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Scutellarin is cytotoxic to cancer cells and could induce DNA damage, metabolic suppression and mitochondrial reactive oxygen species. It has has antioxidant, anti-inflammatory, and antiproliferative biological activities that can be can be found in scutellaria lateriflora.
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CSNpharm
Scutellarin is cytotoxic to cancer cells and could induce DNA damage, metabolic suppression and mitochondrial reactive oxygen species. It has has antioxidant, anti-inflammatory, and antiproliferative biological activities that can be can be found in scutellaria lateriflora.
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CSNpharm
Scutellarin is cytotoxic to cancer cells and could induce DNA damage, metabolic suppression and mitochondrial reactive oxygen species. It has has antioxidant, anti-inflammatory, and antiproliferative biological activities that can be can be found in scutellaria lateriflora.
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CSNpharm
Scutellarin is cytotoxic to cancer cells and could induce DNA damage, metabolic suppression and mitochondrial reactive oxygen species. It has has antioxidant, anti-inflammatory, and antiproliferative biological activities that can be can be found in scutellaria lateriflora.
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CSNpharm
Scutellarin is cytotoxic to cancer cells and could induce DNA damage, metabolic suppression and mitochondrial reactive oxygen species. It has has antioxidant, anti-inflammatory, and antiproliferative biological activities that can be can be found in scutellaria lateriflora.
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CSNpharm
Scutellarin is an active flavonoid that shows anti-tumor activity and anti-proteasome action. It can be isolated from the root of Scutellaria baicalensis Georgi.
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CSNpharm
Scutellarin is an active flavonoid that shows anti-tumor activity and anti-proteasome action. It can be isolated from the root of Scutellaria baicalensis Georgi.
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CSNpharm
Scutellarin is an active flavonoid that shows anti-tumor activity and anti-proteasome action. It can be isolated from the root of Scutellaria baicalensis Georgi.
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CSNpharm
Scutellarin is an active flavonoid that shows anti-tumor activity and anti-proteasome action. It can be isolated from the root of Scutellaria baicalensis Georgi.
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SD-06
1mg
| ≥98%
CSNpharm
SD-06 is a p38 MAP kinase inhibitor and inhibits p38α with an IC50 value of 170 nM and inhibits LPS-stimulated TNF-release in rats(83% inhibition at 1mg/kg, po).
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SD-06
5mg
| ≥98%
CSNpharm
SD-06 is a p38 MAP kinase inhibitor and inhibits p38α with an IC50 value of 170 nM and inhibits LPS-stimulated TNF-release in rats(83% inhibition at 1mg/kg, po).
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SD-06
10mg
| ≥98%
CSNpharm
SD-06 is a p38 MAP kinase inhibitor and inhibits p38α with an IC50 value of 170 nM and inhibits LPS-stimulated TNF-release in rats(83% inhibition at 1mg/kg, po).
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SD-169
100mg
| ≥97%
CSNpharm
SD-169 is an orally active ATP-competitive inhibitor of p38α MAPK, with an IC50 of 3.2 nM. SD-169 also weakly inhibits p38β MAPK with an IC50 of 122 nM. SD-169 prevents the development and progression of diabetes by inhibiting T cell infiltration and activation.
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CSNpharm
SD-169 is an orally active ATP-competitive inhibitor of p38α MAPK, with an IC50 of 3.2 nM. SD-169 also weakly inhibits p38β MAPK with an IC50 of 122 nM. SD-169 prevents the development and progression of diabetes by inhibiting T cell infiltration and activation.
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SDMA
100mg
| ≥98%
CSNpharm
SDMA
25mg
| ≥98%
CSNpharm
SDMA
10mg
| ≥98%
CSNpharm
SDMA
50mg
| ≥98%
CSNpharm
CSNpharm
SEA0400 is a selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
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CSNpharm
SEA0400 is a selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
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CSNpharm
SEA0400 is a selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
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CSNpharm
SEA0400 is a selective inhibitor of the Na+-Ca2+ exchanger with IC50 of 5-33 nM (inhibiting Na+-dependent Ca2+ uptake in cultured neurons, astrocytes, and microglia).
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CSNpharm
Sec-O-glucosylhamaudol is one of the active ingredients isolated and purified from the herb of Ledebouriella seseloides.
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CSNpharm
Sec-O-glucosylhamaudol is one of the active ingredients isolated and purified from the herb of Ledebouriella seseloides.
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CSNpharm
Sec-O-glucosylhamaudol is one of the active ingredients isolated and purified from the herb of Ledebouriella seseloides.
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CSNpharm
Sec-O-glucosylhamaudol is one of the active ingredients isolated and purified from the herb of Ledebouriella seseloides.
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Secoisolariciresinol, a natural product isolated and purified from the Heartwood of Podocarpus spicata, exerts a suppressive effect on the gain of body weight of mice fed a high-fat diet by inducing gene expression of adiponectin, resulting in the altered expression of various genes related to the synthesis and β-oxidation of fatty acids.
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Secoisolariciresinol diglucoside is an antagonist of platelet activating factor-receptor and used as an antioxidant.
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CSNpharm
Secoisolariciresinol diglucoside is an antagonist of platelet activating factor-receptor and used as an antioxidant.
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CSNpharm
Secoisolariciresinol diglucoside is an antagonist of platelet activating factor-receptor and used as an antioxidant.
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CSNpharm
Secoisolariciresinol diglucoside is an antagonist of platelet activating factor-receptor and used as an antioxidant.
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CSNpharm
Secoisolariciresinol diglucoside is an antagonist of platelet activating factor-receptor and used as an antioxidant.
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CSNpharm
Secoisolariciresinol monoglucoside is a natural product isolated and purified from Linum usitatissimum L. cv AC McDuff.
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Secoisolariciresinol monoglucoside is a natural product isolated and purified from Linum usitatissimum L. cv AC McDuff.
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Secoxyloganin, a natural product isolated and purified from the vines of Lonicera japonica, is active against melanoma (UACC-62) cell line.
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Secoxyloganin, a natural product isolated and purified from the vines of Lonicera japonica, is active against melanoma (UACC-62) cell line.
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Secoxyloganin, a natural product isolated and purified from the vines of Lonicera japonica, is active against melanoma (UACC-62) cell line.
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