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| − | '''Kaurane''' is a [[parent | + | {{Multiple image |
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| + | | image1 = kaurane IUPAC.png | ||
| + | | caption1 = IUPAC | ||
| + | | image2 = kaurane CAS.png | ||
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| + | | footer = The two different structures referred to as '''kaurane'''. | ||
| + | }} | ||
| + | '''Kaurane''' is a defined [[fundamental parent structure]] used in the [[IUPAC]] [[nomenclature of natural products]] and also, distinctly, in [[CAS nomenclature]]. It is a [[diterpene]] with a rigid four-ring structure and six [[Chirality|chiral centres]]. | ||
| − | The stereochemistry of the six chiral centres is defined by convention: however, IUPAC and CAS use different | + | ==Ambiguity between IUPAC and CAS== |
| + | [[File:Kaurane numbered.png|thumb|right|217px|The conventional numbering of kaurane: for the numbering of the methyl groups at C-18 and C-19, see text.]] | ||
| + | The stereochemistry of the six chiral centres is defined by convention: however, IUPAC and CAS use different opposite [[enantiomer]]s, which also leads to a slight difference in numbering between the two systems. IUPAC conventional kaurane has (5''S'',8''S'',9''S'',10''S'',13''S'',15''R'')-stereochemistry, and is drawn with the five-membered ring receding into the plane of the image.<ref name="IUPAC">{{IUPAC natural products 1999}}.</ref> CAS conventional kaurane has (5''R'',8''R'',9''R'',10''R'',13''R'',15''S'')-stereochemistry, and is drawn with the five-membered ring protruding from the plane of the image.<ref name="CAS">{{citation | contribution = 57817-89-7 – Kaur-16-en-18-oic acid, 13-[(2-''O''-β-<small>D</small>-glucopyranosyl-β-<small>D</small>-glucopyranosyl)oxy]-, β-<small>D</small>-glucopyranosyl ester, (4α)- | url = http://www.commonchemistry.org/ChemicalDetail.aspx?ref=57817-89-7 | title = Common Chemistry | publisher = Chemical Abstracts Service | accessdate = 2009-09-05}}.</ref> For the two methyl groups attached to carbon-4, the two number systems are identical (but see below): the methyl group receding into the plane of the image is numbered carbon-18 and the one protruding from the plane of the image is numbered carbon-19.<ref name="Errata">{{IUPAC natural products errata 2004}}.</ref><ref group="note">Note that the numbering on the structural diagrams in the appendix to the [http://media.iupac.org/publications/pac/1999/pdf/7104x0587.pdf original version of the IUPAC Recommendations 1999] is [http://media.iupac.org/publications/pac/2004/pdf/7606x1283.pdf ''incorrect''].</ref> | ||
| − | ==References== | + | ===''ent''-Kaurane=== |
| − | {{reflist}} | + | The name ''ent''-kaurane is sometimes used to refer to the CAS conventional kaurane,<ref name="ent">{{citation | first1 = Fumihiro | last1 = Nagashima | first2 = Hironao | last2 = Tanaka | first3 = Shigeru | last3 = Takaoka | first4 = Yoshinori | last4 = Asakawa | title = ''Ent''-kaurane-type diterpenoids from the liverwort ''Jungermannia exsertifolia'' ssp. ''cordifolia'' | journal = Phytochemistry | volume = 41 | issue = 4 | year = 1996 | pages = 1129–41 | doi = 10.1016/0031-9422(95)00755-5}}. {{citation | first1 = Francisco Javier | last1 = Arriaga-Giner | first2 = Angel | last2 = Rumbero | first3 = Eckhard | last3 = Wollenweber | title = 16α,19-Diacetoxy-''ent''-kaurane, a New Natural Diterpene from the Exudate of ''Ozothamnus scutellifolius'' (Asteraceae) | journal = Z. Naturforsch. C | volume = 54 | pages = 602–4 | year = 1999}}. {{citation | title = ''Ent''-kaurane Diterpenoid Glycosides from the Leaves of ''Cussonia