Database	ID/link to page
World Flora Online	wfo-0001021493
UNII	X3Y4M7SQQ3
USDA Plants	DUMY
Tropicos	29605762
INPN	673611
KEW	urn:lsid:ipni.org:names:815656-1
The Plant List	kew-2778803
PFAF	Duboisia myoporoides
Open Tree Of Life	810421
NCBI Taxonomy	195737
IUCN Red List	146118514
IPNI	815656-1
iNaturalist	538021
GBIF	5341761
Freebase	/m/04jdt5l
EPPO	DUBMY
EOL	486419
USDA GRIN	14734
Wikipedia	Duboisia_myoporoides

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

Strategies, Achievements, and Potential Challenges of Plant and Microbial Chassis in the Biosynthesis of Plant Secondary Metabolites

Han T, Miao G

Molecules

02-May-2024

PMCID:	PMC11085123
doi:	10.3390/molecules29092106
PMID:	38731602

Agrobacterium rhizogenes: paving the road to research and breeding for woody plants

Ying W, Wen G, Xu W, Liu H, Ding W, Zheng L, He Y, Yuan H, Yan D, Cui F, Huang J, Zheng B, Wang X

Front Plant Sci

14-Nov-2023

PMCID:	PMC10682722
doi:	10.3389/fpls.2023.1196561
PMID:	38034586

Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants

Biswas D, Chakraborty A, Mukherjee S, Ghosh B

Front Plant Sci

04-Sep-2023

PMCID:	PMC10507345
doi:	10.3389/fpls.2023.1197555
PMID:	37731987

Metabolic Effects of Elicitors on the Biosynthesis of Tropane Alkaloids in Medicinal Plants

Wen Y, Liao Y, Tang Y, Zhang H, Zhang J, Liao Z

Plants (Basel)

24-Aug-2023

PMCID:	PMC10490125
doi:	10.3390/plants12173050
PMID:	37687296

From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds

Isopencu GO, Covaliu-Mierlă CI, Deleanu IM

Plants (Basel)

16-Jul-2023

PMCID:	PMC10386126
doi:	10.3390/plants12142661
PMID:	37514275

Revealing evolution of tropane alkaloid biosynthesis by analyzing two genomes in the Solanaceae family

Zhang F, Qiu F, Zeng J, Xu Z, Tang Y, Zhao T, Gou Y, Su F, Wang S, Sun X, Xue Z, Wang W, Yang C, Zeng L, Lan X, Chen M, Zhou J, Liao Z

Nat Commun

15-Mar-2023

PMCID:	PMC10017790
doi:	10.1038/s41467-023-37133-4
PMID:	36922496

An efficient Agrobacterium-mediated transient transformation system and its application in gene function elucidation in Paeonia lactiflora Pall

Guan S, Kang X, Ge J, Fei R, Duan S, Sun X

Front Plant Sci

06-Oct-2022

PMCID:	PMC9582852
doi:	10.3389/fpls.2022.999433
PMID:	36275545

Aboriginal medicinal plants of Queensland: ethnopharmacological uses, species diversity, and biodiscovery pathways

Turpin G, Ritmejerytė E, Jamie J, Crayn D, Wangchuk P

J Ethnobiol Ethnomed

10-Aug-2022

PMCID:	PMC9364609
doi:	10.1186/s13002-022-00552-6
PMID:	35948982

The vessel wall thickness–vessel diameter relationship across woody angiosperms

Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME

Am J Bot

12-Jun-2022

PMCID:	PMC9328290
doi:	10.1002/ajb2.1854
PMID:	35435252

Plant Secondary Metabolites Produced in Response to Abiotic Stresses Has Potential Application in Pharmaceutical Product Development

Yeshi K, Crayn D, Ritmejerytė E, Wangchuk P

Molecules

05-Jan-2022

PMCID:	PMC8746929
doi:	10.3390/molecules27010313
PMID:	35011546

Potent Antibacterial Prenylated Acetophenones from the Australian Endemic Plant Acronychia crassipetala

Tran TD, Olsson MA, McMillan DJ, Cullen JK, Parsons PG, Reddell PW, Ogbourne SM

Antibiotics (Basel)

