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Syringaldehyde is a polyphenolic compound belonging to the group of flavonoids and is found in different plant species like Manihot esculenta and Magnolia officinalis. Syringaldehyde moderately inhibits COX-2 activity with an IC50 of 3.5 μg/mL. Anti-hyperglycemic and anti-inflammatory activities.
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Syringaresinol-Di-O-Glucoside is a natural product which exhibits an antidiabetic and antioxidative effect on a streptozotocin‑induced mouse model of diabetes.
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Syringic acid, a natural product isolated and purified from the herbs of Michelia spaerantha C.Y.Wu, is an antimitogenic and chemo-sensitizing agent for human colorectal cancer, reduces oxidative stress and neuronal degeneration in treatment of cerebral ischemia and pretreatment of spinal cord ischemia/reperfusion, and exerts its chemotherapeutic and chemo-sensitizing effects through an array of mechanisms including […]
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Syringic acid, a natural product isolated and purified from the herbs of Michelia spaerantha C.Y.Wu, is an antimitogenic and chemo-sensitizing agent for human colorectal cancer, reduces oxidative stress and neuronal degeneration in treatment of cerebral ischemia and pretreatment of spinal cord ischemia/reperfusion, and exerts its chemotherapeutic and chemo-sensitizing effects through an array of mechanisms including […]
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Syringin is a natural product isolated and purified from the fruits of Syringa vulgaris with antitumour,antiproliferative, anti-inflammatory and antinociceptive effects.
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Syringin is a natural product isolated and purified from the fruits of Syringa vulgaris with antitumour,antiproliferative, anti-inflammatory and antinociceptive effects.
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CSNpharm
Syringin is a natural product isolated and purified from the fruits of Syringa vulgaris with antitumour,antiproliferative, anti-inflammatory and antinociceptive effects.
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CSNpharm
Syringin is a natural product isolated and purified from the fruits of Syringa vulgaris with antitumour,antiproliferative, anti-inflammatory and antinociceptive effects.
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SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
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CSNpharm
SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
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CSNpharm
SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
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CSNpharm
SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
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CSNpharm
SZL P1-41 is Skp2 inhibitor, selectively suppresses Skp2 E3 ligase activity, but not activity of other SCF complexes.
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CSNpharm
T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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CSNpharm
T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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CSNpharm
T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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CSNpharm
T-1101 tosylate is a Hec1/Nek2 (Highly expressed in cancer 1 / NIMA-related kinase 2) inhibitor with antitumor activity. T-1101 tosylate is inactive toward normal cells, kinases and hERG.
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T-1105
100mg
| ≥98%
CSNpharm
T-1105, a novel broad-spectrum viral polymerase inhibitor, structural analogue of T-705, inhibits the polymerases of RNA viruses after being converted to ribonucleoside triphosphate (RTP) metabolite. T-1105 has antiviral activity against various RNA viruses, including Zika virus (ZIKV), influenza virus, arenaviruses, bunyaviruses, West Nile virus (WNV), yellow fever virus (YFV), and foot-and-mouth disease virus (FMDV). T-1105 […]
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Tabersonine, a natural product isolated and purified from the root bark of Voacanga africana Stapf, is a precursor for vincristine used in cancer chemotherapy, the biocompatibility and small size essential for permeating the blood-brain barrier make it a potential therapeutic drug candidate for treating AD.
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Tabersonine, a natural product isolated and purified from the root bark of Voacanga africana Stapf, is a precursor for vincristine used in cancer chemotherapy, the biocompatibility and small size essential for permeating the blood-brain barrier make it a potential therapeutic drug candidate for treating AD.
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CSNpharm
Tabersonine, a natural product isolated and purified from the root bark of Voacanga africana Stapf, is a precursor for vincristine used in cancer chemotherapy, the biocompatibility and small size essential for permeating the blood-brain barrier make it a potential therapeutic drug candidate for treating AD.
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Tachioside, a natural product isolated and purified from the barks of Pinus yunnanensis with antioxidant and α-glucosidase inhibitory activities, decreases lipid content in 3T3-L1 adipocytes by inhibiting lipogenesis, shows antiobesity activities., and can inhibit nitric oxide production in lipopolysaccharides-stimulated RAW 264.7 cells with IC50 value of 12.14 μM.
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CSNpharm
Tachioside, a natural product isolated and purified from the barks of Pinus yunnanensis with antioxidant and α-glucosidase inhibitory activities, decreases lipid content in 3T3-L1 adipocytes by inhibiting lipogenesis, shows antiobesity activities., and can inhibit nitric oxide production in lipopolysaccharides-stimulated RAW 264.7 cells with IC50 value of 12.14 μM.
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Tacrolimus is a potent immunosuppressive drug often administered to transplant recipient patients and exhibits a variety of adverse cardiovascular effects. Its mechanism of action involves the formation of a high affinity complex (Ki = 0.2 nM) with FK-506 binding protein 12 (FKBP12).
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