CSNpharm

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Csnpharm is committed to providing you with high quality products and outstanding services. We supply over 5000 bioactive compounds in stock, including inhibitors, agonists and natural products for laboratory and scientific use. Csnpharm has always been committed to develop quality products that are validated by NMR, UPLC, LC-MS, GC, Chiral HPLC and so on. We have a professional technical support team for customer service with years of experience in life science. Csnpharm is your reliable partner for scientific research.

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BMS-309403 10mg  | ≥99%

CSNpharm

BMS-309403 is an inhibitor of fatty acid binding protein 4 (FABP4) with Ki of less than 2 nM that decreases fatty acid uptake in adipocytes in vitro.

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BMS-309403 25mg  | ≥99%

CSNpharm

BMS-309403 is an inhibitor of fatty acid binding protein 4 (FABP4) with Ki of less than 2 nM that decreases fatty acid uptake in adipocytes in vitro.

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BMS-5 5mg  | ≥99%

CSNpharm

BMS-5 is a highly selective and potent inhibitor of both LIMK 1 and 2 with IC50 values of 7 and 8 nM, respectively.

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BMS-5 100mg  | ≥99%

CSNpharm

BMS-5 is a highly selective and potent inhibitor of both LIMK 1 and 2 with IC50 values of 7 and 8 nM, respectively.

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BMS-5 50mg  | ≥99%

CSNpharm

BMS-5 is a highly selective and potent inhibitor of both LIMK 1 and 2 with IC50 values of 7 and 8 nM, respectively.

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BMS-5 10mg  | ≥99%

CSNpharm

BMS-5 is a highly selective and potent inhibitor of both LIMK 1 and 2 with IC50 values of 7 and 8 nM, respectively.

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BMS-5 1mg  | ≥99%

CSNpharm

BMS-5 is a highly selective and potent inhibitor of both LIMK 1 and 2 with IC50 values of 7 and 8 nM, respectively.

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BMY 7378 2HCl 250mg  | ≥98%

CSNpharm

BMY 7378 2HCl is a 5-HT1A partial agonist and a high-affinity α1D adrenoceptor antagonist with Ki values of 2, 800 and 600 nM for cloned rat α1D, rat α1A and hamster α1B receptors respectively.

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BMY 7378 2HCl 1g  | ≥98%

CSNpharm

BMY 7378 2HCl is a 5-HT1A partial agonist and a high-affinity α1D adrenoceptor antagonist with Ki values of 2, 800 and 600 nM for cloned rat α1D, rat α1A and hamster α1B receptors respectively.

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BMY 7378 2HCl 100mg  | ≥98%

CSNpharm

BMY 7378 2HCl is a 5-HT1A partial agonist and a high-affinity α1D adrenoceptor antagonist with Ki values of 2, 800 and 600 nM for cloned rat α1D, rat α1A and hamster α1B receptors respectively.

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Boc-NH-PEG1-CH2CH2COOH 100mg  | ≥97%

CSNpharm

Boc-NH-PEG1-CH2CH2COOH is a cleavable (1 unit PEG) ADC linker and also a PEG- and Alkyl/ether-based PROTAC linker can be used in the synthesis of antibody-drug conjugates (ADCs) or PROTACs.

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Boc-NH-PEG4-CH2CH2COOH 100mg  | ≥97%

CSNpharm

Boc-NH-PEG4-CH2CH2COOH is a PEG-based PROTAC linker can be used in the synthesis of PROTAC. Boc-NH-PEG4-CH2CH2COOH is also a cleavable ADC linker used as a linker for antibody-drug conjugates (ADC).

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Boc-Val-Cit-PABA 10mg  | ≥98%

CSNpharm

Linker for Antibody-Drug-Conjugation (ADC). The Val-Cit will specifically be cleaved by catepsin B. As this enzyme is only present in the lysosome the ADC payload will be release only in the cell.

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Boc-Val-Cit-PABA 100mg  | ≥98%

CSNpharm

Linker for Antibody-Drug-Conjugation (ADC). The Val-Cit will specifically be cleaved by catepsin B. As this enzyme is only present in the lysosome the ADC payload will be release only in the cell.

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Boc-Val-Cit-PABA 25mg  | ≥98%

CSNpharm

Linker for Antibody-Drug-Conjugation (ADC). The Val-Cit will specifically be cleaved by catepsin B. As this enzyme is only present in the lysosome the ADC payload will be release only in the cell.

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Boc-Val-Cit-PABA 50mg  | ≥98%

CSNpharm

Linker for Antibody-Drug-Conjugation (ADC). The Val-Cit will specifically be cleaved by catepsin B. As this enzyme is only present in the lysosome the ADC payload will be release only in the cell.

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Bombesin 1mg  | ≥97%

CSNpharm

Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.

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Bombesin 10mg  | ≥97%

CSNpharm

Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.

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Bombesin 25mg  | ≥97%

CSNpharm

Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.

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Bombesin 5mg  | ≥97%

CSNpharm

Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.

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BP897 25mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BP897 5mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BP897 10mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BP897 1mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BP897 50mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BP897 250mg  | ≥99%

CSNpharm

BP897 is a partially selective dopamine D3 receptor agonist (Ki = 0.92 nM) that developed for the study of cocaine addiction.

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BRD 9876 100mg  | ≥95%

CSNpharm

BRD9876 is a selective inhibitor of MM1S growth. It is selective for microtubule bound Eg5 and causes a rapid arrest in G2/M phase.

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