06-Aug-2020

PMCID:	PMC7460405
doi:	10.3390/antibiotics9080487
PMID:	32781771

Interpol review of controlled substances 2016–2019

Jones NS, Comparin JH

Forensic Sci Int Synerg

24-May-2020

PMCID:	PMC7770462
doi:	10.1016/j.fsisyn.2020.01.019
PMID:	33385148

Regioselectivity of hyoscyamine 6β-hydroxylase-catalysed hydroxylation as revealed by high-resolution structural information and QM/MM calculations

Kluza A, Wojdyla Z, Mrugala B, Kurpiewska K, Porebski PJ, Niedzialkowska E, Minor W, Weiss MS, Borowski T

Dalton Trans

07-Apr-2020

PMCID:	PMC9705211
doi:	10.1039/d0dt00302f
PMID:	32182320

Vegetation structure and ground cover attributes describe the occurrence of a newly discovered carnivorous marsupial on the Tweed Shield Volcano caldera, the endangered black‐tailed dusky antechinus (Antechinus arktos)

Riordan CE, Pearce C, McDonald BJ, Gynther I, Baker AM

Ecol Evol

12-Feb-2020

PMCID:	PMC7042678
doi:	10.1002/ece3.6045
PMID:	32128142

Medicinal Plant Analysis: A Historical and Regional Discussion of Emergent Complex Techniques

Fitzgerald M, Heinrich M, Booker A

Front Pharmacol

09-Jan-2020

PMCID:	PMC6962180
doi:	10.3389/fphar.2019.01480
PMID:	31998121

Phytochemical Profile Top

Add a new one!

