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产品数：86101
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T86022-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1LAMBDA*6*-BENZO[D]ISOTHIAZOL-3-ONE；化合物T86022-CHLOROMETHYL-1,1-
2-CHLOROMETHYL-1,1-DIOXO-1,2-DIHYDRO-1LAMBDA*6*-BENZO[D]ISOTHIAZOL-3-ONE targets the Neutrophil elastase (human).
价 格：￥电议型 号：T8602产 地：中国大陆
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T86011-benzyl-2-ethyl-4,5,6,7-tetrahydro-1H-indol-4-one；化合物T86014H-Indol-4-one, 2-ethyl-1,5,6,7-tetrahydr
1-benzyl-2-ethyl-4,5,6,7-tetrahydro-1H-indol-4-one is an inhibitor Bromodomain-containing protein 4 (human).
价 格：￥电议型 号：T8601产 地：中国大陆
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T8600N-ACETYLTRYPTAMINE；N-乙酰基色胺N-ACETYLTRYPTAMINE
N-ACETYLTRYPTAMINE is a partial agonist for melatonin receptors in the retina. Also used for determination of serotonin N-acetyl transferase.
价 格：￥电议型 号：T8600产 地：中国大陆
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T83860ABD-F；化合物 ABD-FABD-F
ABD-F, a thiol-reactive fluorogenic reagent, is employed for the detection and quantification of thiol-containing amino acids, protein and tissue thiols, as well as disulfide bridges between proteins. It exhibits excitation/emission maxima at 389 nm and 513 nm, respectively.
价 格：￥电议型 号：T83860产 地：中国大陆
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T82860Bis[3,4,6-trichloro-2-(pentyloxycarbonyl)phenyl] oxalate；化合物 Bis[3,4,6-trichloro-2-(pentyloxycarbony
Bis[3,4,6-trichloro-2-(pentyloxycarbonyl)phenyl] oxalate is a fluorescent dye capable of chemiluminescence generation [1].
价 格：￥电议型 号：T82860产 地：中国大陆
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T81860MARK4 inhibitor 4；化合物 MARK4 inhibitor 4MARK4 inhibitor 4
MARK4 inhibitor 4, with an IC50 value of 1.49 μM, serves as an agent targeting MARK4 for potential use in research related to cancer and tauopathies [1].
价 格：￥电议型 号：T81860产 地：中国大陆
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T80860Vitisin B；化合物 Vitisin B(-)-Vitisin B|||E-Vitisin B；(-)-Vitisin B|||E-Vitisin B
Vitisin B (Compound 5), isolated from Vitis thunbergii var. taiwaniana, exhibits anti-inflammatory properties in cases of lipopolysaccharide (LPS)-induced arthritis [1].
价 格：￥电议型 号：T80860产 地：中国大陆
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T79908ON 108600；化合物 ON 108600ON 108600
ON 108600 is a chemical inhibitor targeting CK2 (Casein Kinase 2), TNIK, and DYRK1, demonstrating IC50 values of 0.016 μM and 0.007 μM for DYRK1A and DYRK1B, 0.028 μM for DYRK2, 0.05 μM and 0.005 μM for CK2α1 and CK2α2, and 0.005 μM for TNIK, respectively. This compound exhibits antitumor activity [1].
价 格：￥电议型 号：T79908产 地：中国大陆
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T79860TIE-2/VEGFR-2 kinase-IN-5；TIE-2/VEGFR-2 kinase 抑制剂5TIE-2/VEGFR-2 kinase-IN-5
TIE-2/VEGFR-2 kinase-IN-5 is a potent TIE-2 and VEGFR-2 tyrosine kinase receptor inhibitor with anti-angiogenic activity and is commonly used in biomedical research related to angiogenesis.
价 格：￥电议型 号：T79860产 地：中国大陆
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T79264Z1078601926；化合物 Z1078601926Z1078601926
Z1078601926 is an allosteric inhibitor of the human dopamine transporter (hDAT) and exhibits a synergistic effect when combined with Nomifensine [1].
