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T81930Linderanine C；化合物 Linderanine C(-)-Linderanine C；(-)-Linderanine C
Linderanine C ((-)-Linderanine C) (compound 6), a sesquiterpenoid, can be extracted from the roots of Wuyao [1].
价 格：￥电议型 号：T81930产 地：中国大陆
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T8193α-Thujone；α-侧柏酮Thujone|||ALPHA-(-)-THUJONE；Thujone|||ALPHA-(-)-THUJONE|||α-侧柏酮|||(-)-α-侧柏酮
α-Thujone is an inhibitor of ACh with an IC50 value of 24.7μM.
价 格：￥电议型 号：T8193产 地：中国大陆
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T81193Schineolignin C；化合物 Schineolignin CSchineolignin C
Schisandrin C, a lignan extracted from the fruit of Schisandra chinensis, exhibits antihepatitis, antitumor, and anti-HIV-1 activities [1].
价 格：￥电议型 号：T81193产 地：中国大陆
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T80193Enterocin Hybrid 1；化合物 Enterocin Hybrid 1K1-EJ hybrid；K1-EJ hybrid
Enterocin Hybrid 1, an antibacterial agent, effectively inhibits Vancomycin-resistant Enterococcus faecium and Staphylococcus haemolyticus [1].
价 格：￥电议型 号：T80193产 地：中国大陆
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T79193DRI-C21041；化合物 DRI-C21041DRI-C21041
DRI-C21041 is a potent inhibitor of the CD40/CD40L interaction, demonstrating an inhibitory concentration 50 (IC50) value of 0.31 μM. It effectively suppresses the immune response triggered by alloantigen [1].
价 格：￥电议型 号：T79193产 地：中国大陆
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T78402’,3’,5’-triacetyl-5-Azacytidine；三乙酰基-阿扎胞苷Nsc291930；Nsc291930|||三乙酰基-阿扎胞苷
2´,3´,5´-triacetyl-5-Azacytidine (Nsc291930) is a prodrug form of 5-azacytidine that may be rapidly absorbed orally.
价 格：￥电议型 号：T7840产 地：中国大陆
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T78092UCL-TRO-1938；化合物 UCL-TRO-1938UCL-TRO-1938
UCL-TRO-1938, a potent allosteric activator of PI3Kα, exhibits an EC50 of approximately 60 μM. This compound promotes cell proliferation and possesses both cardioprotective and neural regeneration effects [1].
价 格：￥电议型 号：T78092产 地：中国大陆
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T76193PINT-87aa；化合物 PINT-87aaPINT-87aa
PINT-87aa, an 87-amino acid (aa) peptide encoded by the circular form of the long intergenic non-protein-coding RNA p53-induced transcript (LINC-PINT), directly interacts with the polymerase associated factor complex (PAF1c) to inhibit the transcriptional elongation of multiple oncogenes. This interaction effectively suppresses glioblastoma cell proliferation both in vitro and in vivo [1].
价 格：￥电议型 号：T76193产 地：中国大陆
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T751933’-Beta-C-Ethynyl-4-deoxyuridine；化合物 3’-Beta-C-Ethynyl-4-deoxyuridine3’-Beta-C-Ethynyl-4-deoxyuridin
3’-Beta-C-Ethynyl-4-deoxyuridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis , etc [1] .
价 格：￥电议型 号：T75193产 地：中国大陆
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T74193(R)-IDHP；化合物 (R)-IDHP(R)-IDHP
(R)-IDHP, an isomer of IDHP and a metabolite of salvia, exhibits vasorelaxant properties by inhibiting calcium (Ca 2+) release and inward flow through both voltage-dependent and receptor-operated calcium channels in vascular smooth muscle cells. It is utilized in cardiovascular disease research [1].
