Karmitoxin

Karmitoxin
Names
IUPAC name
(2E,4E,8E,22E,26S,27R,28S,29R,33R,34R,35R)-1-amino-36-((2R,3S,4R,5S,6R)-6-((5R,6R)-6-((2S,4S,5S,6S)-6-((1R,2R,3E,15E)-1,2-dihydroxyoctadeca-3,15,17-trien-1-yl)-4,5-dihydroxytetrahydro-2H-pyran-2-yl)-1,5,6-trihydroxy-4-methylenehexyl)-3,4,5-trihydroxytetrahydro-2H-pyran-2-yl)-6,12,16,20,24,27,28,29,34,35-decahydroxy-26,33-dimethylhexatriaconta-2,4,8,22-tetraen-14-one
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C73H127NO23/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-23-36-56(82)66(90)73-67(91)59(85)45-60(97-73)68(92)63(87)47(3)38-39-57(83)72-71(95)70(94)69(93)61(96-72)44-58(84)62(86)46(2)28-25-37-55(81)65(89)64(88)48(4)41-51(77)34-26-32-50(76)33-27-35-53(79)43-54(80)42-52(78)31-21-18-20-29-49(75)30-22-19-24-40-74/h5-7,18-20,22-24,26,30,34,36,46,48-53,55-73,75-79,81-95H,1,3,8-17,21,25,27-29,31-33,35,37-45,74H2,2,4H3/b7-6+,20-18+,24-19+,30-22+,34-26+,36-23+/t46-,48+,49?,50?,51?,52?,53?,55-,56-,57?,58-,59+,60+,61-,62-,63-,64-,65+,66-,67+,68+,69-,70-,71+,72-,73-/m1/s1
    Key: OWONYFGWIVVTML-QNVGQBNPSA-N
  • NC/C=C/C=C/C(C/C=C/CCC(CC(CC(CCCC(C/C=C/C(C[C@@H]([C@@H](O)[C@@H](O)[C@@H](CCC[C@@H](C)[C@@H](O)[C@@H](C[C@]1([H])[C@@H](O)[C@@H](O)[C@H](O)[C@](C(CCC([C@H]([C@H]([C@]2([H])C[C@H](O)[C@H](O)[C@@]([H])([C@H](O)[C@@H](/C=C/CCCCCCCCCC/C=C/C=C)O)O2)O)O)=C)O)([H])O1)O)O)C)O)O)O)=O)O)O
Properties
C73H127NO23
Molar mass 1386.803 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Karmitoxin is an amine-containing polyhydroxy-polyene toxin isolated from Karlodinium armiger strain K-0668.[1] It is structurally related to amphidinols, luteophanols, lingshuiols, carteraols, and karlotoxins.[2]

See also

References

  1. ^ Rasmussen, Silas Anselm; Binzer, Sofie Bjørnholt; Hoeck, Casper; Meier, Sebastian; de Medeiros, Livia Soman; Andersen, Nikolaj Gedsted; Place, Allen; Nielsen, Kristian Fog; Hansen, Per Juel; Larsen, Thomas Ostenfeld (5 April 2017). "Karmitoxin: An Amine-Containing Polyhydroxy-Polyene Toxin from the Marine Dinoflagellate Karlodinium armiger". Journal of Natural Products. 80 (5). American Chemical Society (ACS): 1287–1293. doi:10.1021/acs.jnatprod.6b00860. ISSN 0163-3864. PMC 6446557. PMID 28379705.
  2. ^ Studies in Natural Products Chemistry: Bioactive Natural Products. ISSN. Elsevier Science. 2020. p. 158. ISBN 978-0-12-817906-2. Retrieved 1 October 2024. ... is a macrolide isolated in 2016 from the dinoflagellate Karlodinium armiger. Its structure is related to those of the amphidinols and karlotoxins.


Stub icon

This article about an amine is a stub. You can help Wikipedia by adding missing information.

Content Disclaimer

Informasi ini disarikan dari Wikipedia dan disajikan kembali untuk tujuan edukasi. Konten tersedia di bawah lisensi CC BY-SA 3.0. Kami tidak bertanggung jawab atas ketidakakuratan data yang bersumber dari kontribusi publik tersebut.

  1. The information displayed on this website is sourced in part or in whole from Wikipedia and has been adapted for the purpose of restating it. We strive to provide accurate and relevant information, however:
  2. There is no guarantee of absolute accuracy. Wikipedia is an open, collaborative project that can be edited by anyone, so information is subject to change.
  3. It is not intended to constitute professional advice. The content displayed is for informational and educational purposes only. For important decisions (e.g., medical, legal, or financial), please consult a professional.
  4. Content copyright. Wikipedia is licensed under the Creative Commons Attribution-ShareAlike License (CC BY-SA). This means that content may be reused with appropriate attribution and shared under a similar license.
  5. Responsible use. Any risk arising from the use of information from this website is entirely the responsibility of the user.