(Q78287529)

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

title

Cordylactam, a new alkaloid from the spider pathogenic fungus Cordyceps sp. BCC 12671 (English)

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

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cyclo[D-OVal-N(Me)Phe-D-OVal-N(Me)Phe-OVal-N(Me)Phe]

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(2E,10E)-N-[(2R,3S,4aS,8R,8aS)-2,4a-dihydroxy-8-methoxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodeca-2,10-dienamide

1 reference

1 reference

(2E,10E)-N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]-12-hydroxydodeca-2,10-dienamide

1 reference

N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodeca-2,10-dienamide

1 reference

N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]-12-hydroxydodeca-2,10-dienamide

1 reference

(2E,10E)-N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodeca-2,10-dienamide

1 reference

(E)-N-[(1S,2S,4S,5S,6S,7R,8S)-1,7-dihydroxy-5-methoxy-10-oxo-3-oxatricyclo[4.3.1.02,4]decan-8-yl]dodec-2-enamide

1 reference

N-[(2R,3S,4aS,8R,8aS)-2,4a-dihydroxy-8-methoxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodeca-2,10-dienamide

1 reference

N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodec-2-enamide

1 reference

N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]-12-hydroxydodec-2-enamide

1 reference

(E)-N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]-12-hydroxydodec-2-enamide

1 reference

N-[(1S,2S,4S,5S,6S,7R,8S)-1,7-dihydroxy-5-methoxy-10-oxo-3-oxatricyclo[4.3.1.02,4]decan-8-yl]dodec-2-enamide

1 reference

(E)-N-[(2R,3S,4aS,8R,8aR)-8-chloro-2,4a-dihydroxy-8a-methyl-5-oxo-2,3,4,8-tetrahydrochromen-3-yl]dodec-2-enamide

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Janet Jennifer Divinagracia Luangsa-ard

author

5

object named as

J. Jennifer Luangsa-ard

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

6

Nigel L. Hywel-Jones

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

author name string

Masahiko Isaka

1

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

Panida Chinthanom

2

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

Pranee Rachtawee

3

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

Wiwat Somyong

4

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

publication date

20 January 2013

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

number of pages

3

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based on heuristic

inferred from page(s)

published in

Phytochemistry Letters

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

volume

6

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

page(s)

162-164

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https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

issue

2

1 reference

https://api.crossref.org/v1/works/http://dx.doi.org/10.1016/j.phytol.2012.12.009

13 December 2019

Identifiers

1 reference