racemosa'', a Malagasy Endemic Plant | first1 = Liva Rakotondraibe Romuald | last1 = Harinantenaina | first2 = Ryoji | last2 = Kasai | first3 = Kazuo | last3 = Yamasaki | journal = Chem. Pharm. Bull. | year = 2002 | volume = 50 | issue = 2 | pages = 268–71 | doi = 10.1248/cpb.50.268}}. {{citation | title = Three New Cytotoxic ''ent''-Kaurane Diterpenoids from ''Isodon weisiensis'' C. Y. Wu | first1 = Lan | last1 = Ding | first2 = Zhang-Jing | last2 = Zhang | first3 = Guo-An | last3 = Liu | first4 = Dong-Juan | last4 = Yang | first5 = Guo-Cong | last5 = Guo | first6 = Han | last6 = Wang | first7 = Kun | last7 = Sun | journal = Helv. Chim. Acta | volume = 88 | issue = 9 | year = 2005 | pages = 2502–7 | doi = 10.1002/hlca.200590185}}. {{citation | first1 = Ronan | last1 = Batista | first2 = Pablo A. | last2 = García | first3 = Maria A. | last3 = Castro | first4 = José M. Miguel | last4 = del Corral | first5 = Arturo | last5 = San Feliciano | first6 = Alaíde B. | last6 = de Oliveira | title = New oxidized ''ent''-kaurane and ''ent''-norkaurane derivatives from kaurenoic acid | journal = J. Braz. Chem. Soc. | volume = 18 | issue = 3 | year = 2007 | pages = 622–27 | doi = 10.1590/S0103-50532007000300020}}. {{citation | last1 = Zhao | first1 = Yong | last2 = Pu | first2 = Jian-Xin | last3 = Huang | first3 = Sheng-Xiong | last4 = Ding | first4 = Li-Sheng | last5 = Wu | first5 = Ying-Li | last6 = Li | first6 = Xian | last7 = Yang | first7 = Li-Bin | last8 = Xiao | first8 = Wei-Lie | last9 = Chen | first9 = Guo-Qiang | last10 = Sun | first10 = Han-Dong | title = ''ent''-Kaurane diterpenoids from ''Isodon pharicus'' | journal = J. Nat. Prod. | year = 2009 | volume = 72 | issue = 6 | pages = 988–93 | doi = 10.1021/np9000366 | pmid = 19425589}}.</ref> and so to distinguish it from the IUPAC stereochemistry, in particular by the [[International Union of Biochemistry and Molecular Biology]] (IUBMB).<ref name="EC">{{citation | url = http://www.chem.qmul.ac.uk/iubmb/enzyme/EC4/2/3/19.html | contribution = EC 4.2.3.19 – ''ent''-kaurene synthase | title = IUBMB Enzyme Nomenclature | accessdate = 2009-09-18}}. {{citation | url = http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/14/13/78.html | contribution = EC 1.14.13.78 – ''ent''-kaurene oxidase | title = IUBMB Enzyme Nomenclature | accessdate = 2009-09-05}}. {{citation | url = http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/14/13/79.html | contribution = EC 1.14.13.79 – ''ent''-kaurenoic acid oxidase | title = IUBMB Enzyme Nomenclature | accessdate = 2009-09-05}}.</ref> This is the structure of the cyclic skeleton of all naturally occurring kaurane terpenes. However, the numbering system is distinct between CAS nomenclature and IUBMB nomenclature: the metabolic intermediate [[kaurenoic acid]], which has the (4''S'')-configuration, is kaur-16-en-18-oic acid in CAS nomenclature but ''ent''-kaur-16-en-19-oic acid in IUBMB nomenclature.<ref name="CAS"/><ref name="EC"/><ref group="note">The reason for this difference is that the ''ent'' nomenclature operation reverses the configuration of every chiral centre in the molecule, and so maps C-19 onto C-18 and vice versa. This is clarified in the [http://media.iupac.org/publications/pac/2004/pdf/7606x1283.pdf 2004 errata to the IUPAC Recommendations 1999].</ref> |
| + | |||
| + | ==Occurence== | ||
