464-98-2
464-98-2
Chemical Structure
Pseudotaraxasterol
- CAS No.: 464-98-2
- Formula:C30H50O
- Molecular Weight:426.72
IUPAC Name: (3S,4aR,6aR,6bR,8aS,12S,12aR,12bR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol
InChIKey: NGFFRJBGMSPDMS-ZJJHUPNDSA-N
SMILES: CC1(C)[C@@H](O)CC[C@]2(C)[C@@]3([H])CC[C@]4([H])[C@@]5([H])[C@H](C)C(C)=CC[C@@](C)5CC[C@](C)4[C@@](C)3CC[C@@]12[H]
Biological Activity: Pseudotaraxasterol shows cytotoxic activity against MOLT-4 cells.
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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Pseudotaraxasterol | 97.01% | Pseudotaraxasterol shows cytotoxic activity against MOLT-4 cells. | ||||||||||||||||||||
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Germanicol | 99.0% | Germanicol is a selective antineoplastic agent against human colon cancer cell lines HCT-116 and HT29 . Germanicol induces apoptosis via chromatin condensation and DNA damage. | ||||||||||||||||||||
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Faradiol | Faradiol is a STAT3 inhibitor. Faradiol exerts anti-inflammatory activity by reducing STAT3 phosphorylation in a concentration-dependent manner and inhibiting LPS-induced IL-6 release from human monocytes, while also exhibiting cytotoxicity against leukemia and non-small cell lung cancer cells. Faradiol can be used in research on leukemia, edema, cancer, non-small cell lung cancer, Phorbol 12-myristate 13-acetate (TPA) (HY-18739)-induced inflammation, and skin tumors. | |||||||||||||||||||||
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Heliantriol C | Heliantriol C is a taraxerane-type trihydroxy triterpenoid present in the ray florets of Asteraceae plants. Heliantriol C inhibits TPA (HY-18739)-induced inflammation. Heliantriol C exhibits anticancer activity, and its acetylated derivatives show enhanced cytotoxicity against cancer cells. Heliantriol C can be used in studies related to inflammation and cancers such as leukemia and lung cancer. | |||||||||||||||||||||
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Lupeol (Standard) | 99.89% | Lupeol (Standard) is the analytical standard of Lupeol. This product is intended for research and analytical applications. Lupeol (Clerodol; Monogynol B; Fagarasterol) is an active pentacyclic?triterpenoid, has anti-oxidant, anti-mutagenic, anti-tumor and anti-inflammatory activity. Lupeol is a potent?androgen receptor (AR)?inhibitor and can be used for cancer research, especially prostate cancer of androgen-dependent phenotype (ADPC) and castration resistant phenotype (CRPC). | ||||||||||||||||||||
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Taraxasterol | 99.41% | Taraxasterol is a pentacyclic triterpenoid compound isolated from Taraxacum mongolicum. Taraxasterol is an LXRα activator, with metabolic and anti-inflammatory effects. Taraxasterol may be used in research on immune-inflammatory diseases. | ||||||||||||||||||||
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30-Oxopseudotaraxasterol | 30-Oxopseudotaraxasterol is a natural product. | |||||||||||||||||||||
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Monogynol A | Monogynol A is an AChE/BChE inhibitor found in the aerial parts of Salvia trichoclada Bentham. Monogynol A can be used for the research of alzheimer’s disease. | |||||||||||||||||||||
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Hennadiol | Hennadiol (Lup-20(29)-ene-3β,30-diol) is a product that can be isolated from . | |||||||||||||||||||||
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Arnidiol | 99.91% | Arnidiol is a pentacyclic triterpene isolated from Barleria Longiflora Linn F.. | ||||||||||||||||||||
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α-Amyrin (Standard) | ≥98% | α-Amyrin (Standard) is a pentacyclic triterpenoid compound with oral activity. α-Amyrin (Standard) activates the ERK and GSK-3β signaling pathways. α-Amyrin (Standard) can inhibit cancer cells proliferation and induce apoptosis. α-Amyrin (Standard) shows anti-bacterial and anti-inflammation activity. α-Amyrin (Standard) can reduce blood glucose level. α-Amyrin (Standard) can be used for the researches of cancer, infection, inflammation, metabolic disease and neurological disease, such as breast cancer, Streptococcus oralis infection, skin inflammation and diabetes. | ||||||||||||||||||||
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