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
(R)-3-(Piperidin-2-YL)pyridine	641266	Click to see C1CCNC(C1)C2=CN=CC=C2	162.23	unknown	https://doi.org/10.1039/JR9570003967
1-(1-Methylpyrrolidin-2-yl)acetone	94157	Click to see CC(=O)CC1CCCN1C	141.21	unknown	https://doi.org/10.1271/BBB.58.1824
3-Piperidin-2-ylpyridine	2181	Click to see C1CCNC(C1)C2=CN=CC=C2	162.23	unknown	https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1039/JR9570003967 https://doi.org/10.1248/CPB.39.1263
Anabasine	205586	Click to see C1CCNC(C1)C2=CN=CC=C2	162.23	unknown	https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1248/CPB.39.1263
Cuscohygrine	1201543	Click to see CN1CCCC1CC(=O)CC2CCCN2C	224.34	unknown	https://doi.org/10.1271/BBB.58.1824
Cuskhygrine	441070	Click to see CN1CCCC1CC(=O)CC2CCCN2C	224.34	unknown	https://doi.org/10.1271/BBB.58.1824
Hygrine	440933	Click to see CC(=O)CC1CCCN1C	141.21	unknown	https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1271/BBB.58.1824
> Alkaloids and derivatives / Tropane alkaloids
(1R,3S,5R,6RS)-6-Hydroxy-8-methyl-8-azabicyclo(3.2.1)oct-3-YL (2S)-3-hydroxy-2-phenylpropanoate	139033153	Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3	305.40	unknown	https://doi.org/10.1016/0031-9422(91)85120-O
(6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) (2S)-3-hydroxy-2-phenylpropanoate	129628892	Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3	305.40	unknown	https://doi.org/10.1016/0031-9422(92)80490-6 https://doi.org/10.1271/BBB.58.1824
(R)-(-)-Littorine	12311316	Click to see CN1C2CCC1CC(C2)OC(=O)C(CC3=CC=CC=C3)O	289.40	unknown	https://doi.org/10.1007/BF00462871
(S)-((1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate	6931560	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/0031-9422(91)83191-M https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1300/J044V04N03_08 https://doi.org/10.1016/0031-9422(89)80374-7 https://doi.org/10.1271/BBB.58.1443 https://doi.org/10.1016/S0031-9422(00)81107-3 https://doi.org/10.1007/BF00462871 https://doi.org/10.1271/BBB.58.1824
[(1R,5R)-8-methyl-8-azabicyclo[3.2.1]octan-1-yl] propanoate	141478070	Click to see CCC(=O)OC12CCCC(N1C)CC2	197.27	unknown	https://doi.org/10.1271/BBB.58.1824
6-Hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate	2198	Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3	305.40	unknown	https://doi.org/10.1016/0031-9422(92)80490-6
8-Azabicyclo[3.2.1]octan-3-yl 3-methylbutanoate	12314489	Click to see CC(C)CC(=O)OC1CC2CCC(C1)N2	211.30	unknown	https://doi.org/10.1039/JR9380001685
8-Methyl-8-azabicyclo[3.2.1]octan-3-ol	8424	Click to see CN1C2CCC1CC(C2)O	141.21	unknown	https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1055/S-0028-1099896 https://doi.org/10.1055/S-0028-1100007 https://doi.org/10.1016/0031-9422(89)80374-7
8-Methyl-8-azabicyclo[3.2.1]octan-3-yl (2S)-2-methylbutanoate	131637782	Click to see CCC(C)C(=O)OC1CC2CCC(C1)N2C	225.33	unknown	https://doi.org/10.1016/0031-9422(92)80490-6
Anisodamine	6918612	Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3	305.40	unknown	https://doi.org/10.1016/0031-9422(92)80490-6
Apoatropine	64695	Click to see CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3	271.35	unknown	https://doi.org/10.1016/0031-9422(92)80490-6 https://doi.org/10.1271/BBB.58.1824
Atropine	174174	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1016/S0176-1617(11)82043-2 https://doi.org/10.1248/CPB.39.1263
L-Hyoscyamine	3661	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/S0176-1617(11)82043-2 https://doi.org/10.1055/S-0028-1099896 https://doi.org/10.1055/S-0028-1097183 https://doi.org/10.1248/CPB.33.5445
L-Hyoscyamine	64692	Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3	289.40	unknown	https://doi.org/10.1016/0031-9422(91)83191-M https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1300/J044V04N03_08 https://doi.org/10.1016/0031-9422(89)80374-7 https://doi.org/10.1271/BBB.58.1443 https://doi.org/10.1007/BF00462871 https://doi.org/10.1271/BBB.58.1824
Littorine	443005	Click to see CN1C2CCC1CC(C2)OC(=O)C(CC3=CC=CC=C3)O	289.40	unknown	https://doi.org/10.1007/BF00462871
Norhyoscyamine	64696	Click to see C1CC2CC(CC1N2)OC(=O)C(CO)C3=CC=CC=C3	275.34	unknown	https://doi.org/10.1016/0031-9422(91)85120-O
Tropine isobutyrate	3083598	Click to see CC(C)C(=O)OC1CC2CCC(C1)N2C	211.30	unknown	https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1016/0031-9422(92)80490-6
Tropine nonanoate	177828	Click to see CCCCCCCCC(=O)OC1CC2CCC(C1)N2C	281.40	unknown	https://doi.org/10.1016/0031-9422(92)80490-6
Tropinone	79038	Click to see CN1C2CCC1CC(=O)C2	139.19	unknown	https://doi.org/10.1271/BBB.58.1824
Valtropine	12444666	Click to see CCC(C)C(=O)OC1CC2CCC(C1)N2C	225.33	unknown	https://doi.org/10.1055/S-0028-1099896