| + | Kaurane diterpenes have been extracted from a variety of plant species,<ref name="ent"/><ref>{{citation | last1 = Nagashima | first1 = Fumihiro | last2 = Kondoh | first2 = Masuo | last3 = Uematsu | first3 = Toshinari | last4 = Nishiyama | first4 = Akiko | last5 = Saito | first5 = Sayaka | last6 = Sato | first6 = Masao | last7 = Asakawa | first7 = Yoshinori | title = Cytotoxic and apoptosis-inducing ''ent''-kaurane-type diterpenoids from the Japanese liverwort ''Jungermannia truncata'' nees | journal = Chem. Pharm. Bull. | year = 2002 | volume = 50 | issue = 6 | pages = 808–13 | doi = 10.1248/cpb.50.808}}. {{citation | first1 = Maurizio | last1 = Bruno | first2 = Franco | last2 = Piozzi | first3 = Nelly Apostolides | last3 = Arnold | first4 = K. Hüsnü Can | last4 = Başer | first5 = Nurhayat | last5 = Tabanca | first6 = Neşe | last6 = Kirimer | title = Kaurane Diterpenoids from Three ''Sideritis'' Species | url = http://journals.tubitak.gov.tr/chem/issues/kim-05-29-1/kim-29-1-7-0402-1.pdf | journal = Turk. J. Chem. | volume = 29 | issue = 1 | year = 2005 | pages = 61–64}}. {{citation | last1 = Kim | first1 = Ki Hyun | last2 = Choi | first2 = Sang Un | last3 = Lee | first3 = Kang Ro | title = Diterpene glycosides from the seeds of ''Pharbitis nil'' | journal = J. Nat. Prod. | year = 2009 | volume = 72 | issue = 6 | pages = 1121–27 | doi = 10.1021/np900101t | pmid = 19435339}}.</ref> in particular ''Stevia'' sp., the source of the [[steviol glycoside]]s [[stevioside]] and [[rebaudioside-A]] that have been used as [[artificial sweetner]]s.<ref>{{citation | title = An efficient microwave-assisted extraction process of stevioside and rebaudioside-A from ''Stevia rebaudiana'' (Bertoni) | last1 = Jaitak | first1 = Vikas | last2 = Bikram Singh | first2 = Bandna | last3 = Kaul | first3 = V. K. | journal = Phytochem. Anal. | year = 2009 | volume = 20 | issue = 3 | pages = 240–45 | doi = 10.1002/pca.1120 | pmid = 19358287}}.</ref> They are intermediates in [[gibberellin biosynthesis]], leading to a group of important plant hormones ([[gibberellin]]s):<ref>{{citation | last1 = Brandle | first1 = J. E. | last2 = Telmer | first2 = P. G. | title = Steviol glycoside biosynthesis | journal = Phytochemistry | year = 2007 | volume = 68 | issue = 14 | pages = 1855–63 | doi = 10.1016/j.phytochem.2007.02.010}}.</ref> [[Gibberellin A12|gibberellin A<sub>12</sub>]] is [[Biosynthesis|biosynthesized]] from [[Ent-Kaurene|''ent''-kaurene]] by six successive [[oxidation]]s catalyzed by [[Ent-Kaurene oxidase|''ent''-kaurene oxidase]] (EC 1.14.13.78) and [[Ent-Kaurenoic acid oxidase|''ent''-kaurenoic acid oxidase]] (EC 1.14.13.79).<ref name="EC"/> The ''ent''-kaurane skeleton is also found in [[veatchine]] and other ''Garrya'' [[alkaloid]]s.<ref>{{citation | first1 = S. William | last1 = Pelletier | first2 = Naresh V. | last2 = Mody | contribution = The Chemistry of C<sub>20</sub>-Diterpenoid Alkaloids | title = The Alkaloids: Chemistry and Pharmacology | editor1-first = R. H. F. | editor1-last = Manske | editor2-first = R. G. A. | editor2-last = Rodrigo | volume = 18 | year = 1981 | location = New York | publisher = Academic Press | pages = 102–21 | isbn = 0-12-469518-3}}.</ref> | ||
| + | |||
| + | ==Notes and references== | ||
| + | ===Notes=== | ||
| + | {{reflist|group=note}} | ||
| + | |||
| + | ===References=== | ||
| + | {{reflist|2}} | ||
==Further reading== | ==Further reading== | ||
| − | *{{citation | | + | *{{citation | first1 = Jeong-Hyung | last1 = Lee | first2 = Tae Hyeon | last2 = Koo | first3 = Bang Yeon | last3 = Hwang | first4 = Jung Joon | last4 = Lee | title = Kaurane Diterpene, Kamebakaurin, Inhibits NF-κB by Directly Targeting the DNA-binding Activity of p50 and Blocks the Expression of Antiapoptotic NF-κB Target Genes | journal = J. Biol. Chem. | year = 2002 | volume = 277 | issue = 21 | pages = 18411–20 | doi = 10.1074/jbc.M201368200}}. |
