammatory response via inhibiting the TLR4-mediated NF-κB and MAPKs signaling pathways. 2. Schisandrol B has anti-inflammatory property, potentially result from the inhibition of COX-2, iNOS, IL-6, TNF-α and NO through the down-regulation of RIP2 and NF-κB activation. 3. Schisandrol B induces marked protective effects against hepatic and renal injury induced by CCl(4) exposure through di
价 格：￥电议型 号：T6S1917产 地：中国大陆
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T6979SCH 58261；化合物SCH58261SCH58261；SCH58261
SCH 58261 is a potent and selective A2a adenosine receptor antagonist.The Ki =2.3 nM for rat A2a and 2 nM is for bovine A2a.
价 格：￥电议型 号：T6979产 地：中国大陆
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T69737SCH-79687；化合物 SCH-79687SCH-79687
SCH-79687 is a histamine antagonist selective for the H3 subtype. This H3 antagonist may play a role in allergic rhinitis.
价 格：￥电议型 号：T69737产 地：中国大陆
