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T81027TCRS-417；化合物 TCRS-417T417；T417
TCRS-417 (T417), a small molecule compound, selectively binds to the interface between PBX1 and its specific DNA target sequence, disrupting the PBX1-DNA interaction. This compound has potential research applications in cancer, developmental, inflammatory, autoimmune, and neurodegenerative diseases [1].
价 格：￥电议型 号：T81027产 地：中国大陆
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T71027KDI-792 hydrochloride；化合物 KDI-792 hydrochlorideKDI-792 hydrochloride
KDI-792 hydrochloride is a thromboxane dual blocker.
价 格：￥电议型 号：T71027产 地：中国大陆
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T6S1027Tussilagone；款冬酮Tussilagone
1. Tussilagone inhibits dendritic cell function through the induction of heme oxygenase-1. 2. Tussilagone has anti-cancer activity, might be a potential chemotherapeutic agent for the prevention and treatment of human colon cancer. 3. Tussilagone has anti-oxidant and anti-inflammatory activities, may be an effective oxygenase-1 inducer and a valuable compound for modulating inflammatory conditions. 4. Tussilagone has potential treatment of neuro-inflammatory diseases through the inhibition of ov
价 格：￥电议型 号：T6S1027产 地：中国大陆
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T6135YO-01027二苯并氮卓gamma-Secretase Inhibitor XX|||Dibenzazepine|||DBZ|||二苯并氮卓
YO-01027 (DBZ) is a potent γ-secretase inhibitor.
价 格：￥电议型 号：T6135产 地：中国大陆
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T61027Piribedil hydrochloride；化合物 Piribedil hydrochloridePiribedil hydrochloride
Piribedil hydrochloride can be used in the parkinson´s disease, circulatory disorders, cancers research. Piribedil hydrochloride inhibits MLL1 methyltransferase activity with EC50 value of 0.18 μM. Piribedil hydrochloride is a potent and orally active agonist of dopamine D2 and dopamine D3 as well as the antagonist of α2-adrenoceptors [1] [2] [3] [4].
价 格：￥电议型 号：T61027产 地：中国大陆
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T41027MLKL-IN-2；MLKL抑制剂2MLKL-IN-2
MLKL-IN-2 is an MLKL inhibitor with potential tumorigenic activity for the study of cellular necrosis-related diseases.
价 格：￥电议型 号：T41027产 地：中国大陆
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T35150X 910279；化合物 T35150MNA-279|||X91 0279|||HMR 279|||HMR 1279|||MNA 279；MNA-279|||X91 0279|||HMR 279|||
X 910279 is a leflunomide analog and a malononitrilamide.
价 格：￥电议型 号：T35150产 地：中国大陆
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T31027CP-67015；化合物 T31027CP-67,015|||CCRIS 2955；CP-67,015|||CCRIS 2955
CP 67015 has an inhibitory effect on the function of topoisomerase, and is a direct mutagen in mammalian cells, which has effects on gene and chromosome levels.
价 格：￥电议型 号：T31027产 地：中国大陆
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T30279Azotomycin sodium；化合物 T30279Antibiotic 1719 sodium salt|||A 10270B|||A10270B|||A-10270B|||1719 Sodiu
Azotomycin sodium is the sodium salt of Azotomycin.
价 格：￥电议型 号：T30279产 地：中国大陆
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T24421LY-2624803；化合物LY-2624803DB-7|||LY2624803|||HY-10275|||LY 2624803；DB-7|||LY2624803|||HY-10275|||LY 26
LY-2624803 is a 5-HT2A receptor antagonist and histamine receptor inverse agonist that can be used to improve slow wave sleep.
价 格：￥电议型 号：T24421产 地：中国大陆
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T21027Guar gum；化合物 T21027Guaran|||Gum cyamopsis|||Gum guar|||Guar flour；Guaran|||Gum cyamopsis|||Gum guar|
Guar gum is a galactomannan polysaccharide extracted from guar beans, it has stabilizing and thickening properties useful in food, feed, and industrial applications.
价 格：￥电议型 号：T21027产 地：中国大陆
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T1904SGI-1027；化合物SGI-1027DNA Methyltransferase Inhibitor II|||SGI1027；DNA Methyltransferase Inhibitor II|
SGI-1027 (DNA Methyltransferase Inhibitor II) is an effective and selective inhibitor of DNA methyltransferase (DNMT). The IC50 of SGI-1027(SGI1027) against DNMT1, DNMT3A, and DNMT3B are 6, 8, 7.5 μM, respectively.
价 格：￥电议型 号：T1904产 地：中国大陆
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T1813VGX-1027；化合物VGX-1027VGX1027|||VGX 1027|||GIT 27；VGX1027|||VGX 1027|||GIT 27
VGX-1027 (GIT 27) is an isoxazole compound with various immunomodulatory properties.
价 格：￥电议型 号：T1813产 地：中国大陆
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T15015CTS-1027；化合物 T15015RS 130830|||Ro 1130830；RS 130830|||Ro 1130830
CTS-1027 is a small molecule inhibitor of MMPs (IC50s: 0.3 nM, 0.5 nM for MMP2, MMP13). It has > 1,000 fold selectivity over MMP1.
价 格：￥电议型 号：T15015产 地：中国大陆
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T14350Soblidotin；化合物SoblidotinAuristatin PE|||TZT-1027；Auristatin PE|||TZT-1027
Soblidotin (TZT-1027) (Auristatin PE) is an inhibitor of tubulin polymerization. It is also a novel synthetic Dolastatin 10 derivative.
价 格：￥电议型 号：T14350产 地：中国大陆
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T11027DHODH-IN-4；化合物DHODH-IN-4DHODH-IN-4
DHODH-IN-4 is a human and Plasmodium falciparum dihydroorotate dehydrogenase (DHODH) inhibitor. The IC50 values of PfDHODH and HsDHODH are 4 μM and 0.18 μM, respectively. DHODH-IN-4 has antimalarial activity.
价 格：￥电议型 号：T11027产 地：中国大陆
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T10279Alfacalcidol-D6；化合物 T10279Alfacalcidol-D6
Alfacalcidol-D6 is a deuterated Alfacalcidol. Alfacalcidol is a non-selective VDR activator medication.
价 格：￥电议型 号：T10279产 地：中国大陆
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T10278Alamethicin；丙甲菌素Alamethicin
Alamethicin is isolated from Trichoderma viride. It is a channel-forming peptide antibiotic and induces voltage-gated conductance in model and cell membranes.
价 格：￥电议型 号：T10278产 地：中国大陆
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T10277AL 8697；化合物AL 8697AL 8697
AL 8697 is a selective p38α MAPK inhibitor (IC50 = 6 nM) with 14-fold selectivity over p38β (IC50 = 82 nM) and 300-fold selectivity over a panel of 91 kinases. AL 8697 has anti-inflammatory activity.
价 格：￥电议型 号：T10277产 地：中国大陆
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T10276LAKT Kinase Inhibitor HCl；AKT Kinase抑制剂盐酸盐AKT Kinase Inhibitor HCl(842148-40-7 Free base)；AKT Kinase
AKT Kinase Inhibitor HCl is an Akt inhibitor with antitumor activity.
价 格：￥电议型 号：T10276L产 地：中国大陆