| − | *{{citation | | + | *{{citation | first = Satoru | last = Masamune | title = Total Syntheses of Diterpenes and Diterpene Alkaloids. II. A Tetracyclic Common Intermediate | journal = J. Am. Chem. Soc. | year = 1964 | volume = 86 | issue = 2 | pages = 288–89 | doi = 10.1021/ja01056a040}}. |
| − | *{{citation | | + | *{{citation | journal = Nature Chem. Biol. | volume = 3 | pages = 396–407 | year = 2007 | doi = 10.1038/nchembio.2007.1 | title = Modern synthetic efforts toward biologically active terpenes | first1 = Thomas J. | last1 = Maimone | first2 = Phil S. | last2 = Baran}}. |
| + | |||
| + | ==External links== | ||
| + | *[http://chemistry.about.com/od/factsstructures/ig/Chemical-Structures---K/Kaurane.-0xj.htm Kaurane Chemical Structure] (shows the IUPAC conventional structure) | ||
| + | *[http://www.find-health-articles.com/msh-diterpenes-kaurane.htm Diterpenes, Kaurane – Research News and Information] | ||
[[Category:Diterpenes]] | [[Category:Diterpenes]] | ||
| − | [[Category:Nomenclature of | + | [[Category:Kaurane terpenoids|*]] |
| + | [[Category:Nomenclature of terpenes and terpenoids]] | ||
{{CC-BY-3.0}} | {{CC-BY-3.0}} | ||
Latest revision as of 05:40, 11 March 2010
IUPAC
CAS
The two different structures referred to as kaurane.
Kaurane is a defined fundamental parent structure used in the IUPAC nomenclature of natural products and also, distinctly, in CAS nomenclature. It is a diterpene with a rigid four-ring structure and six chiral centres.
Contents
Ambiguity between IUPAC and CAS
The stereochemistry of the six chiral centres is defined by convention: however, IUPAC and CAS use different opposite enantiomers, which also leads to a slight difference in numbering between the two systems. IUPAC conventional kaurane has (5S,8S,9S,10S,13S,15R)-stereochemistry, and is drawn with the five-membered ring receding into the plane of the image.[1] CAS conventional kaurane has (5R,8R,9R,10R,13R,15S)-stereochemistry, and is drawn with the five-membered ring protruding from the plane of the image.[2] For the two methyl groups attached to carbon-4, the two number systems are identical (but see below): the methyl group receding into the plane of the image is numbered carbon-18 and the one protruding from the plane of the image is numbered carbon-19.[3][note 1]
ent-Kaurane
The name ent-kaurane is sometimes used to refer to the CAS conventional kaurane,[4] and so to distinguish it from the IUPAC stereochemistry, in particular by the International Union of Biochemistry and Molecular Biology (IUBMB).[5] This is the structure of the cyclic skeleton of all naturally occurring kaurane terpenes. However, the numbering system is distinct between CAS nomenclature and IUBMB nomenclature: the metabolic intermediate kaurenoic acid, which has the (4S)-configuration, is kaur-16-en-18-oic acid in CAS nomenclature but ent-kaur-16-en-19-oic acid in IUBMB nomenclature.[2][5][note 2]
Occurence
Kaurane diterpenes have been extracted from a variety of plant species,[4][6] in particular Stevia sp., the source of the steviol glycosides stevioside and rebaudioside-A that have been used as artificial sweetners.[7] They are intermediates in gibberellin biosynthesis, leading to a group of important plant hormones (gibberellins):[8] gibberellin A12 is biosynthesized from ent-kaurene by six successive oxidations catalyzed by ent-kaurene oxidase (EC 1.14.13.78) and ent-kaurenoic acid oxidase (EC 1.14.13.79).[5] The ent-kaurane skeleton is also found in veatchine and other Garrya alkaloids.[9]
Notes and references
Notes
- ↑ Note that the numbering on the structural diagrams in the appendix to the original version of the IUPAC Recommendations 1999 is incorrect.