> Benzenoids / Benzene and substituted derivatives / Anilides / Aromatic anilides / Benzanilides
Cystobactamid 861-2	146684631	Click to see CC(C)OC1=C(C=CC(=C1O)C(=O)NC2=CC=C(C=C2)C(=O)O)NC(=O)C3=CC=C(C=C3)NC(=O)C(C(C(=O)N)OC)NC(=O)C4=CC=C(C=C4)NC(=O)C5=CC=C(C=C5)[N+](=O)[O-]	861.80	unknown	https://doi.org/10.1055/S-0028-1099896
> Benzenoids / Benzene and substituted derivatives / Styrenes
(9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl) 2-phenylprop-2-enoate	4486617	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(=C)C4=CC=CC=C4	285.34	unknown	https://doi.org/10.1055/S-0028-1099896
[(1S,2R,4R,5R)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] 2-phenylprop-2-enoate	98104494	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(=C)C4=CC=CC=C4	285.34	unknown	https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1016/0031-9422(91)85120-O
> Hydrocarbons / Saturated hydrocarbons
6-Methyl-dotriacontane	6431085	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(C)CCCCC	464.90	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
(6R)-6-methyldotriacontane	162981197	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(C)CCCCC	464.90	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Hentriacontyl tetratriacontanoate	86254878	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	943.70	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetratriacontanoic acid	94485	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	508.90	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(25S)-25-hydroxydotriacontan-3-one	162945216	Click to see CCCCCCCC(CCCCCCCCCCCCCCCCCCCCCC(=O)CC)O	480.80	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
(30R)-30-hydroxydotriacontan-5-one	163194795	Click to see CCCCC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC(CC)O	480.80	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
25-Hydroxydotriacontan-3-one	14559838	Click to see CCCCCCCC(CCCCCCCCCCCCCCCCCCCCCC(=O)CC)O	480.80	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
30-Hydroxydotriacontan-5-one	71328788	Click to see CCCCC(=O)CCCCCCCCCCCCCCCCCCCCCCCCC(CC)O	480.80	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
Dotriacontanol	96117	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO	466.90	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4R,4aS,6aR,6bS,8S,8aR,12aS,14aS,14bS)-8a-[(2R,3S,4R,5S)-3-[(2R,3S,4S,5S,6S)-5-acetyloxy-3-hydroxy-6-methyl-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid	162963026	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4O)C)(CCC7C6(CC(C(C7(C)C(=O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)O)O)O)OC9C(C(C(CO9)O)O)O)OC(=O)C	1133.20	unknown	https://doi.org/10.1055/S-0028-1100007 https://doi.org/10.1055/S-0028-1099896
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Oxolup-20(29)-en-28-oic acid	289985	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
beta-Ursolic acid	220774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
Betulonic acid	122844	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)80500-2
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	https://doi.org/10.1021/JF020691D
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	https://doi.org/10.1002/(SICI)1099-1573(199606)10:4<359::AID-PTR841>3.0.CO;2-C https://doi.org/10.1016/S0031-9422(00)80500-2 https://doi.org/10.1021/JF020691D
> Lipids and lipid-like molecules / Saccharolipids / Acyltrehaloses
CID 85149698	85149698	Click to see CCCCCCCCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)O)COC(=O)C)O)O	650.80	unknown	https://doi.org/10.1055/S-0028-1097183 https://doi.org/10.1055/S-0028-1099896
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(E,2R)-N-[(2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadecan-2-yl]-2-hydroxytetracos-4-enamide	11007381	Click to see CCCCCCCCCCCCCCCCCCCC=CCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCCCCCCCCCC)O)O)O	844.30	unknown	https://doi.org/10.1039/JR9380001685
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
2-[[3-Hydroxy-5-(10-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxolan-3-yl]methoxy]-6-methyloxane-3,4,5-triol	75034135	Click to see CC1CCC2(C(C3C(O2)CC4C3(C(CC5C4CC=C6C5(CCC(C6)OC7C(C(CO7)(COC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)O)C)C)OC1	855.00	unknown	https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1016/0031-9422(89)80374-7 https://doi.org/10.1271/BBB.58.1824
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine	5184	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1055/S-0028-1097183 https://doi.org/10.1055/S-0028-1099896
