Paclitaxel (Taxol) |
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A4393-100 | ApexBio | 100 mg | EUR 170.4 |
Description: Paclitaxel is a novel antineoplastic agent, which was discovered in a screen of extracts of thousands of plants and natural products for antineoplastic activity by a National Cancer Institute program |
Apexbio Reagents Laboratories manufactures the apexbio paclitaxel reagents distributed by Genprice. The Apexbio Paclitaxel reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact Apexbio Reagents. Other Apexbio products are available in stock. Specificity: Apexbio Category: Paclitaxel
CX-5461 |
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A8337-S | ApexBio | Evaluation Sample | EUR 97.2 |
Description: CX-5461 is a potent and orally bioavailable small-molecule inhibitor of rRNA synthesis that specifically inhibits RNA polymerase (Pol) I-driven transcription with IC50 value of 142 nM. |
NSC 74859 |
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A8338-10 | ApexBio | 10 mg | EUR 157.2 |
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M. |
NSC 74859 |
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A8338-200 | ApexBio | 200 mg | EUR 793.2 |
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M. |
NSC 74859 |
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A8338-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 135.6 |
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M. |
NSC 74859 |
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A8338-50 | ApexBio | 50 mg | EUR 304.8 |
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M. |
NSC 74859 |
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A8338-S | ApexBio | Evaluation Sample | EUR 97.2 |
Description: S3I-201 is a selective inhibitor of Stat3 with IC50 value of 86 ?M [1].In the in vitro Stat3 DNA-binding assay, S3I-201 showed potent inhibition of the Stat3 DNA-binding activity with an average IC50 of 86 ?M. |
TAK-875 |
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A8339-10 | ApexBio | 10 mg | EUR 366 |
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids. |
TAK-875 |
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A8339-5 | ApexBio | 5 mg | EUR 226.8 |
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids. |
TAK-875 |
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A8339-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 268.8 |
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids. |
TAK-875 |
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A8339-50 | ApexBio | 50 mg | EUR 714 |
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids. |
TAK-875 |
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A8339-S | ApexBio | Evaluation Sample | EUR 97.2 |
Description: TAK-875 is a potent, selective, and oral GPR40 agonist. GPR40 is one of the G protein-coupled receptors predominantly expressed in pancreatic ?-cells, mediating enhancement of glucose-stimulated insulin secretion by free fatty acids. |
Cyclopamine |
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A8340-10 | ApexBio | 10 mg | EUR 150 |
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1]. |
Cyclopamine |
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A8340-25 | ApexBio | 25 mg | EUR 199.2 |
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1]. |
Cyclopamine |
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A8340-5 | ApexBio | 5 mg | EUR 129.6 |
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1]. |
Cyclopamine |
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A8340-5.1 | ApexBio | 10 mM (in 1mL DMSO) | EUR 135.6 |
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1]. |
Cyclopamine |
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A8340-S | ApexBio | Evaluation Sample | EUR 97.2 |
Description: Cyclopamine is a naturally occurring Hedgehog (Hh)?specific small?molecule signaling steroidal alkaloid inhibitor, causes a profound inhibition of tumor growth, has significant anti?invasive, anti?proliferative and anti?estrogenic potency in human breast cancer cells [2] [1]. |
Go 6976 |
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A8341-1 | ApexBio | 1 mg | EUR 172.8 |
Description: Go 6976 is a selective inhibitor of PKC with IC50 value of 20 nM [1] [2]. |