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T16700QC6352QC6352
QC6352 is a selective and effective KDM4C inhibitor (IC50: 35 nM).
价 格：￥电议型 号：T16700产 地：美洲
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T17654Boc-NH-C6-BrBoc-NH-C6-Br
Boc-NH-C6-Br is a cleavable linker used for antibody-drug conjugates (ADC)[1].
价 格：￥电议型 号：T17654产 地：美洲
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T1982TriapineTriapine,NSC663249,OCX191
Triapine is a novel inhibitor of the M2 subunit of ribonucleotide reductase (RR).
价 格：￥电议型 号：T1982产 地：美洲
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T1983CAY10603CAY10603,BML-281,HDAC6 Inhibitor
CAY10603 is a potent and selective inhibitor of HDAC6.
价 格：￥电议型 号：T1983产 地：美洲
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T2252UNC669UNC669
UNC669 is an effective and specific MBT (malignant brain tumor) inhibitor with IC50 of 4.2/3.1 uM for L3MBTL1/3.
价 格：￥电议型 号：T2252产 地：美洲
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T2452C646C646
C646, a histone acetyltransferase inhibitor, inhibits p300 (Ki: 400 nM, in a cell-free assay).
价 格：￥电议型 号：T2452产 地：美洲
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T5538DC661DC661
DC661 is palmitoyl-protein thioesterase 1 (PPT1) inhibitor, inhibits autophagy, and acts as an anti-lysosomal agent. Anti-cancer activity
价 格：￥电议型 号：T5538产 地：美洲
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T5854AM580AM580,CD336,NSC608001
AM580 is a retinoic acid receptor agonist that is selective for RARα( IC50 : 8 nM )
价 格：￥电议型 号：T5854产 地：美洲
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T5S1131Ganoderic acid C6Ganoderic acid C6
1. Ganoderic acid C6 has antinociceptive activity.
价 格：￥电议型 号：T5S1131产 地：美洲
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T832736′-Hydroxyjusticidin C；化合物 6′-Hydroxyjusticidin C6′-Hydroxyjusticidin C
6′-Hydroxyjusticidin C, a lignan, is extractable from Justicia procumbens [1].
价 格：￥电议型 号：T83273产 地：中国大陆
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T832726′-O-β-D-Glucopyranosylphlorigidoside C；化合物 6′-O-β-D-Glucopyranosylphlorigidoside C6′-O-β-D-Glucopyr
Compound 1, known as 6′-O-β-D-Glucopyranosylphlorigidoside C, is an iridoid glycoside extractable from the plant Lamiophlomis rotata [1].
价 格：￥电议型 号：T83272产 地：中国大陆
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T82989AP-C6；化合物 AP-C6AP-C6
AP-C6 is a potent inhibitor of guanosine 3´,5´-cyclic monophosphate (cGMP)-dependent protein kinase II (cGKII), exhibiting a pIC50 of 6.5. It inhibits human cGKII activity in vitro in a concentration-dependent manner and potentiates cAMP signaling through phosphodiesterase (PDE) inhibition [1].
价 格：￥电议型 号：T82989产 地：中国大陆
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T82795C6-Amide-(PEG)n-CH3；化合物 C6-Amide-(PEG)n-CH3C6-Amide-(PEG)n-CH3
C6-Amide-(PEG)n-CH3 (n=310), an active compound utilized for PEGylation in Egaptivon pegol, is a small molecule crucial for researching platelet dysfunction disorders [1].
价 格：￥电议型 号：T82795产 地：中国大陆
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T82794C6-NBD Sphinganine；化合物 C6-NBD SphinganineC6-NBD Sphinganine
C6-NBD Sphinganine, a fluorescent sphinganine analog, serves as a dye for labeling fatty acids [1].
价 格：￥电议型 号：T82794产 地：中国大陆
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T82600DDAO-C6；化合物 DDAO-C6DDAO-C6
DDAO-C6, a cridone ester derivative, serves as a highly specific fluorescent probe for detecting human serum albumin (HSA). Additionally, it functions as an enzymatically activatable near-infrared fluorescent probe, facilitating the visual detection of endogenous lipase produced by gut microbes (Ex/Em=600/658 nm) [1] [2].
价 格：￥电议型 号：T82600产 地：中国大陆
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T82226HDAC6-IN-21；化合物 HDAC6-IN-21HDAC6-IN-21
HDAC6-IN-21 (compound 13) is an irreversible inhibitor of histone deacetylase 6 (HDAC6) [1].
价 格：￥电议型 号：T82226产 地：中国大陆
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T82225HDAC6-IN-24；化合物 HDAC6-IN-24HDAC6-IN-24
HDAC6-IN-24 (compound N1) is an inhibitor of histone deacetylase 6 (HDAC6) [1].
价 格：￥电议型 号：T82225产 地：中国大陆
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T82224HDAC6-IN-25；化合物 HDAC6-IN-25HDAC6-IN-25
HDAC6-IN-25 (compound 8) is a potent and selective HDAC6 inhibitor, exhibiting an IC50 value of 0.6 nM [1].
价 格：￥电议型 号：T82224产 地：中国大陆
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T81832MC-VC-PABC-C6-alpha-Amanitin；化合物 MC-VC-PABC-C6-alpha-AmanitinMC-VC-PABC-C6-alpha-Amanitin
MC-VC-PABC-C6-alpha-Amanitin is an antibody-drug conjugate that combines the anticancer toxin alpha-Amanitin with the monoclonal antibody MC-VC-PABC-C6. Alpha-Amanitin acts as a potent inhibitor of RNA polymerase IIα, enabling the conjugate to selectively target and recognize HER2-positive tumor cells. This specificity makes MC-VC-PABC-C6-alpha-Amanitin a valuable research tool in the study of breast and gastric cancers [1].
价 格：￥电议型 号：T81832产 地：中国大陆
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T81422Pomalidomid-C6-PEG3-butyl-N3；化合物 Pomalidomid-C6-PEG3-butyl-N3Pomalidomid-C6-PEG3-butyl-N3
Pomalidomid-C6-PEG3-butyl-N3 is a click chemistry reagent featuring an azide group and serves as a crosslinker-E3 ligase ligand conjugate. This compound is utilized as a click-reactive protein degrader building block within PROTAC research and as a template for the synthesis of targeted protein degraders [1].
价 格：￥电议型 号：T81422产 地：中国大陆
