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T2603Spebrutinib；化合物SpebrutinibCC-292|||LMK-435|||AVL-292；CC-292|||LMK-435|||AVL-292
Spebrutinib (LMK-435) is an orally bioavailable, selective inhibitor of Bruton´s agammaglobulinemia tyrosine kinase (BTK), with potential antineoplastic activity.
价 格：￥电议型 号：T2603产 地：中国大陆
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T25594Laccaic acid A；化合物 T25594Laccaic acid A
Laccaic acid A is a direct, DNA-competitive DNA methyltransferase 1 inhibitor.
价 格：￥电议型 号：T25594产 地：中国大陆
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T25551Jmv 236；化合物 T25551Jmv236|||t-Boc(nle(28,31))-cck (26-33)|||Jmv-236；Jmv236|||t-Boc(nle(28,31))-cck (2
Jmv 236 is a cholecystokinin antagonist.
价 格：￥电议型 号：T25551产 地：中国大陆
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T2552Succimer二巯基丁二酸DMSA|||Dimercaptosuccinic acid|||二巯基丁二酸|||meso-2,3-dimercaptosuccinic acid|||内消旋-2,3-二
Succimer (Dimercaptosuccinic acid) is a Lead Chelator. The mechanism of action of succimer is as a Lead Chelating Activity.
价 格：￥电议型 号：T2552产 地：中国大陆
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T25318DHPCC-9；化合物 T25318DHPCC9；DHPCC9
DHPCC-9 is an inhibitor of Pim kinase.
价 格：￥电议型 号：T25318产 地：中国大陆
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T25292DCCCyb；化合物 T25292DCCCyb
DCCCyb is an orally bioavailable and selective GlyT1 Inhibitor. DCCCyb demonstrated excellent in vivo occupancy of GlyT1 transporters in rhesus monkeys as determined by the displacement of a PET tracer ligand.
价 格：￥电议型 号：T25292产 地：中国大陆
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T25240Chloramphenicol succinate；化合物 T25240Paraxin succinate|||Kemicetine succinate|||CPSA；Paraxin succinat
Chloramphenicol succinate is an inactive precursor of chloramphenicol. It is used for parenteral administration of chloramphenicol.
价 格：￥电议型 号：T25240产 地：中国大陆
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T25215CCT077791；化合物CCT077791CCT 077791|||CCT-077791；CCT 077791|||CCT-077791
CCT077791 is a potent inhibitor of p300 and PCAF histone acetyltransferase activity for cancer research.
价 格：￥电议型 号：T25215产 地：中国大陆
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T25214CCR-11；化合物 CCR-11CCR11|||CCR 11；CCR11|||CCR 11
CCR-11 is a tannin-containing derivative with antimicrobial activity. CCR-11 inhibits the proliferation of B. subtilis and HeLa cells. CCR-11 inhibits bacterial proliferation and bacterial cytoplasmic division by inhibiting FtsZ assembly and GTPase activity. CCR-11 has potential anti-tumor activity and can be used to study breast cancer and pediatric myelodysplasia.
价 格：￥电议型 号：T25214产 地：中国大陆
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T25213CCG-120304；化合物 T25213ST076528|||ST-076528|||TonB-IN-120304；ST076528|||ST-076528|||TonB-IN-120304
CCG-120304 is a TonB function inhibitor.
价 格：￥电议型 号：T25213产 地：中国大陆
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T25212CCCI-01；化合物CCCI-01CCCI 01|||CCCI01|||Centrosome Clustering Chemical Inhibitor-01；CCCI 01|||CCCI01|||
CCCI-01（Centrosome Clustering Chemical Inhibitor-01） is a centrosome cluster inhibitor. CCCI-01 has anticancer activity, induces apoptosis, and can be used in the study of non-cross-resistant anticancer compounds that block centrosome clustering.
价 格：￥电议型 号：T25212产 地：中国大陆
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T25211CC 1014；化合物 T25211CC1014|||CC-1014|||NSC-356885|||NSC356885|||NSC 356885；CC1014|||CC-1014|||NSC-3568
CC 1014 is a polypeptide antibiotic isolated from Penicillium lilacinum that inhibits phosphorylation of ADP, Mg ATPase.
价 格：￥电议型 号：T25211产 地：中国大陆
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T25079Aminopterin N-hydroxysuccinimide ester；化合物 T25079Nhs-aminopterin|||N-Hydroxysuccinimide aminopterin；
Aminopterin N-hydroxysuccinimide ester is an antineoplastic agent with immunosuppressive properties. Aminopterin works as an enzyme inhibitor by competing for the folate binding site of the enzyme dihydrofolate reductase. Its binding affinity for dihydrofolate reductase effectively blocks tetrahydrofolate synthesis.
价 格：￥电议型 号：T25079产 地：中国大陆
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T24933VCC234718；化合物 T24933VCC-234718|||VCC 234718；VCC-234718|||VCC 234718
VCC234718 is an IMPDH inhibitor. VCC234718 showed growth inhibitory activity against Mycobacterium tuberculosis. VCC234718 inhibits Mtb GuaB2 (Ki: 100 nM).
价 格：￥电议型 号：T24933产 地：中国大陆
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T24702Rabacfosadine succinate；化合物 T24702VDC-1101 succinate|||GS-9219 succinate|||VDC 1101 succinate VDC110
Rabacfosadine succinate is the acyclic nucleoside phosphonate PMEG double prodrug.
价 格：￥电议型 号：T24702产 地：中国大陆
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T24631Pheniprazine hydrochloride；化合物 T24631Pheniprazine HCl|||NSC 17766|||CCRIS 1417|||NSC-17766|||NSC1776
Pheniprazine is an irreversible and nonselective monoamine oxidase inhibitor of the hydrazine chemical class. It was also used in the treatment of angina pectoris and schizophrenia.
价 格：￥电议型 号：T24631产 地：中国大陆
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T24562NUCC-555；化合物 T24562NUCC-555
NUCC-555 is a first-in-class antagonist of activin. It opens a completely new approach to inhibiting the activity of TGF-beta receptor superfamily members.
价 格：￥电议型 号：T24562产 地：中国大陆
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T24435MCC-134；化合物 T24435MCC 134|||MCC134；MCC 134|||MCC134
MCC-134 is an inverse agonist for the pancreatic-type ATP-sensitive K(+) channel. It also used as a vascular relaxing agent.
价 格：￥电议型 号：T24435产 地：中国大陆
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T24434MCC1189；化合物 T24434MCC 1189|||MCC-1189；MCC 1189|||MCC-1189
MCC1189 is a first-in-class MFS efflux pump CaMdr1p inhibitor.
价 格：￥电议型 号：T24434产 地：中国大陆
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T24007DM1-MCC；化合物DM1-MCCMCC-DM1；MCC-DM1
DM1-MCC (MCC-DM1) is an anticancer drug DM1 with an MCC linker.
价 格：￥电议型 号：T24007产 地：中国大陆
