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Glaucium fimbrilligerum

Glaucium fimbrilligerum - Unknown — Part: Unknown
Author: Public Domain - WikiMedia

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Table of Contents

Details

Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

Contributors

Collections

Details Top

Internal ID	UUID64401e0ea88dc320566098
Scientific name	Glaucium fimbrilligerum
Authority	Boiss.
First published in	Fl. Orient. 1: 120 (1867)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Dicranostigma fimbrilligerum	(Boiss.) C.H.An	Fl. Xinjiangensis 5: 481 (1999)
Glaucium fimbrilliferum	(Trautv.) B.Fedtsch.	Trudy Imp. S.-Peterburgsk. Bot. Sada 23: 366 (1904)
Glaucium fimbrilligerum var. leiocarpum	Popov	Opred. Rast. Okr. Taschk. 2: 135 1924
Glaucium luteum var. fimbrilliferum	Trautv.	Bull. Soc. Imp. Naturalistes Moscou 33(1): 92 1860
Glaucium persicum	Bunge	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 7: 192 (1847)

Common names Top

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Language	Common/alternative name
Chinese	海罂粟

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Iran

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000703570
Tropicos	24000588
KEW	urn:lsid:ipni.org:names:673164-1
The Plant List	kew-2826355
Open Tree Of Life	5232169
Observations.org	125288
NCBI Taxonomy	1353837
IPNI	673164-1
GBIF	7315048
Elurikkus	587444

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Taxonomically Informed Scoring Enhances Confidence in Natural Products Annotation

Rutz A, Dounoue-Kubo M, Ollivier S, Bisson J, Bagheri M, Saesong T, Ebrahimi SN, Ingkaninan K, Wolfender JL, Allard PM

Front Plant Sci

25-Oct-2019

PMCID:	PMC6824209
doi:	10.3389/fpls.2019.01329
PMID:	31708947

Alkaloids of the Papaveraceae. XLVI. Alkaloids from Glaucium fimbrilligerum BOISS.

L. Slavíková, J. Slavík

Institute of Organic Chemistry & Biochemistry

20-Sep-2012

doi:	10.1135/CCCC19712385

Biochemistry and Occurrence of O-Demethylation in Plant Metabolism

Hagel JM, Facchini PJ

Front Physiol

15-Jul-2010

PMCID:	PMC3059935
doi:	10.3389/fphys.2010.00014
PMID:	21423357

Glaucium alkaloids

I. A. Israilov, S. U. Karimova, M. S. Yunusov

Springer Science and Business Media LLC

10-Jan-2005

doi:	10.1007/BF00570773

Structure of glaufine

S. U. Karimova, I. A. Israilov, M. S. Yunusov, S. Yu. Yunusov

Springer Science and Business Media LLC

06-Jan-2005

doi:	10.1007/BF00937648

Alkaloids of Glaucium fimbrilligerum

A. Kh. Yunusov, I. A. Israilov, M. S. Yunusov

Springer Science and Business Media LLC

10-Dec-2004

doi:	10.1007/BF00564415

Alkaloids ofGlaucium fimbrilligerum

S. U. Karimova, I. A. Israilov, M. S. Yunusov, S. Yu. Yunusov

Springer Science and Business Media LLC

26-Nov-2004

doi:	10.1007/BF00638780

Alkaloids ofGlaucium fimbrilligerum. II

S. U. Karimova, I. A. Israilov, F. Vezhnik, M. S. Yunusov, Yu. Slavik, S. Yu. Yunusov

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00575709

Structures of glaunine and glaunidine

I. A. Israilov, S. U. Karimova, M. S. Yunusov, S. Yu. Yunusov

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00566107

Structure of glaufidine

I. A. Israilov, S. U. Karimova, M. S. Yunusov, S. Yu. Yunusov

Springer Science and Business Media LLC

20-Nov-2004

doi:	10.1007/BF00570877

(+)-Bulbocapnine-beta-N-oxide from glaucium fimbrilligerum.