[(2R,4S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2R)-3-hydroxy-2-phenylpropanoate	134767951	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1016/0031-9422(91)83191-M https://doi.org/10.1248/CPB.39.1263 https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1300/J044V04N03_08 https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1271/BBB.58.1447 https://doi.org/10.1271/BBB.58.1443 https://doi.org/10.1055/S-2006-962085 https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1271/BBB.58.1820 https://doi.org/10.1271/BBB1961.53.863
Tropic acid ester with scopine	153311	Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4	303.35	unknown	https://doi.org/10.1016/0031-9422(91)83191-M https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1300/J044V04N03_08 https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1271/BBB.58.1447 https://doi.org/10.1271/BBB.58.1443 https://doi.org/10.1055/S-2006-962085 https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1271/BBB.58.1820 https://doi.org/10.1271/BBB1961.53.863
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
[NMe-Ser7]MC-RY	146684759	Click to see CC1C(NC(=O)C(NC(=O)C(C(NC(=O)C(NC(=O)C(NC(=O)C(N(C(=O)CCC(NC1=O)C(=O)O)C)CO)C)CCCN=C(N)N)C(=O)O)C)CC2=CC=C(C=C2)O)C=CC(=CC(C)C(CC3=CC=CC=C3)OC)C	1063.20	unknown	https://doi.org/10.1055/S-0028-1097183 https://doi.org/10.1055/S-0028-1099896
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Trialkylamines
N,N,N',N'-Tetramethyl-1,4-butanediamine	66074	Click to see CN(C)CCCCN(C)C	144.26	unknown	https://doi.org/10.1055/S-0028-1099896
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Pentatriacontan-4-one	86254883	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)CCC	506.90	unknown	https://doi.org/10.1016/S0031-9422(00)85030-X
> Organoheterocyclic compounds / Oxepanes
(1R,2S,3S,5R,6R,9R,10R,12S,16R,18S,20R,22R,23S,25R)-3,9,23-trihydroxy-22-methoxy-1,5,20-trimethyl-6-(5-oxo-2H-furan-3-yl)-11,17,19,24-tetraoxaheptacyclo[12.12.0.02,10.05,9.010,12.016,25.018,23]hexacos-14-en-4-one	21632918	Click to see CC1CC(C2(C(O1)OC3C=C4CC5C6(O5)C(C4(CC3O2)C)C(C(=O)C7(C6(CCC7C8=CC(=O)OC8)O)C)O)O)OC	574.60	unknown	https://doi.org/10.1016/0031-9422(91)85120-O
> Organoheterocyclic compounds / Piperidines
1-[(2R)-piperidin-2-yl]propan-2-one	3034881	Click to see CC(=O)CC1CCCCN1	141.21	unknown	https://doi.org/10.1039/JR9570003967
Pelletierine	92987	Click to see CC(=O)CC1CCCCN1	141.21	unknown	https://doi.org/10.1039/JR9570003967
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine	942	Click to see CN1CCCC1C2=CN=CC=C2	162.23	unknown	https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1248/CPB.39.1263 https://doi.org/10.1039/JR9570003967 https://doi.org/10.1248/CPB.33.5445
Nicotine	89594	Click to see CN1CCCC1C2=CN=CC=C2	162.23	unknown	https://doi.org/10.1271/BBB.58.1824 https://doi.org/10.1248/CPB.39.1263 https://doi.org/10.1039/JR9570003967 https://doi.org/10.1016/0031-9422(91)85120-O https://doi.org/10.1248/CPB.33.5445
> Organoheterocyclic compounds / Tetrapyrroles and derivatives / Chlorins
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	5459387	Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C	871.20	unknown	https://doi.org/10.1300/J044V04N03_08
methyl (3R,21S,22S)-16-ethenyl-11-ethyl-12,17,21,26-tetramethyl-4-oxo-22-[3-oxo-3-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]propyl]-7,23,24,25-tetrazahexacyclo[18.2.1.15,8.110,13.115,18.02,6]hexacosa-1(23),2(6),5(26),7,9,11,13,15,17,19-decaene-3-carboxylate	6433193	Click to see CCC1=C(C2=CC3=C(C(=C(N3)C=C4C(C(C(=N4)C5=C6C(=C(C(=N6)C=C1N2)C)C(=O)C5C(=O)OC)CCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C)C)C)C=C)C	871.20	unknown	https://doi.org/10.1300/J044V04N03_08
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
Hermandiol	5318019	Click to see CC(CO)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O	262.26	unknown	https://doi.org/10.1016/0031-9422(92)80490-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (2S)-3-hydroxy-2-methylpropanoate	163030082	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)OC6C(C(C(C(O6)COC(=O)C(C)CO)O)O)O	842.70	unknown	https://doi.org/10.1055/S-2007-969571 https://doi.org/10.1248/CPB.33.5445 https://doi.org/10.1248/CPB.39.1263 https://doi.org/10.1271/BBB.58.1824
3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162890784	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)C(C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	578.50	unknown	https://doi.org/10.1039/JR9370001820
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-[7-Hydroxy-5-methoxy-2-methyl-2-(4-methylpent-3-enyl)chromen-8-yl]-3-phenylprop-2-en-1-one	5256732	Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)C(=O)C=CC3=CC=CC=C3)O)OC)C)C	404.50	unknown	https://doi.org/10.1055/S-0028-1099896

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Duboisia myoporoides

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top