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T15336Fonadelpar；化合物 T15336SJP0035|||Fonadelpar|||SJP-0035|||NPS005|||SJP 0035|||NPS-005|||NPS-005|||Fonad
Fonadelpar is an agonist of PPARδ. It also is used in the research of neuroparalytic keratopathy.
价 格：￥电议型 号：T15336产 地：中国大陆
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T15335FN-1501；化合物FN-1501FN-1501
FN-1501 is a potent FLT3 and CDK inhibitor (IC50s: 2.47, 0.85, 1.96, and 0.28 nM for CDK2/cyclin A, CDK4/cyclin D1, CDK6/cyclin D1 and FLT3, respectively). FN-1501 also has anticancer activity.
价 格：￥电议型 号：T15335产 地：中国大陆
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T15334Fmoc-PEG6-NHS ester；化合物 T15334Fmoc-PEG6-NHS ester
Fmoc-PEG6-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：T15334产 地：中国大陆
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T15333Fmoc-PEG5-NHS ester；化合物 T15333Fmoc-PEG5-NHS ester
Fmoc-PEG5-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：T15333产 地：中国大陆
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T15332Fmoc-PEG4-NHS ester；化合物 T15332Fmoc-PEG4-NHS ester
Fmoc-PEG4-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：T15332产 地：中国大陆
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T15331Fmoc-PEG4-Ala-Ala-Asn-PAB；化合物 T15331Fmoc-PEG4-Ala-Ala-Asn-PAB
Fmoc-PEG4-Ala-Ala-Asn-PAB is a four-unit polyethylene glycol (PEG) linker, cleavable in nature. It is specifically employed for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15331产 地：中国大陆
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T15330Fmoc-PEG3-C2-NHS ester；化合物 T15330Fmoc-PEG3-C2-NHS ester
Fmoc-PEG3-CH2CH2-NHS ester is a PEG-based linker derived from fluorenylmethoxycarbonyl (Fmoc), which is used as a moiety for the efficient synthesis of PROTACs (proteolysis-targeting chimeras)[1]. This compound offers a practical solution for connecting desired molecules and targeting specific proteins for degradation.
价 格：￥电议型 号：T15330产 地：中国大陆
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T1533Valganciclovir hydrochloride；缬更昔洛韦盐酸盐Valganciclovir HCl|||Valcyt|||Valcyte；Valganciclovir HCl|||Valc
Valganciclovir hydrochloride (Valganciclovir HCl) is a hydrochloride salt form of valganciclovir, a prodrug form of ganciclovir, a nucleoside analog of 2´-deoxyguanosine, with antiviral activity. After phosphorylation, valganciclovir is incorporated into DNA, resulting in inhibition of viral DNA polymerase, and viral replication.
价 格：￥电议型 号：T1533产 地：中国大陆
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T15329Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB；化合物 T15329Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB
Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB is a cleavable three-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15329产 地：中国大陆
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T15328Fmoc-PEG2-C2-NHS ester；化合物 T15328Fmoc-PEG2-C2-NHS ester
Fmoc-PEG2-CH2CH2-NHS ester is a polyethylene glycol (PEG)-based PROTAC linker designed for the synthesis of proteolysis targeting chimeras (PROTACs).
价 格：￥电议型 号：T15328产 地：中国大陆
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T15327Fmoc-PEG1-CH2CH2-NHS ester；化合物 T15327Fmoc-PEG1-CH2CH2-NHS ester
Fmoc-PEG1-CH2CH2-NHS ester is a polyethylene glycol (PEG) derived linker specifically designed for the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
价 格：￥电议型 号：T15327产 地：中国大陆
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T15326Fmoc-NMe-PEG4-C2-acid；化合物 T15326Fmoc-NMe-PEG4-C2-acid
Fmoc-NMe-PEG4-C2-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：T15326产 地：中国大陆
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T15325Fmoc-NH-PEG9-CH2CH2COOH；化合物 T15325Fmoc-NH-PEG9-CH2CH2COOH
Fmoc-NH-PEG9-CH2CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15325产 地：中国大陆
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T15324Fmoc-NH-PEG8-NHS esterFMOC-N-酰氨基-DPEG(R)8-NHS酯FMOC-N-酰氨基-DPEG(R)8-NHS酯
Fmoc-NH-PEG8-NHS ester is a PEG-based PROTAC linker that can be used in PROTAC synthesis[1].
价 格：￥电议型 号：T15324产 地：中国大陆
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T15323Fmoc-NH-PEG8-CH2COOH；化合物 T15323Fmoc-NH-PEG8-CH2COOH
Fmoc-NH-PEG8-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15323产 地：中国大陆
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T15322Fmoc-NH-PEG8-CH2CH2COOH；化合物 T15322Fmoc-NH-PEG8-CH2CH2COOH
Fmoc-NH-PEG8-CH2CH2COOH is a cleavable linker employed for ADC synthesis, primarily in the formation of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15322产 地：中国大陆
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T15321Fmoc-NH-PEG6-CH2COOH；化合物 T15321Fmoc-NH-PEG6-CH2COOH
Fmoc-NH-PEG6-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15321产 地：中国大陆
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T15320Fmoc-NH-PEG6-CH2CH2COOH；化合物 T15320Fmoc-NH-PEG6-CH2CH2COOH
Fmoc-NH-PEG6-CH2CH2COOH is a cleavable linker commonly employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15320产 地：中国大陆
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T1532Pidotimod；匹多莫德Pidotimod
Pidotimod is a synthetic dipeptide with immunomodulatory properties.
价 格：￥电议型 号：T1532产 地：中国大陆
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T15319Fmoc-NH-PEG5-CH2COOH；化合物 T15319Fmoc-NH-PEG5-CH2COOH
Fmoc-NH-PEG5-CH2COOH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15319产 地：中国大陆
