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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4104 | Ophiopojaponin C | Ophiopogonin C | Others |
Ophiopogonin C' pharmacological activities may be related to the substances in nucleus mainly. | |||
T19971 | Cyclosporin C | CsC,Cs-C,Cyclosporin-C | Antiviral , Antifungal |
Cyclosporin C (Cs-C) is a fungal metabolite against filamentous phytopathogenic fungi. Cyclosporin C has antifungal, antiviral, and immunosuppressant properties. | |||
T34262 | RAPTA-C | Apoptosis | |
RAPTA-C induces EAC cell cycle arrest and apoptosis via the mitochondrial and p53-JNK pathways, and can be used in the study of breast and ovarian cancer. | |||
T19224 | C-Phycocyanin | C-PC | Others |
C-Phycocyanin (C-PC) is a water-soluble protein pigment that is also used as a nutrient supplement for human beings. | |||
T5S1598 | Mulberroside C | Antioxidant , HCV Protease | |
1. Mulberroside C has antioxidant activity. | |||
T4S1615 | Sanggenon C | Sanggenone C | NF-κB |
1. Sanggenon C (Sanggenone C) inhibits tumor cellular proteasomal activity and cell viability, via induction of cell cycle arrest and cell death , inhibiting the proteasome function. 2. Sanggenon C and O inhibited NO pro... | |||
T3397 | Epmedin C | Baohuoside-VI,Epimedin C | Others |
Epmedin C (Baohuoside-VI) was metabolized via desugarization, dehydrogenation, hydrogenation, dehydroxylation, hydroxylation, demethylation and glucuronidation pathways in vivo. It has potential activity against osteopor... | |||
T2S0473 | Rehmannioside C | Others | |
Rehmannioside C is an iridoid glucoside. Rehmannioside C has been isolated from Radix Rehmanniae Praeparata[1]. | |||
TN5118 | Taxol C | P-gp | |
Taxol C can reduce interaction with the P-glycoprotein transporter that may allow for increased permeation of taxanes into the brain. | |||
TN1054 | Loureirin C | Others | |
Loureirin C can inhibit the activities of thrombin in vitro effectively. | |||
T10641 | C-82 | Epigenetic Reader Domain , Wnt/beta-catenin | |
C-82 is a specific CBP/β-catenin antagonist. It inhibits the binding between β-catenin and CBP and increases the binding between β-catenin and p300. | |||
T3106 | C-DIM12 | Apoptosis , Others | |
C-DIM12 induced expression of Nurr1-regulated genes. C-DIM12 increased expression of transfected human Nurr1, induced Nurr1 protein expression in primary dopaminergic neurons and enhanced neuronal survival from exposure ... | |||
T9782 | Cytochrome C | Others | |
Cytochrome C, a protein that belongs to class 1 of the c-type cytochrome family, exerts different functions depending on its cellular localization and the conditions in which it operates. | |||
T3370 | Hederacoside C | Kalopanaxsaponin B,Hederasaponin C | Others , Antibacterial |
Hederacoside C (Hederasaponin C) is expectorant for Cold and cough relief, Bronchitis. | |||
T2S0967 | Sennoside C | Others | |
Sennoside C is an anthraquinone glycoside extracted from leaves and pods of Senna and has an auxiliary effect on the laxative effect of mice. | |||
TMA1603 | Parishin C | Antioxidant | |
Parishin C is a phenolic glycoside and a major component of G. elata, have antioxidant property | |||
T3903 | Angoroside C | Prostaglandin Receptor | |
Angoroside C is a Potential anti-inflammatory compound. Inhibitor of prostaglandin E2 release in mouse peritoneal macrophages in vitro. Shows potent antioxidative activity in reducing the oxidized OH adducts of dAMP and ... | |||
TN1861 | Licoflavone C | 4',5,7-Trihydroxy-8-prenylflavone | Antioxidant , Antifungal |
Licoflavone C (4',5,7-Trihydroxy-8-prenylflavone) is an isoprenoid-based flavonoid compound isolated from the roots of Glycyrrhiza inflata, which possesses antioxidant and antifungal activities, and is known to have a pr... | |||
T2S2211 | Tenuifoliside C | Dehydrogenase | |
Tenuifoliside C, isolated from polygala tenuifolia willd, is a target lactate dehydrogenase inhibitor. It significantly inhibits chlorzoxazone 6-hydroxylation catalyzed by CYP2E1[1]. | |||
T13589 | Caesappanin C | Others | |
Caesappanin C, extracted from the heartwood of Indonesian Caesalpinia sappan L., shows strong proliferation stimulating activity against the primary osteoblastic cells in vitro. |