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T1780Parecoxib；帕瑞昔布SC 69124|||Vorth-P|||Valus-P；SC 69124|||帕瑞昔布|||Vorth-P|||Valus-P
Parecoxib (SC 69124) is an effective and selective COX-2 inhibitor.
价 格：￥电议型 号：T1780产 地：中国大陆
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T17789DBCO-(PEG2-VC-PAB-MMAE)2；化合物 T17789DBCO-(PEG-2-VC-PAB-MMAE)2|||DBCO(PEG2VCPABMMAE)2|||DBCO-(PEG2-VC-
DBCO-(PEG2-VC-PAB-MMAE)2 consists of Monomethyl auristatin E (MMAE), a toxin payload in antibody-drug conjugate [1], conjugated to the cleavable linker DBCO-(PEG2-VC-PAB)2. MMAE, a potent tubulin inhibitor, serves as the cytotoxic component in this formulation.
价 格：￥电议型 号：T17789产 地：中国大陆
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T17788DBCO-(PEG2-Val-Cit-PAB)2；化合物 T17788DBCO-(PEG2-Val-Cit-PAB)2
DBCO-(PEG2-Val-Cit-PAB)2 is a dual cleavable ADC linker for antibody-drug conjugates (ADCs).
价 格：￥电议型 号：T17788产 地：中国大陆
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T17787DBCO-PEG2-NH-Boc；化合物 T17787DBCO-PEG2-NH-Boc
DBCO-PEG2-NH-Boc 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：T17787产 地：中国大陆
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T17786DBCO-PEG2-amine；化合物 T17786DBCO-PEG2-amine
DBCO-PEG2-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：T17786产 地：中国大陆
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T17785DBCO-PEG2-acid；化合物 T17785DBCO-PEG2-acid
DBCO-PEG2-acid 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：T17785产 地：中国大陆
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T17784DBCO-PEG13-DBCO；化合物 T17784DBCO-PEG13-DBCO
DBCO-PEG13-DBCO 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：T17784产 地：中国大陆
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T17783DBCO-PEG12-NHS ester；化合物 T17783DBCO-PEG12-NHS ester
DBCO-PEG12-NHS ester 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：T17783产 地：中国大陆
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T17782DBCO-PEG12-acid；化合物 T17782DBCO-PEG12-acid
DBCO-PEG12-acid 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：T17782产 地：中国大陆
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T17781DBCO-PEG10-DBCO；化合物 T17781DBCO-PEG10-DBCO
DBCO-PEG10-DBCO 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：T17781产 地：中国大陆
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T17780DBCO-PEG1；化合物 T17780DBCO-PEG1
DBCO-PEG1 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：T17780产 地：中国大陆
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T1778AT7519 Hydrochloride；化合物AT 7519 hydrochloride saltAT7519 HCl|||AT 7519 hydrochloride salt；AT7519 HCl
AT7519 Hydrochloride (AT7519 HCl) is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9.
价 格：￥电议型 号：T1778产 地：中国大陆
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T17778DBCO-PEG1-NH-Boc；化合物 T17778DBCO-PEG1-NH-Boc
DBCO-PEG1-NH-Boc 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：T17778产 地：中国大陆
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T17678Boc-NH-PEG36-CH2CH2COOH；化合物 T17678Boc-NH-PEG36-CH2CH2COOH
Boc-NH-PEG36-CH2CH2COOH is a polyethylene glycol (PEG)-based PROTAC linker employed for the synthesis of PROTACs[1].
价 格：￥电议型 号：T17678产 地：中国大陆
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T17578Biotin-PEG36-PFP ester；化合物 T17578Biotin-PEG36-PFP ester
Biotin-PEG36-PFP ester 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：T17578产 地：中国大陆
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T17478Azido-PEG1-Val-Cit-OH；化合物 T17478Azido-PEG1-Val-Cit-OH
Azido-PEG1-Val-Cit-OH is a one-unit cleavable PEG ADC linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T17478产 地：中国大陆
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T17378Ald-Ph-amido-C2-nitrate；化合物 T17378Ald-Ph-amido-C2-nitrate
Ald-Ph-amido-C2-nitrate (Example XXIVb) is a thiazolidine derivative primarily employed as a noncleavable ADC linker[1].
价 格：￥电议型 号：T17378产 地：中国大陆
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T17278YUKA1；化合物 T17278YUKA1
YUKA1 is a potent and cell-permeable Lysine demethylase 5A inhibitor (IC50: 2.66 μM) and less active on KDM5C (IC50, 7.12 μM). YUKA1 is inactive on KDM5B, KDM6A, or KDM6B.
价 格：￥电议型 号：T17278产 地：中国大陆
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T17225Vercirnon；维塞诺CCX282-B|||GSK-1605786|||Traficet-EN；CCX282-B|||维塞诺|||GSK-1605786|||Traficet-EN
Vercirnon (Traficet-EN) is a selective and potent antagonist of CCR9 (IC50: 10 nM). It is also used in the research of inflammatory bowel diseases.
价 格：￥电议型 号：T17225产 地：中国大陆
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T17178Tulopafant；妥洛帕泛RP 59227；RP 59227
Tulopafant (RP 59227) is a potent platelet-activating factor (PAF) antagonist that increases capillary patency and prolongs allograft heart survival.
价 格：￥电议型 号：T17178产 地：中国大陆