价 格：￥电议型 号：T79264产 地：中国大陆
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T78860MAO-B-IN-24；化合物 MAO-B-IN-24MAO-B-IN-24
MAO-B-IN-24 (compound 11h) is a selective, reversible, competitive inhibitor of MAO-B with an IC50 value of 1.60 μM. It also exhibits inhibitory effects on MAO-A with an IC50 of 22.42 μM. At a concentration of 10 μM, MAO-B-IN-24 reduces the activities of AChE and BChE to 54.58% and 88.43%, respectively [1].
价 格：￥电议型 号：T78860产 地：中国大陆
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T78608Anticancer agent 164；化合物 Anticancer agent 164Anticancer agent 164
CML-IN-1, also known as compound 7 and compound 4, is a potent anticancer agent that demonstrates a strong induced-apoptosis effect in the human chronic myeloid leukemia (CML) cell line K562. It diminishes protein phosphorylation within the PI3K/Akt signaling pathway to exert its effects and suppresses cell proliferation through the inhibition of the MEK/ERK signaling pathway in colorectal cancer [1] [2].
价 格：￥电议型 号：T78608产 地：中国大陆
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T78607JAK-STAT-IN-1；JAK-STA 抑制剂1JAK-STAT-IN-1
JAK-STAT-IN-1 is a specific JAK-STAT inhibitor indicated for the study of autoimmune diseases.
价 格：￥电议型 号：T78607产 地：中国大陆
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T78606P2X3-IN-1；化合物 P2X3-IN-1P2X3-IN-1
P2X3-IN-1 (example 7) is a P2X3 receptor inhibitor suitable for research on neurogenic diseases [1].
价 格：￥电议型 号：T78606产 地：中国大陆
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T78605CpCDPK1/TgCDPK1-IN-1；CpCDPK1/TgCDPK1抑制剂1CpCDPK1/TgCDPK1-IN-1
CpCDPK1/TgCDPK1-IN-1 is a potent dual inhibitor of CpCDPK1 and TgCDPK1, inhibits Abl and Src, and has antiparasitic activity for the study of Toxoplasma infections and cryptosporidiosis.
价 格：￥电议型 号：T78605产 地：中国大陆
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T78604SLC26A3-IN-3；化合物 SLC26A3-IN-3SLC26A3-IN-3
SLC26A3-IN-3 (compound 4az), a potent SLC26A3 inhibitor with an IC50 of 40 nM, is utilized for constipation and cystic fibrosis research [1].
价 格：￥电议型 号：T78604产 地：中国大陆
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T78603Sotuletinib dihydrochloride；化合物 Sotuletinib dihydrochlorideBLZ945 dihydrochloride；BLZ945 dihydrochlo
Sotuletinib (BLZ945) dihydrochloride is an orally administered, blood-brain barrier-permeable inhibitor specifically targeting CSF1-R with an IC50 of 1 nM. It promotes apoptosis in tumor cells and significantly restricts tumor growth in murine models, proving useful in cancer and amyotrophic lateral sclerosis (ALS) studies [1].
价 格：￥电议型 号：T78603产 地：中国大陆
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T78602Chaetoglobosin C；化合物 Chaetoglobosin CChaetoglobosin C
Chaetoglobosin C (Compound 4), an anthraquinone-chromone derivative of Chaetomium globosum KMITL-N0802, exhibits anti-tuberculosis activity [1].
价 格：￥电议型 号：T78602产 地：中国大陆
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T78600VU0029251；化合物 VU0029251VU0029251
VU0029251 serves as a partial antagonist of mGluR5, exhibiting a binding affinity with a K i of 1.07 μM. It also attenuates glutamate-induced calcium mobilization in HEK293 cell membranes that express rat mGluR5, demonstrating an IC 50 of 1.7 μM [1].
价 格：￥电议型 号：T78600产 地：中国大陆
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T7860SM-324405；化合物SM 324405SM 324405；SM 324405
SM-324405 is an agonist of TLR7.
价 格：￥电议型 号：T7860产 地：中国大陆
