| 000 | 01804nam a2200301Ia 4500 | ||
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| 003 | MX-MdCICY | ||
| 005 | 20250625160227.0 | ||
| 040 | _cCICY | ||
| 090 | _aB-18309 | ||
| 245 | 1 | 0 | _aA pair of epimeric cassane-type diterpenoids and a new labdane-type derivative from Caesalpinia decapetala. |
| 490 | 0 | _vTetrahedron, 74(28), p.3852-3857, 2018 | |
| 520 | 3 | _aCaesaldecins A and B (1a/1b), a pair of epimeric cassane-type diterpenoids containing an ether linkage between C-6 and C-20 and an ?,?-butenolide ring in the northern hemisphere, were isolated from the leaves of the medicinal plant Caesalpinia decapetala (Roth)Alston, along with a new labdane-type diterpenoid, termed as 8(17),11(Z),13(E)-trien-15,18-dioic acid (2). Structures of 1 and 2 were established by extensive spectroscopic analyses, including HRESIMS, 1D and 2D NMR, and electronic circular dichroism (ECD)calculations. The in vitro antibacterial and inhibitory activities against a panel of bacteria and cancer cell lines were evaluated, respectively. Compound 2 displayed moderate antibacterial activity against the methicillin-resistant Staphylococcus aureus subsp. aureus (MRSA)with an MIC50 value of 5.99??g?mL?1. | |
| 650 | 1 | 4 | _aCAESALPINIA DECAPETALA (ROTH)ALSTON |
| 650 | 1 | 4 | _aCASSANE-TYPE FURANODITERPENOID |
| 650 | 1 | 4 | _aMIXTURE OF EPIMERS |
| 650 | 1 | 4 | _aECD CALCULATIONS |
| 650 | 1 | 4 | _aANTIBACTERIAL ACTIVITIES |
| 700 | 1 | 2 | _aQiao, Y. |
| 700 | 1 | 2 | _aLiu, Y. |
| 700 | 1 | 2 | _aDuan, X. |
| 700 | 1 | 2 | _aChen, C. |
| 700 | 1 | 2 | _aLiu, J. |
| 700 | 1 | 2 | _aZhu, H. |
| 700 | 1 | 2 | _aZhang, Y. |
| 856 | 4 | 0 |
_uhttps://drive.google.com/file/d/19OBytp3ur4XjTtIfCEQTqISf0PUqLxwB/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
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