Search Results

Taselisib 5 mg  | 99.46%

TargetMol

Taselisib is an orally bioavailable inhibitor of the class I phosphatidylinositol 3-kinase (PI3K) alpha isoform (PIK3CA), with potential antineoplastic activity.

More Information Supplier Page

Taselisib 50 mg  | 99.46%

TargetMol

Taselisib is an orally bioavailable inhibitor of the class I phosphatidylinositol 3-kinase (PI3K) alpha isoform (PIK3CA), with potential antineoplastic activity.

More Information Supplier Page

Taselisib 10 mg  | 99.46%

TargetMol

Taselisib is an orally bioavailable inhibitor of the class I phosphatidylinositol 3-kinase (PI3K) alpha isoform (PIK3CA), with potential antineoplastic activity.

More Information Supplier Page

(S)-P7C3-OMe 5 mg  | 99.61%

TargetMol

(S)-P7C3-OMe is a methoxy derivative of parent compound P7C3, an aminopropyl carbazole that exhibits antidepressant and neuroprotective activities.

More Information Supplier Page

(S)-P7C3-OMe 50 mg  | 99.61%

TargetMol

(S)-P7C3-OMe is a methoxy derivative of parent compound P7C3, an aminopropyl carbazole that exhibits antidepressant and neuroprotective activities.

More Information Supplier Page

(S)-P7C3-OMe 2 mg  | 99.61%

TargetMol

(S)-P7C3-OMe is a methoxy derivative of parent compound P7C3, an aminopropyl carbazole that exhibits antidepressant and neuroprotective activities.

More Information Supplier Page

(S)-P7C3-OMe 25 mg  | 99.61%

TargetMol

(S)-P7C3-OMe is a methoxy derivative of parent compound P7C3, an aminopropyl carbazole that exhibits antidepressant and neuroprotective activities.

More Information Supplier Page

U-104 10 mg  | 100.00%

TargetMol

U-104 (NSC-213841) is an effective carbonic anhydrase (CA) inhibitor for CA IX( Ki=45.1 nM) and CA XII(Ki=4.5 nM).

More Information Supplier Page

U-104 25 mg  | 100.00%

TargetMol

U-104 (NSC-213841) is an effective carbonic anhydrase (CA) inhibitor for CA IX( Ki=45.1 nM) and CA XII(Ki=4.5 nM).

More Information Supplier Page

WHI-P258 50 mg  | 99.59%

TargetMol

WHI-P258 is a dimethoxyquinazoline inhibitor of JAK3. This compound binds JAK3 weakly and may be used as a JAK-binding negative control in the development of new therapeutics.

More Information Supplier Page