- ↑ The reason for this difference is that the ent nomenclature operation reverses the configuration of every chiral centre in the molecule, and so maps C-19 onto C-18 and vice versa. This is clarified in the 2004 errata to the IUPAC Recommendations 1999.
References
- ↑ Revised Section F: Natural Products and Related Compounds (IUPAC Recommendations 1999). Pure Appl. Chem., 71 (4), 587–643. DOI: 10.1351/pac199971040587.
- ↑ 2.0 2.1 57817-89-7 – Kaur-16-en-18-oic acid, 13-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-, β-D-glucopyranosyl ester, (4α)-. In Common Chemistry; Chemical Abstracts Service, <http://www.commonchemistry.org/ChemicalDetail.aspx?ref=57817-89-7>. (accessed 5 September 2009).
- ↑ Revised Section F: Natural products and related compounds (IUPAC Recommendations 1999). Corrections and modifications (2004). Pure Appl. Chem., 76 (6), 1283–92. DOI: 10.1351/pac200476061283.
- ↑ 4.0 4.1 Nagashima, Fumihiro; Tanaka, Hironao; Takaoka, Shigeru; Asakawa, Yoshinori Ent-kaurane-type diterpenoids from the liverwort Jungermannia exsertifolia ssp. cordifolia. Phytochemistry 1996, 41 (4), 1129–41. DOI: 10.1016/0031-9422(95)00755-5. Arriaga-Giner, Francisco Javier; Rumbero, Angel; Wollenweber, Eckhard 16α,19-Diacetoxy-ent-kaurane, a New Natural Diterpene from the Exudate of Ozothamnus scutellifolius (Asteraceae). Z. Naturforsch. C 1999, 54, 602–4. Harinantenaina, Liva Rakotondraibe Romuald; Kasai, Ryoji; Yamasaki, Kazuo Ent-kaurane Diterpenoid Glycosides from the Leaves of Cussonia racemosa, a Malagasy Endemic Plant. Chem. Pharm. Bull. 2002, 50 (2), 268–71. DOI: 10.1248/cpb.50.268. Ding, Lan; Zhang, Zhang-Jing; Liu, Guo-An; Yang, Dong-Juan; Guo, Guo-Cong; Wang, Han; Sun, Kun Three New Cytotoxic ent-Kaurane Diterpenoids from Isodon weisiensis C. Y. Wu. Helv. Chim. Acta 2005, 88 (9), 2502–7. DOI: 10.1002/hlca.200590185. Batista, Ronan; García, Pablo A.; Castro, Maria A.; del Corral, José M. Miguel; San Feliciano, Arturo; de Oliveira, Alaíde B. New oxidized ent-kaurane and ent-norkaurane derivatives from kaurenoic acid. J. Braz. Chem. Soc. 2007, 18 (3), 622–27. DOI: 10.1590/S0103-50532007000300020. Zhao, Yong; Pu, Jian-Xin; Huang, Sheng-Xiong; Ding, Li-Sheng; Wu, Ying-Li; Li, Xian; Yang, Li-Bin; Xiao, Wei-Lie, et al. ent-Kaurane diterpenoids from Isodon pharicus. J. Nat. Prod. 2009, 72 (6), 988–93. PMID 19425589. DOI: 10.1021/np9000366.
