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T17506Azido-PEG3-SSPy；化合物 T17506Azido-PEG3-SSPy
Azido-PEG3-SSPy is a three-unit cleavable polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17506产 地：中国大陆
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T17505Azido-PEG3-SS-NHS；化合物 T17505Azido-PEG3-SS-NHS
Azido-PEG3-SS-NHS is a three-unit polyethylene glycol (PEG) linker functionalized with an azide group, a cleavable disulfide bond, and an N-hydroxysuccinimide ester. It is primarily employed in the synthesis of antibody-drug conjugates (ADCs) [1].
价 格：￥电议型 号：T17505产 地：中国大陆
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T17504Azido-PEG3-S-PEG4-t-butyl ester；化合物 T17504Azido-PEG3-S-PEG4-t-butyl ester
Azido-PEG3-S-PEG4-t-butyl ester is a PEG-based PROTAC linker employed for PROTAC synthesis[1].
价 格：￥电议型 号：T17504产 地：中国大陆
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T17503Azido-PEG3-S-PEG4-propargyl；化合物 T17503Azido-PEG3-S-PEG4-propargyl
Azido-PEG3-S-PEG4-propargyl is a polyethylene glycol (PEG)-based linker that contains the azide group and propargyl functionality. This linker is designed specifically for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T17503产 地：中国大陆
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T17502Azido-PEG3-S-PEG3-azide；化合物 T17502Azido-PEG3-S-PEG3-azide
Azido-PEG3-S-PEG3-azide is a polyethylene glycol (PEG)-derived linker specifically designed for the synthesis of proteolysis targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T17502产 地：中国大陆
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T17501Azido-PEG3-azide1,11-二叠氮基-3,6,9-三氧杂十一烷1,11-二叠氮基-3,6,9-三氧杂十一烷
Azido-PEG3-azide is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
价 格：￥电议型 号：T17501产 地：中国大陆
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T17500Azido-PEG3-amide-C3-triethoxysilane；化合物 T17500Azido-PEG3-amide-C3-triethoxysilane
Azido-PEG3-amide-C3-triethoxysilane is a polyethylene glycol (PEG)-based linker specifically designed for use in the synthesis of Proteolysis Targeting Chimeras (PROTACs)[1].
价 格：￥电议型 号：T17500产 地：中国大陆
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T1750Pirodavir；吡罗达韦R77975；R77975|||吡罗达韦
Pirodavir (R77975) (R 77975), the prototype of broad-spectrum anti-picornavirus compounds, is a potent human rhinovirus (HRV) capsid-binding inhibitor.
价 格：￥电议型 号：T1750产 地：中国大陆
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T16773Ro 90-7501化合物Ro 90-7501RO-90-7501
Ro 90-7501 is an amyloid β42 (Aβ42) protofibrillar and TPR-dependent PP5 inhibitor, a novel radiosensitiser for cervical cancer cells, which inhibits ATM phosphorylation, promotes apoptosis, and induces cell-cycle arrest.Ro 90-7501 exhibits antiviral activity and potential anticancer activity by inhibiting ATM phosphorylation and DNA repair, and by inhibiting HCMV.
价 格：￥电议型 号：T16773产 地：中国大陆
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T16766Ro 08-2750；化合物Ro 08-2750Ro 08-2750
Ro 08-2750 is a non-peptide and reversible nerve growth factor (NGF) inhibitor which binds to NGF, and with an IC50 of ~ 1 ?M. Ro 08-2750 is a selective MSI RNA-binding activity inhibitor, with an IC50 of 2.7 μM. Ro 08-2750 inhibits NGF binding to p75NTR selectively over TRKA.
价 格：￥电议型 号：T16766产 地：中国大陆
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T16750Rigosertib；瑞格色替ON-01910；ON-01910|||瑞格色替
Rigosertib (ON-01910) is a selective and non-ATP-competitive inhibitor of PLK1 (IC50: 9 nM). Rigosertib is a multi-kinase inhibitor and a selective anti-cancer agent, which induces apoptosis by inhibition of the PI3 kinase/Akt pathway, promotes the phosphorylation of histone H2AX and induces G2/M arrest in the cell cycle.
价 格：￥电议型 号：T16750产 地：中国大陆
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T16515PF 750；化合物PF 750PF-750|||UNII-7756CPP14K|||ZINC27647189；PF-750|||UNII-7756CPP14K|||ZINC27647189
PF 750 (ZINC27647189) is a selective and covalent inhibitor of FAAH. PF 750 shows IC50s varying from 16.2 to 595 nM in different incubation times.
价 格：￥电议型 号：T16515产 地：中国大陆
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T15630Tilmacoxib；替马考昔RWJ57504|||JTP19605|||JTE522；RWJ57504|||JTP19605|||替马考昔|||JTE522
Tilmacoxib is a highly selective, time-dependent, and irreversible inhibitor of human COX-2 ( IC50: 85 nM in an enzyme assay).
价 格：￥电议型 号：T15630产 地：中国大陆
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T14750Boc-NH-PEG6-amine；化合物 T14750Boc-NH-PEG6-amine
Boc-NH-PEG6-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T14750产 地：中国大陆
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T14380AZD7507；化合物CS-2850AZD7507
AZD7507 is a CSF-1R inhibitor with an IC50 of 32 nM. AZD7507 has antitumor activity.
价 格：￥电议型 号：T14380产 地：中国大陆
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T13750L-Fucitol；L-岩藻糖醇1-Deoxy-D-galactitol；L-岩藻糖醇|||1-Deoxy-D-galactitol
L-Fucitol (1-Deoxy-D-galactitol) is a galactitol analogue isolated from Myristica fragrans (Nutmeg), inhibits galactitol-positive strains of Escherichia coli K12.
价 格：￥电议型 号：T13750产 地：中国大陆
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T12750ROR agonist-1；化合物 T12750ROR agonist-1
ROR agonist-1 is a potent and orally bioavailable the retinoic acid receptor-related orphan receptor C2 (RORC2) inverse agonist(inhibition of IL-17A production from human primary TH 17 cells with a pIC50 of 7.5).
价 格：￥电议型 号：T12750产 地：中国大陆
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T125750Lignicol；化合物 LignicolLignicol
Lignicol is a useful organic compound for research related to life sciences. The catalog number is T125750 and the CAS number is 153765-43-6.
价 格：￥电议型 号：T125750产 地：中国大陆
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T12475014,15-Didehydroisoeburnamine；化合物 14,15-Didehydroisoeburnamine14,15-Didehydroisoeburnamine
14,15-Didehydroisoeburnamine is a useful organic compound for research related to life sciences and the catalog number is T124750.
价 格：￥电议型 号：T124750产 地：中国大陆
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T11750LKDOAM-25 trihydrochloride (2230731-99-2 free base)；化合物 T11750LKDOAM-25 trihydrochloride；KDOAM-25 tri
KDOAM-25 trihydrochloride increases global H3K4 methylation at transcriptional start sites and impairs proliferation in multiple myeloma MM1S cells. KDOAM-25 trihydrochloride is a potent and highly selective histone lysine demethylases 5 (KDM5) inhibitor with IC50s of 71 nM, 19 nM, 69 nM, 69 nM for KDM5A, KDM5B, KDM5C, KDM5D, respectively.
价 格：￥电议型 号：T11750L产 地：中国大陆