Shafiee A, Morteza-Semnani K, Amini M

J Nat Prod

01-Dec-1998

doi:	10.1021/NP9801920
PMID:	9868167

Phytochemical Profile Top

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Aporphines
(+-)-Isocorytuberine	6451384	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
(+/-)-Corydine	111119	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC	341.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
(1-acetyloxy-2,10,11-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-4-yl) acetate	74039794	Click to see CC(=O)OC1CN(C2CC3=C(C4=C2C1=CC(=C4OC(=O)C)OC)C(=C(C=C3)OC)OC)C	441.50	unknown	https://doi.org/10.1007/BF00575709
(11R,12S)-17-methoxy-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-18-ol	163194760	Click to see C[N+]1(CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3)[O-]	341.40	unknown	https://doi.org/10.1021/NP9801920
(12S)-17-methoxy-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-18-ol	10569204	Click to see C[N+]1(CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3)[O-]	341.40	unknown	https://doi.org/10.1021/NP9801920
(6aR)-1-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10,11-triol	163095492	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)O)OC)O	313.30	unknown	https://doi.org/10.1007/BF00575709
(6aR)-2,10-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,11-diol	12304091	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709
(6aS)-1-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10,11-triol	163188018	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)O)OC)O	313.30	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
(6aS)-1,10-dimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,11-diol	101289740	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)O)OC)C=C1)O	313.30	unknown	https://doi.org/10.1021/NP9801920
[(4R,6aS)-1-acetyloxy-2,10,11-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-4-yl] acetate	162921008	Click to see CC(=O)OC1CN(C2CC3=C(C4=C2C1=CC(=C4OC(=O)C)OC)C(=C(C=C3)OC)OC)C	441.50	unknown	https://doi.org/10.1007/BF00575709
1-Hydroxy-2,10,11-trimethoxynoraporphine	78172954	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)O)C=C1)OC	327.40	unknown	https://doi.org/10.1007/BF00638780
1-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-2,10,11-triol	163095491	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)O)OC)O	313.30	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
1,2,10-Trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol	48704	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00638780
1,2,11-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-10-ol	74492151	Click to see COC1=C(C2=C3C(CC4=C2C(=C(C=C4)O)OC)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1007/BF00570773
17-Methoxy-11-methyl-11-oxido-3,5-dioxa-11-azoniapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1(20),2(6),7,14(19),15,17-hexaen-18-ol	85188849	Click to see C[N+]1(CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3)[O-]	341.40	unknown	https://doi.org/10.1021/NP9801920
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol	98369	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
2,10,11-trimethoxy-6-methyl-6-oxido-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1-ol	146116230	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)[O-]	357.40	unknown	https://doi.org/10.1007/BF00564415
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	100020	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC	341.40	unknown	https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00575709
3-Hydroxy-4,15,16-trimethoxy-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2(7),3,5,9,11,13,15-octaen-8-one	135795277	Click to see COC1=C(C2=C(C=C1)C(=O)C3=NC=CC4=CC(=C(C2=C43)OC)OC)O	337.30	unknown	https://doi.org/10.1007/BF00566107 https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415
3,4,15-Trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-16-ol	23266907	Click to see CN1CCC2=CC(=C(C3=C4C(=CC1=C23)C=CC(=C4OC)OC)O)OC	339.40	unknown	https://doi.org/10.1007/BF00564415
4,15,16-Trimethoxy-10-azatetracyclo[7.7.1.0^{2,7}.0^{13,17}]heptadeca-1(16),2,4,6,13(17),14-hexaen-3-ol	5320211	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00638780
4H-Dibenzo(de,g)quinoline-1,4-diol, 5,6,6a,7-tetrahydro-2,10,11-trimethoxy-6-methyl-, (4R,6aS)-	156185	Click to see CN1CC(C2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)O	357.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00570877
Bulbocapnine	12441	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3	325.40	unknown	https://doi.org/10.1021/NP9801920
CID 13853621	13853621	Click to see CN1CC(C2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC)O	357.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
CID 91884708	91884708	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O	327.40	unknown	https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00937648 https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415
Corydine	10153	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)OC)O)OC	341.40	unknown	https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
Corytuberine	160500	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709
Corytuberine, pentahydrate	347379	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709
d-Bulbocapnine	9276	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C(=C(C=C5)OC)O)OCO3	325.40	unknown	https://doi.org/10.1021/NP9801920
Hernagine	133556360	Click to see COC1=C(C2=C3C(CC4=C2C(=C(C=C4)O)OC)NCCC3=C1)OC	327.40	unknown	https://doi.org/10.1007/BF00570773
Isoboldine	133323	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC	327.40	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00564415
Isocorytuberine	12310875	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)OC)O)OC	327.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415
Lindcarpine	324086	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)O)OC)C=C1)O	313.30	unknown	https://doi.org/10.1021/NP9801920
