PMSF
250mg
| ≥95%
CSNpharm
PMSF
100mg
| ≥95%
CSNpharm
CSNpharm
Pneumocandin B0 is used to synthesize caspofungin. It is a strong antifungal working by inhibiting the synthesis of β-(1→3)-D-glucan, which is a fundamental component in most cell walls
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CSNpharm
Pneumocandin B0 is used to synthesize caspofungin. It is a strong antifungal working by inhibiting the synthesis of β-(1→3)-D-glucan, which is a fundamental component in most cell walls
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CSNpharm
Pneumocandin B0 is used to synthesize caspofungin. It is a strong antifungal working by inhibiting the synthesis of β-(1→3)-D-glucan, which is a fundamental component in most cell walls
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PNPP
1g
| ≥99%
CSNpharm
CSNpharm
PNU112455A HCl is an ATP site competetive inhibitor of CDK2 and CDK5. The Km for binding to the ATP site of CDK2 and CDK5 is 3.6 and 3.3 mM, respectively.
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CSNpharm
PNU112455A HCl is an ATP site competetive inhibitor of CDK2 and CDK5. The Km for binding to the ATP site of CDK2 and CDK5 is 3.6 and 3.3 mM, respectively.
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CSNpharm
PNU112455A HCl is an ATP site competetive inhibitor of CDK2 and CDK5. The Km for binding to the ATP site of CDK2 and CDK5 is 3.6 and 3.3 mM, respectively.
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CSNpharm
PNU-282987 is a selective α7 nAChR agonist with ki value of 26nM and displays almost no effect on α1β1γδ and α3β4 nAChRs.
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CSNpharm
PNU-282987 is a selective α7 nAChR agonist with ki value of 26nM and displays almost no effect on α1β1γδ and α3β4 nAChRs.
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CSNpharm
PNU-282987 is a selective α7 nAChR agonist with ki value of 26nM and displays almost no effect on α1β1γδ and α3β4 nAChRs.
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CSNpharm
PNU-282987 is a selective α7 nAChR agonist with ki value of 26nM and displays almost no effect on α1β1γδ and α3β4 nAChRs.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Podocarpusflavone A is a DNA topoisomerase I inhibitor isolated and purified from the barks of Podocarpus macrophyllus, and is the strongest noncytotoxic non-nucleotide molecule exhibiting a specific inhibitory activity against the RNA polymerase domain of DV-NS5 and thus is promising for chemotherapy development against dengue fever.
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CSNpharm
Podocarpusflavone A is a DNA topoisomerase I inhibitor isolated and purified from the barks of Podocarpus macrophyllus, and is the strongest noncytotoxic non-nucleotide molecule exhibiting a specific inhibitory activity against the RNA polymerase domain of DV-NS5 and thus is promising for chemotherapy development against dengue fever.
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CSNpharm
Podocarpusflavone A is a DNA topoisomerase I inhibitor isolated and purified from the barks of Podocarpus macrophyllus, and is the strongest noncytotoxic non-nucleotide molecule exhibiting a specific inhibitory activity against the RNA polymerase domain of DV-NS5 and thus is promising for chemotherapy development against dengue fever.
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CSNpharm
CSNpharm
CSNpharm
Poloxime is an analogue of thymoquinone, which bind to the phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1.
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CSNpharm
Poloxime is an analogue of thymoquinone, which bind to the phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1.
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CSNpharm
Poloxime is an analogue of thymoquinone, which bind to the phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1.
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CSNpharm
Poloxime is an analogue of thymoquinone, which bind to the phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1.
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CSNpharm
Poloxime is an analogue of thymoquinone, which bind to the phosphoserine/phosphothreonine recognition site of the polo-box domain of polo-like kinase 1.
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CSNpharm
Polydatin, extracted from the roots ofPolygonum cuspidatumSieb, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models.
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CSNpharm
Polydatin, extracted from the roots ofPolygonum cuspidatumSieb, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models.
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CSNpharm
Polydatin, extracted from the roots ofPolygonum cuspidatumSieb, a widely used traditional Chinese remedies, possesses anti-inflammatory activity in several experimental models.
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CSNpharm
Polydatin(Random Configuration) is a natural precursor and glycoside form of resveratrol with anti-inflammatory and anti-oxidative activities.
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CSNpharm
Polydatin(Random Configuration) is a natural precursor and glycoside form of resveratrol with anti-inflammatory and anti-oxidative activities.
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CSNpharm
Polydatin(Random Configuration) is a natural precursor and glycoside form of resveratrol with anti-inflammatory and anti-oxidative activities.
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CSNpharm
CSNpharm
CSNpharm
CSNpharm
CSNpharm
Pomalidomide-C2-Amine is a PROTAC block consist of Pomalidomide linked to alkyl with an Amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-C2-Amine is a PROTAC block consist of Pomalidomide linked to alkyl with an Amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-C2-Amine is a PROTAC block consist of Pomalidomide linked to alkyl with an Amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-C2-Amine is a PROTAC block consist of Pomalidomide linked to alkyl with an Amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-PEG4-C2-Amine is a PROTAC block consist of Pomalidomide and a linker with an amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-PEG4-C2-Amine is a PROTAC block consist of Pomalidomide and a linker with an amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-PEG4-C2-Amine is a PROTAC block consist of Pomalidomide and a linker with an amine functional group for conjugation reactions.
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CSNpharm
Pomalidomide-PEG4-C2-Amine is a PROTAC block consist of Pomalidomide and a linker with an amine functional group for conjugation reactions.
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