价 格：￥电议型 号：T74193产 地：中国大陆
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T73225OTS193320；化合物 OTS193320OTS193320
OTS193320, an imidazopyridine compound, acts as an inhibitor of SUV39H2 methyltransferase activity. It effectively reduces global histone H3 lysine 9 tri-methylation levels in breast cancer cells, promoting apoptotic cell death. When combined with Doxorubicin (DOX; HY-15142A), OTS193320 enhances the reduction of γ-H2AX levels and decreases cancer cell viability more significantly than when either agent is used alone.
价 格：￥电议型 号：T73225产 地：中国大陆
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T72193Octenyl succinic anhydride；化合物 Octenyl succinic anhydrideOctenyl succinic anhydride
Octenyl succinic anhydride (OSA) is utilized to esterify starch, producing octenyl succinylated starch (OS-starch), a hydrocolloid with amphiphilic properties. This modification by OSA influences the interaction between molecules on the outer surface of starch granules through alterations in molecular structures.
价 格：￥电议型 号：T72193产 地：中国大陆
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T71939PS77；化合物 PS77PS77|||PS-77|||SLR080811|||PS 77|||SLR 080811.；PS77|||PS-77|||SLR080811|||PS 77|||SLR 0
PS77 is a Pkh inhibitor directed to the PIF-pocket with increased selectivity for C. albicans Pkh2.
价 格：￥电议型 号：T71939产 地：中国大陆
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T71938MNF；化合物 MNFMNF
MNF, also known as 3,4-MNF, is an antagonist of the aryl hydrocarbon receptor (AhR). MNF reduces UVR-mediated immunosuppression and induces Tregs in murine contact hypersensitivity (CHS).
价 格：￥电议型 号：T71938产 地：中国大陆
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T71937Nitrodenafil；化合物 NitrodenafilNitrodenafil
Nitrodenafil is a related compound of Sildenafil -- a phosphodiesterase inhibitor.
价 格：￥电议型 号：T71937产 地：中国大陆
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T71936Phenylthiazolylthiourea；化合物 PhenylthiazolylthioureaPhenylthiazolylthiourea
Phenylthiazolylthiourea ia a dopamine-beta-hydroxylase inhibitor.
价 格：￥电议型 号：T71936产 地：中国大陆
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T71935WIN 66306；化合物 WIN 66306WIN 66306
WIN 66306 is a cyclic heptapeptide antagonist of neurokinin-1 (NK1) and NK2 receptors originally isolated from A. flavipes. It binds to NK1 and NK2 receptors and inhibits contractions induced by substance P in isolated guinea pig ileum in a concentration-dependent manner.
价 格：￥电议型 号：T71935产 地：中国大陆
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T71934Atibeprone；阿替普隆Atibeprone
Atibeprone is a MAO-B inhibitor with antidepressant activity for the study of Parkinson´s disease.
价 格：￥电议型 号：T71934产 地：中国大陆
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T71933GNE-3500；化合物 GNE-3500GNE-3500
GNE-3500 is a Potent, Selective, and Orally Bioavailable Retinoic Acid Receptor-Related Orphan Receptor C (RORc or RORγ) Inverse Agonist. Retinoic acid receptor-related orphan receptor C (RORc, RORγ, or NR1F3) is a nuclear receptor that plays a major role in the production of interleukin (IL)-17. Considerable efforts have been directed toward the discovery of selective RORc inverse agonists as potential treatments of inflammatory diseases such as psoriasis and rheumatoid arthritis. GNE-3500 poss
价 格：￥电议型 号：T71933产 地：中国大陆
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T71931Clencyclohexerol；化合物 ClencyclohexerolClencyclohexerol
Clencyclohexerol is an analog of clenbuterol. β-Adrenoceptor agonists, including clenbuterol, modulate protein synthesis and degradation and have therapeutic potential in muscle wasting disorders. β-adrenoceptor agonists have deleterious cardiovascular side effects when used systemically and at high concentrations.
价 格：￥电议型 号：T71931产 地：中国大陆
