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T24592Pamaqueside;化合物 T24592CP-148,623|||CP 148623|||L 165313|||L165313|||L-165313;CP-148,623|||CP 148623|
Pamaqueside is an anti-atherosclerotic agent.
价 格:¥电议型 号:T24592产 地:中国大陆
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T24550NSC-140873;化合物 T24550GCPK;GCPK
NSC-140873 is the RUNX1-CBFβ interaction inhibitor.
价 格:¥电议型 号:T24550产 地:中国大陆
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T24465Milacemide HCl;化合物 T24465Milacemide Hydrochloride salt|||SC-45864|||Milacemide HCl salt|||CP-1552S||
Milacemide HCl is an MAO-B inhibitor and glycine prodrug.
价 格:¥电议型 号:T24465产 地:中国大陆
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T24437MCP110;化合物MCP110MCP-110|||MCP 110;MCP-110|||MCP 110
MCP110 is an inhibitor of the interaction of Ras with Raf-1 and can be used in studies about the treatment of human tumors.
价 格:¥电议型 号:T24437产 地:中国大陆
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T2442CPI203;化合物CPI-203CPI 203|||CPI-203;CPI 203|||CPI-203
CPI203 (CPI 203) is an effective BET bromodomain inhibitor (IC50: 37 nM for BRD4).
价 格:¥电议型 号:T2442产 地:中国大陆
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T24146HOCPCA;化合物 T24146HOCPCA
HOCPCA is an effective and selective ligand for the GHB binding sites that acts by binding with 27 times better affinity than GHB itself and crossing the blood-brain barrier in vitro and in vivo.
价 格:¥电议型 号:T24146产 地:中国大陆
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T24051Exisulind;化合物ExisulindSulindac sulfone|||CP248;Sulindac sulfone|||CP248
Exisulind (CP248) induces apoptosis through the activation of protein kinase G (PKG). Exisulind exhibits antineoplastic activity in solid tumour and haematological cancer cell lines and is an inhibitor of tumour growth in rodent models of colon, prostate, bladder, mammary and lung cancer.
价 格:¥电议型 号:T24051产 地:中国大陆
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T2398Tofacitinib Citrate;枸橼酸托法替尼CP-690550 citrate|||Tasocitinib citrate|||Tofacitinib (CP-690550) Citrate
Tofacitinib Citrate (CP-690550 citrate) is a a potent, cell-permeable inhibitor of JAK1/2/3 (IC50s: 1/20/112 nM).
价 格:¥电议型 号:T2398产 地:中国大陆
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T23912CPSA;化合物 T23912CPSA
CPSA is an effective and selective AKR1C1 inhibitor.
价 格:¥电议型 号:T23912产 地:中国大陆
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T23911CPS-11;化合物CPS-11CPS11|||CPS 11|||N-(Hydroxymethyl)thalidomide;CPS11|||CPS 11|||N-(Hydroxymethyl)thal
CPS-11 (N-(Hydroxymethyl)thalidomide) is a Thalidomide analogue that has significant antitumor activity and exhibits a wider range of activity and highly potent effects on the MM (multiple myeloma) cell line.
价 格:¥电议型 号:T23911产 地:中国大陆
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T23864CCPG;化合物 T23864(alpha-Carboxycyclopropyl)glycine|||L-Ccg-I;(alpha-Carboxycyclopropyl)glycine|||L-Ccg
CCPG is an agonist of excitatory Amino Acid.
价 格:¥电议型 号:T23864产 地:中国大陆
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T23738Anthglutin;化合物 T23738GGCPH;GGCPH
Anthglutin is a reversible glutamyl transpeptidase inhibitor.
价 格:¥电议型 号:T23738产 地:中国大陆
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T23686AHR-activator-1023;化合物 T23686Branching Morphogenesis Modulator 1023|||Cpd 1023|||Compound 1023|||BMM
AHR-activator-1023 is the aryl hydrocarbon receptor activator. It is also a specific FGF2-induced branching morphogenesis modulator.
价 格:¥电议型 号:T23686产 地:中国大陆
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T235889-CP-Ade Mesylate;9-CP-Ade甲磺酸盐9-Cyclopentyladenine monomethanesulfonate|||9 CP Ade Mesylate|||9CPAde
9-CP-Ade Mesylate (9 CP Ade Mesylate) is a cell-permeable, stable and non-competitive inhibitor of adenylate cyclase.
价 格:¥电议型 号:T23588产 地:中国大陆
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T23554(Z)-FeCP-oxindole;化合物(Z)-FeCP-oxindole(Z)-FeCP-oxindole
(Z)-FeCP-oxindole is a selective inhibitor of VEGFR2 with an IC50 of 200 nM for human. (Z)-FeCP-oxindole shows anticancer activity.
价 格:¥电议型 号:T23554产 地:中国大陆
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T23288L(S)-3,4-DCPG HCl;(S)-3,4-DCPG 盐酸盐(S)-3,4-Dicarboxyphenylglycine HCl|||(S)-3,4-DCPG HCl(201730-11-2 F
(S)-3,4-DCPG HCl ((S)-3,4-Dicarboxyphenylglycine HCl) is a selective metabotropic glutamate receptor 8a (mGluR8a) agonist that has an effect on human mGluR8-expressing AV12-664 cells with an EC50 of 31 nM.
价 格:¥电议型 号:T23288L产 地:中国大陆
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T23288(S)-3,4-DCPG;化合物(S)-3,4-DCPG(S)-3,4-Dicarboxyphenylglycine;(S)-3,4-Dicarboxyphenylglycine
(S)-3,4-DCPG ((S)-3,4-Dicarboxyphenylglycine) is a selective agonist of human metabotropic glutamate receptor 8a (mGluR8a).
价 格:¥电议型 号:T23288产 地:中国大陆
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T23270(RS)-MCPG disodium salt;化合物 T23270(RS)-MCPG disodium salt
group I/group II metabotropic glutamate receptor antagonist
价 格:¥电议型 号:T23270产 地:中国大陆
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T23257(RS)-3,4-DCPG;化合物 T23257(RS)-3,4-DCPG
antagonist of AMPA receptors and agonist of mGluR8
价 格:¥电议型 号:T23257产 地:中国大陆