Magnoflorine	73337	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C	342.40	unknown	https://doi.org/10.1007/BF00575709
N-Methyllindcarpine	20556269	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)O	327.40	unknown	https://doi.org/10.1007/BF00638780
Norcorydine	179491	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)O)C=C1)OC	327.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415
Norisocorydine	12313549	Click to see COC1=C(C2=C(CC3C4=C2C(=C(C=C4CCN3)OC)OC)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00638780
Thaliporphine	6992288	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC	341.40	unknown	https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00575709
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
(13S)-1,2-dimethoxy-12-methyl-13H-[1,3]benzodioxolo[5,6-c]phenanthridin-13-ol	162904664	Click to see CN1C(C2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5)O	365.40	unknown	https://doi.org/10.1007/BF00575709
(23S)-24-methyl-5,7,18,20-tetraoxa-24-azahexacyclo[11.11.0.02,10.04,8.014,22.017,21]tetracosa-1(13),2,4(8),9,11,14(22),15,17(21)-octaen-23-ol	163010848	Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)O	349.30	unknown	https://doi.org/10.1007/BF00575709
Dihydrosanguinarine	124069	Click to see CN1CC2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6	333.30	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415
Sanguinarine pseudobase	14313843	Click to see CN1C(C2=C(C=CC3=C2OCO3)C4=C1C5=CC6=C(C=C5C=C4)OCO6)O	349.30	unknown	https://doi.org/10.1007/BF00575709
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
Chelidonine	197810	Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6	353.40	unknown	https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00638780
Chelidonine (+)	10147	Click to see CN1CC2=C(C=CC3=C2OCO3)C4C1C5=CC6=C(C=C5CC4O)OCO6	353.40	unknown	https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00638780
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Quaternary benzophenanthridine alkaloids
Chelerythrine	2703	Click to see C[N+]1=C2C(=C3C=CC(=C(C3=C1)OC)OC)C=CC4=CC5=C(C=C42)OCO5	348.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415
Sanguinarium	5154	Click to see C[N+]1=C2C(=C3C=CC4=C(C3=C1)OCO4)C=CC5=CC6=C(C=C52)OCO6	332.30	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(+)-Isocorypalmine	71261649	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC	341.40	unknown	https://doi.org/10.1007/BF00575709
(+/-)-Isocorypalmine	10220	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC	341.40	unknown	https://doi.org/10.1007/BF00575709
(13aR)-3,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol	1152279	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00575709
(13aS)-3-(hydroxymethyl)-10-methoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol	162879760	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)CO)O)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00638780
(13aS)-3-(hydroxymethyl)-9,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol	154620537	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)CO)O)C=C1)OC	341.40	unknown	https://doi.org/10.1007/BF00638780
(S)-Scoulerine	439654	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00564415
(S)-Tetrahydrocolumbamine	440229	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)OC	341.40	unknown	https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00575709
3-(hydroxymethyl)-10-methoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline-2,9-diol	162879759	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)CO)O)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00638780
3-(hydroxymethyl)-9,10-dimethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-2-ol	162951080	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)CO)O)C=C1)OC	341.40	unknown	https://doi.org/10.1007/BF00638780
Columbamine	72310	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC	338.40	unknown	https://doi.org/10.1007/BF00575709
Scoulerine	22955	Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)O)C=C1)O	327.40	unknown	https://doi.org/10.1007/BF00575709
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine	98570	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3	369.40	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415
Protopine	4970	Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3	353.40	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00564415 https://doi.org/10.1021/NP9801920 https://doi.org/10.1007/BF00575709 https://doi.org/10.1135/CCCC19712385
> Benzenoids / Phenanthrenes and derivatives
Salutaridine	5408233	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1021/NP9801920
Sinoacutine	625160	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1021/NP9801920
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides
Ahpatinin G	139589299	Click to see CC(C)CC(=O)NC(C(C)C)C(=O)NC(C(C)C)C(=O)NC(CC1=CC=CC=C1)C(CC(=O)NC(C)C(=O)NC(CC2=CC=CC=C2)C(CC(=O)OC)O)O	767.90	unknown	https://doi.org/10.1007/BF00575709
> Organoheterocyclic compounds / Dibenzazecins
15-Methyl-7,9,19,21-tetraoxa-15-azapentacyclo[15.7.0.04,12.06,10.018,22]tetracosa-1(17),4,6(10),11,18(22),23-hexaene	15765609	Click to see CN1CCC2=CC3=C(C=C2CCC4=C(C1)C5=C(C=C4)OCO5)OCO3	339.40	unknown	https://doi.org/10.1021/NP9801920
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(R)-Reticuline	440586	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1007/BF00575709
(S)-N-Methylcoclaurine	440584	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	https://doi.org/10.1007/BF00638780
N-Methylcoclaurine	2752274	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC	299.40	unknown	https://doi.org/10.1007/BF00564415 https://doi.org/10.1007/BF00638780
Reticulin	10233	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00638780
Reticuline	439653	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1007/BF00638780 https://doi.org/10.1007/BF00575709 https://doi.org/10.1007/BF00564415

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