| Weight | 426.729 g/mol |
|---|---|
| Formula | C30H50O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Cycloartenol (469-38-5)
Score:
#2947 in Biochemistry
,
#7212 in Chemistry
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- Isolation of an Arabidopsis thaliana gene encoding cycloartenol synthase by functional expression in a yeast mutant lacking lanosterol synthase by the use of a chromatographic screen (Proceedings of the National Academy of Sciences of the United States of America, 1993)
- Inhibitory Effect of Cycloartenol Ferulate, a Component of Rice Bran, on Tumor Promotion in Two-Stage Carcinogenesis in Mouse Skin (Biological & Pharmaceutical Bulletin, 1998)
- Dual biosynthetic pathways to phytosterol via cycloartenol and lanosterol in Arabidopsis (Proceedings of the National Academy of Sciences of the United States of America, 2009)
- Directed Evolution To Investigate Steric Control of Enzymatic Oxidosqualene Cyclization. An Isoleucine-to-Valine Mutation in Cycloartenol Synthase Allows Lanosterol and Parkeol Biosynthesis (Journal of the American Chemical Society, 1999)
- Constituents of cimicifugae rhizoma II. Isolation and structures of new cycloartenol triterpenoids and related compounds from Cimicifuga foetida L (Tetrahedron, 1995)
- Allelic mutant series reveal distinct functions for Arabidopsis cycloartenol synthase 1 in cell viability and plastid biogenesis (Proceedings of the National Academy of Sciences of the United States of America, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C
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InChIKeyONQRKEUAIJMULO-UHFFFAOYSA-N
- Pubchem - Cycloartenol
- Wikipedia - cycloartenol
Cycloartenol is an important triterpenoid of the sterol class which is found in plants. It is the starting point for the synthesis of almost all plant steroids, making them chemically distinct from the steroids of fungi and animals which are instead produced from lanosterol.
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