- ↑ 5.0 5.1 5.2 EC 4.2.3.19 – ent-kaurene synthase. In IUBMB Enzyme Nomenclature, <http://www.chem.qmul.ac.uk/iubmb/enzyme/EC4/2/3/19.html>. (accessed 18 September 2009). EC 1.14.13.78 – ent-kaurene oxidase. In IUBMB Enzyme Nomenclature, <http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/14/13/78.html>. (accessed 5 September 2009). EC 1.14.13.79 – ent-kaurenoic acid oxidase. In IUBMB Enzyme Nomenclature, <http://www.chem.qmul.ac.uk/iubmb/enzyme/EC1/14/13/79.html>. (accessed 5 September 2009).
- ↑ Nagashima, Fumihiro; Kondoh, Masuo; Uematsu, Toshinari; Nishiyama, Akiko; Saito, Sayaka; Sato, Masao; Asakawa, Yoshinori Cytotoxic and apoptosis-inducing ent-kaurane-type diterpenoids from the Japanese liverwort Jungermannia truncata nees. Chem. Pharm. Bull. 2002, 50 (6), 808–13. DOI: 10.1248/cpb.50.808. Bruno, Maurizio; Piozzi, Franco; Arnold, Nelly Apostolides; Başer, K. Hüsnü Can; Tabanca, Nurhayat; Kirimer, Neşe Kaurane Diterpenoids from Three Sideritis Species. Turk. J. Chem. 2005, 29 (1), 61–64, <http://journals.tubitak.gov.tr/chem/issues/kim-05-29-1/kim-29-1-7-0402-1.pdf>. Kim, Ki Hyun; Choi, Sang Un; Lee, Kang Ro Diterpene glycosides from the seeds of Pharbitis nil. J. Nat. Prod. 2009, 72 (6), 1121–27. PMID 19435339. DOI: 10.1021/np900101t.
- ↑ Jaitak, Vikas; Bikram Singh, Bandna; Kaul, V. K. An efficient microwave-assisted extraction process of stevioside and rebaudioside-A from Stevia rebaudiana (Bertoni). Phytochem. Anal. 2009, 20 (3), 240–45. PMID 19358287. DOI: 10.1002/pca.1120.
- ↑ Brandle, J. E.; Telmer, P. G. Steviol glycoside biosynthesis. Phytochemistry 2007, 68 (14), 1855–63. DOI: 10.1016/j.phytochem.2007.02.010.
- ↑ Pelletier, S. William; Mody, Naresh V. The Chemistry of C20-Diterpenoid Alkaloids. In The Alkaloids: Chemistry and Pharmacology; Manske, R. H. F.; Rodrigo, R. G. A., Eds.; Academic Press: New York, 1981; Vol. 18, pp 102–21. ISBN 0-12-469518-3.
Further reading
- Lee, Jeong-Hyung; Koo, Tae Hyeon; Hwang, Bang Yeon; Lee, Jung Joon Kaurane Diterpene, Kamebakaurin, Inhibits NF-κB by Directly Targeting the DNA-binding Activity of p50 and Blocks the Expression of Antiapoptotic NF-κB Target Genes. J. Biol. Chem. 2002, 277 (21), 18411–20. DOI: 10.1074/jbc.M201368200.
- Masamune, Satoru Total Syntheses of Diterpenes and Diterpene Alkaloids. II. A Tetracyclic Common Intermediate. J. Am. Chem. Soc. 1964, 86 (2), 288–89. DOI: 10.1021/ja01056a040.
- Maimone, Thomas J.; Baran, Phil S. Modern synthetic efforts toward biologically active terpenes. Nature Chem. Biol. 2007, 3, 396–407. DOI: 10.1038/nchembio.2007.1.
External links
- Kaurane Chemical Structure (shows the IUPAC conventional structure)
- Diterpenes, Kaurane – Research News and Information
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