CSNpharm
BYK204165 is a potent and selective poly(ADP-ribose) polymerase (PARP)-1 inhibitor (pIC50 values are 5.38 and 7.35 for PARP-2 and PARP-1 respectively).
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CSNpharm
CSNpharm
CSNpharm
C-176
5mg
| ≥99%
CSNpharm
C-176 is a STING inhibitor with anti-inflammatory effect. It blocks the palmitoylation of STING by covalently targeting the transmembrane cysteine residue 91.
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C-176
50mg
| ≥99%
CSNpharm
C-176 is a STING inhibitor with anti-inflammatory effect. It blocks the palmitoylation of STING by covalently targeting the transmembrane cysteine residue 91.
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C-176
100mg
| ≥99%
CSNpharm
C-176 is a STING inhibitor with anti-inflammatory effect. It blocks the palmitoylation of STING by covalently targeting the transmembrane cysteine residue 91.
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C-176
10mg
| ≥99%
CSNpharm
C-176 is a STING inhibitor with anti-inflammatory effect. It blocks the palmitoylation of STING by covalently targeting the transmembrane cysteine residue 91.
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CSNpharm
CSNpharm
C-82
1mg
| ≥99%
CSNpharm
C-82
25mg
| ≥99%
CSNpharm
C-82
10mg
| ≥99%
CSNpharm
C-82
5mg
| ≥99%
CSNpharm
C527
100mg
| ≥95%
CSNpharm
C527
50mg
| ≥95%
CSNpharm
C527
5mg
| ≥95%
CSNpharm
C527
10mg
| ≥95%
CSNpharm
C527
25mg
| ≥95%
CSNpharm
CSNpharm
Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel exerts its effects by inhibiting microtubule growth and assembly, processes that are essential for cells to divide and grow.
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CSNpharm
Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel exerts its effects by inhibiting microtubule growth and assembly, processes that are essential for cells to divide and grow.
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CSNpharm
Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel exerts its effects by inhibiting microtubule growth and assembly, processes that are essential for cells to divide and grow.
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CSNpharm
Cabazitaxel is a semi-synthetic derivative of the natural taxoid 10-deacetylbaccatin III with potential antineoplastic activity. Cabazitaxel exerts its effects by inhibiting microtubule growth and assembly, processes that are essential for cells to divide and grow.
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CSNpharm
Cabralealactone, a natural product isolated and purified from the herbs of Aglaia lawii, is exclusively cytotoxic to NCI-H187 cell line, displayes minimum inhibitory concentration in the range of 25-50 µg mL(-1).
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CSNpharm
Cabralealactone, a natural product isolated and purified from the herbs of Aglaia lawii, is exclusively cytotoxic to NCI-H187 cell line, displayes minimum inhibitory concentration in the range of 25-50 µg mL(-1).
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CSNpharm
CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metalloproteinase-13, vascular endothelial growth factor and glucose transporter-1, but upregulated RUNX2 expression by increasing RUNX2 stability. CADD522 may represent a potential antitumor drug.
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CSNpharm
CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metalloproteinase-13, vascular endothelial growth factor and glucose transporter-1, but upregulated RUNX2 expression by increasing RUNX2 stability. CADD522 may represent a potential antitumor drug.
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CSNpharm
CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metalloproteinase-13, vascular endothelial growth factor and glucose transporter-1, but upregulated RUNX2 expression by increasing RUNX2 stability. CADD522 may represent a potential antitumor drug.
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CSNpharm
CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metalloproteinase-13, vascular endothelial growth factor and glucose transporter-1, but upregulated RUNX2 expression by increasing RUNX2 stability. CADD522 may represent a potential antitumor drug.
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CSNpharm
CADD522 is a small molecule that inhibits the DNA binding of RUNX2. It negatively regulated transcription of RUNX2 target genes such as matrix metalloproteinase-13, vascular endothelial growth factor and glucose transporter-1, but upregulated RUNX2 expression by increasing RUNX2 stability. CADD522 may represent a potential antitumor drug.
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CSNpharm
CSNpharm
Caerulomycin A is a rare and unusual antibiotic containing a core 2, 2′-bispyridyl with an oxime substituent, isolated and purified from a strain of Streptomyces caeruleus.
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CSNpharm
Caerulomycin A is a rare and unusual antibiotic containing a core 2, 2′-bispyridyl with an oxime substituent, isolated and purified from a strain of Streptomyces caeruleus.
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CSNpharm
Caerulomycin A is a rare and unusual antibiotic containing a core 2, 2′-bispyridyl with an oxime substituent, isolated and purified from a strain of Streptomyces caeruleus.
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CSNpharm
Caffeic acid is a hydroxycinnamic acid, a naturally occurring organic compound isolated and purified from the herb of Boehmeria siamensis Craib., with antioxidant, antineoplastic, anti-HIV, choleretic, hepatotropic, and is a strong inhibitor of neutrophil elastase.
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CSNpharm
Caffeic acid phenethyl ester, a natural product isolated and purified from the barks of Cinnamomum cassia Presl, is a potent and specific inhibitor of NF-κB activation, and also displays antioxidant, immunomodulatory and antiinflammatory activities.
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CSNpharm
Caffeic acid phenethyl ester, a natural product isolated and purified from the barks of Cinnamomum cassia Presl, is a potent and specific inhibitor of NF-κB activation, and also displays antioxidant, immunomodulatory and antiinflammatory activities.
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CSNpharm
Caffeic acid phenethyl ester, a natural product isolated and purified from the barks of Cinnamomum cassia Presl, is a potent and specific inhibitor of NF-κB activation, and also displays antioxidant, immunomodulatory and antiinflammatory activities.
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CSNpharm
Caftaric acid, a natural product isolated and purified from the herbs of Echinacea purpurea with anti-mutagenicity, is also an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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CSNpharm
Caftaric acid, a natural product isolated and purified from the herbs of Echinacea purpurea with anti-mutagenicity, is also an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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CSNpharm
Caftaric acid, a natural product isolated and purified from the herbs of Echinacea purpurea with anti-mutagenicity, is also an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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CSNpharm
Caftaric acid, a natural product isolated and purified from the herbs of Echinacea purpurea with anti-mutagenicity, is also an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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CSNpharm
Caftaric acid, a natural product isolated and purified from the herbs of Echinacea purpurea with anti-mutagenicity, is also an inhibitor of the protein-protein interactions mediated by the Src-family kinases.
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CSNpharm
Cajanin, a natural product isolated and purified from the herbs of Kadsura interior, can increase bone mineral density (BMD) at all skeletal sites studied, bone biomechanical strength, mineral apposition rate (MAR) and bone formation rate (BFR), and has strong mitogenic as well as differentiation-promoting effects on osteoblasts that involved subsequent activation of MEK-Erk and Akt […]
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CSNpharm
Cajanin, a natural product isolated and purified from the herbs of Kadsura interior, can increase bone mineral density (BMD) at all skeletal sites studied, bone biomechanical strength, mineral apposition rate (MAR) and bone formation rate (BFR), and has strong mitogenic as well as differentiation-promoting effects on osteoblasts that involved subsequent activation of MEK-Erk and Akt […]
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Calcein
100mg
| Purity Not Available
CSNpharm
CSNpharm
Calcein blue is a short-term and membrane-impermeant fluorescent dye for labeling live cells with excitation and emission maxima of 360, 445 nm respectively).
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