NatID | 1041 |
Nombre Común | NatID_1041 |
Fórmula Molecular | C10H16 |
Tipo Químico | Prenol lipids > Monoterpenoids |
Peso Molecular | 136.125 g/mol |
Otros nombres |
Smiles | C=C/C(C)=C\CC=C(C)C |
Inchi | InChI=1S/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7-8H,1,6H2,2-4H3/b10-8- |
Inchi Key | IHPKGUQCSIINRJ-NTMALXAHSA-N |
Estructura 3D |
clogP | 3.48 |
TPSA | 0.00 |
HBD | 0 |
HBA | 0 |
Enlaces Rotables | 3 |
Anillos aromáticos | 0 |
Átomos pesados | 10 |
Carbociclos Aromáticos | 0 |
Heterociclos Aromáticos | 0 |
Número de NO | 0 |
EID | Fuente | Semisintético? | Confidence level | Referencias |
---|---|---|---|---|
9172 | Aristolochia argentina | No | Very High | Priestap, H. A., van Baren, C. M., Di Leo Lira, P., Coussio, J. D., & Bandoni, A. L. (2003). Volatile constituents of Aristolochia argentina. Phytochemistry, 63(2), 221–225. https://doi.org/10.1016/s0031-9422(02)00751-3 |
9210 | Lippia integrifolia | No | Unknown | del C. Coronel, A., Cerda-García-Rojas, C. M., Joseph-Nathan, P., & Catalán, C. A. N. (2006). Chemical composition, seasonal variation and a new sesquiterpene alcohol from the essential oil ofLippia integrifolia. Flavour and Fragrance Journal, 21(5), 839–847. https://doi.org/10.1002/ffj.1736 |
9592 | Flourensia oolepis | No | Very High | García, M., Gonzalez-Coloma, A., Donadel, O. J., Ardanaz, C. E., Tonn, C. E., & Sosa, M. E. (2007). Insecticidal effects of Flourensia oolepis Blake (Asteraceae) essential oil. Biochemical Systematics and Ecology, 35(4), 181–187. https://doi.org/10.1016/j.bse.2006.10.009 |
Bioassay ID | NPASS ID | Target | Activity type | Activity |
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