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SCR7 25mg 25mg  | Purity Not Available

Adooq Bioscience

SCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in tumour regression by activation of p53 mediated apoptosis.

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SCR7 10mg 10mg  | Purity Not Available

Adooq Bioscience

SCR7 is a specific DNA Ligase IV inhibitor. SCR7 inhibits end joining of double strand breaks in diverse cell types resulting in tumour regression by activation of p53 mediated apoptosis.

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K-7174 2HCl 5mg 5mg  | Purity Not Available

Adooq Bioscience

K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

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K-7174 2HCl 25mg 25mg  | Purity Not Available

Adooq Bioscience

K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

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K-7174 2HCl 10mg 10mg  | Purity Not Available

Adooq Bioscience

K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

More Information Supplier Page

K-7174 5mg 5mg  | Purity Not Available

Adooq Bioscience

K-7174 is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

More Information Supplier Page

K-7174 25mg 25mg  | Purity Not Available

Adooq Bioscience

K-7174 is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

More Information Supplier Page

K-7174 10mg 10mg  | Purity Not Available

Adooq Bioscience

K-7174 is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

More Information Supplier Page

SGC 707 10mg 10mg  | Purity Not Available

Adooq Bioscience

SGC 707 is a potent allosteric inhibitor of PRMT3 (IC50 = 50 nM) with >100-fold selectivity over other methyltransferases and other non-epigenetic targets.

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