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T18719SPP;化合物 SPPSPP
SPP is a cleavable linker that can be used to form antibody-coupled compounds with therapeutic effects on cancer.
价 格:¥电议型 号:T18719产 地:中国大陆
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T18718SPP-DM1;化合物 T18718SPP-DM1
SPP-DM1, a drug-linker conjugate for antibody-drug conjugates (ADC), demonstrates potent antitumor activity. It comprises DM1 (a potent microtubule-disrupting agent) connected through the ADC linker SPP[1].
价 格:¥电议型 号:T18718产 地:中国大陆
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T18717SPDV;化合物 T18717SPDV
SPDV is a cleavable antibody-drug conjugate (ADC) linker utilized in the diagnostic and therapeutic management of cancer and B cell proliferative diseases.
价 格:¥电议型 号:T18717产 地:中国大陆
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T18716SPDP-PEG9-acid;化合物 T18716SPDP-PEG9-acid
SPDP-PEG9-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:T18716产 地:中国大陆
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T18715SPDP-PEG7-acid;化合物 T18715SPDP-PEG7-acid
SPDP-PEG7-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:T18715产 地:中国大陆
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T18714SPDP-PEG5-acid;化合物 T18714SPDP-PEG5-acid
SPDP-PEG5-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:T18714产 地:中国大陆
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T18713SPDP-PEG36-NHS ester;化合物 T18713SPDP-PEG36-NHS ester
SPDP-PEG36-NHS ester is a PEG ADC linker consisting of 36 units, characterized by cleavability. It plays a crucial role in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格:¥电议型 号:T18713产 地:中国大陆
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T18712SPDP-PEG24-NHS ester;化合物 T18712SPDP-PEG24-NHS ester
SPDP-PEG24-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:T18712产 地:中国大陆
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T18711SPDP-PEG24-acid;化合物 T18711SPDP-PEG24-acid
SPDP-PEG24-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:T18711产 地:中国大陆
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T18710SPDP-PEG12-NHS ester;化合物 T18710SPDP-PEG12-NHS ester
SPDP-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:T18710产 地:中国大陆
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T18709SPDP-PEG12-acid;化合物 T18709SPDP-PEG12-acid
SPDP-PEG12-acid is a cleavable 12-unit polyethylene glycol (PEG) linker utilized for the synthesis of antibody-drug conjugates (ADCs)[1].
价 格:¥电议型 号:T18709产 地:中国大陆
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T18708SPDP-C6-Gly-Leu-NHS ester;化合物 T18708SPDP-C6-Gly-Leu-NHS ester
SPDP-C6-Gly-Leu-NHS ester is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格:¥电议型 号:T18708产 地:中国大陆
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T18707SPDMV;化合物 SPDMVSPDMV
SPDMV is a PEG-based ADC linker involved in the synthesis of antibody-coupled reactive molecules (ADCs).
价 格:¥电议型 号:T18707产 地:中国大陆
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T18706SPDMV-sulfo;化合物 T18706SPDMV-sulfo
SPDMV-sulfo, a glutathione-cleavable ADC linker, facilitates the release of drugs from antibody-drug conjugates (ADCs).
价 格:¥电议型 号:T18706产 地:中国大陆
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T18705SPDMB;化合物 T18705SPDMB
SPDMB is a glutathione cleavable ADC linker used for the antibody-drug conjugate (ADCs).
价 格:¥电议型 号:T18705产 地:中国大陆
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T18704SPDH;化合物 T18704SPDH
SPDH is a cleavable antibody-drug conjugate (ADC) linker utilized for the diagnosis and therapy of cancer as well as B cell proliferative diseases.
价 格:¥电议型 号:T18704产 地:中国大陆
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T18703SPDB-sulfo;化合物 T18703SPDB-sulfo
SPDB-sulfo, a glutathione-cleavable linker, is utilized in the development of antibody-drug conjugates (ADCs) [1].
价 格:¥电议型 号:T18703产 地:中国大陆
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T18701SPDB-DM4;化合物 T18701SPDB-DM4
SPDB-DM4 is a drug-linker conjugate designed for antibody-drug conjugate (ADC) applications, employing the maytansine-based payload DM4 (a tubulin inhibitor) connected through a SPDB linker. This compound demonstrates significant anti-tumor efficacy.
价 格:¥电议型 号:T18701产 地:中国大陆
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T18621Tos-PEG1-O-CH2COOH;化合物 T18621PROTAC Linker 28|||PROTAC Linker 28|||Tos PEG1 O CH2COOH|||TosPEG1OCH2C
Tos-PEG1-O-CH2COOH (PROTAC Linker 28), a PEG-based PROTAC linker, finds applicability in PROTACs synthesis [1].
价 格:¥电议型 号:T18621产 地:中国大陆
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T18588Propargyl-PEG5-Ms;化合物Propargyl-PEG5-MsPropargyl-PEG6-Ms;Propargyl-PEG6-Ms
Propargyl-PEG5-Ms (Propargyl-PEG6-Ms) is a PEG-based PROTAC linker. Propargyl-PEG5-Ms can be used in the synthesis of PROTACs.
价 格:¥电议型 号:T18588产 地:中国大陆