PlantaeDB Logo
Login Sign-up

Morus insignis

We don't have an image yet. Upload an image!

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 UUID643ffde3a8eaf290017600
Scientific name Morus insignis
Authority Bureau
First published in Prodr. 17: 247 (1873)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Morus marmolii Legname Lilloa 33: 334 (1973)
Morus peruviana Planch. ex Koidz. Fl. Symb. Orient.-Asiat. : 88 (1930)
Morus trianae J.-F.Leroy Bull. Mus. Natl. Hist. Nat. , sér. 2, 21: 731 (1950)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Arabic توت مميز
Quechua antikuna murira

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000447882
Tropicos 21300266
KEW urn:lsid:ipni.org:names:316991-2
The Plant List kew-2501349
Open Tree Of Life 868040
NCBI Taxonomy 1031565
IUCN Red List 151272201
IPNI 316991-2
iNaturalist 283986
GBIF 5569971
Wikipedia Paratrophis_insignis

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
Identification and Antioxidant Capacity of Free and Bound Phenolics in Six Varieties of Mulberry Seeds Using UPLC-ESI-QTOF-MS/MS Gao H, Guo M, Wang L, Sun C, Huang L Antioxidants (Basel) 07-Sep-2022
PMCID:PMC9495565
doi:10.3390/antiox11091764
PMID:36139838
Dietary preferences and feeding strategies of Colombian highland woolly monkeys Fonseca ML, Ramírez-Pinzón MA, McNeil KN, Guevara M, Gómez-Gutiérrez LM, Harter K, Mongui A, Stevenson PR Sci Rep 23-Aug-2022
PMCID:PMC9399098
doi:10.1038/s41598-022-17655-5
PMID:35999220
Phytochemical Composition of Different Botanical Parts of Morus Species, Health Benefits and Application in Food Industry Memete AR, Timar AV, Vuscan AN, Miere (Groza) F, Venter AC, Vicas SI Plants (Basel) 06-Jan-2022
PMCID:PMC8777750
doi:10.3390/plants11020152
PMID:35050040
Structural Revision of Sesbagrandiflorains A and B, and Synthesis and Biological Evaluation of 6-Methoxy-2-arylbenzofuran Derivatives Noviany N, Samadi A, Carpenter EL, Abugrain ME, Hadi S, Purwitasari N, Indra G, Indra A, Mahmud T J Nat Med 18-Aug-2020
PMCID:PMC7791000
doi:10.1007/s11418-020-01445-2
PMID:32809097
Components of the Root Bark of Morus insignis Bur. 1. Structures of Four New Isoprenylated Xathones, Morusignins A, B, C, and D Taro Nomura, Yoshio Hano, Tsuyoshi Okamoto, Yasunori Momose The Japan Institute of Heterocyclic Chemistry 16-Apr-2009
doi:10.3987/COM-90-5420
Components of the Root Bark of Morus insignis Bur. 3. Structures of Three New Isoprenylated Xanthones Morusignins I, J, and K and an Isoprenylated Flavone Morusignin L. Taro Nomura, Yoshio Hano, Tsuyoshi Okamoto, Katsue Suzuki, Masami Negishi The Japan Institute of Heterocyclic Chemistry 06-Mar-2009
doi:10.3987/COM-92-6320
Components of the Root Bark of Morus insignis Bur. 2. Structures of Four New Isoprenylated Xanthones, Morusignins E, F, G. and H Taro Nomura, Yoshio Hano, Tsuyoshi Okamoto The Japan Institute of Heterocyclic Chemistry 03-Mar-2009
doi:10.3987/COM-91-5754
Two new 2-arylbenzofuran derivatives from hypoglycemic activity-bearing fractions of Morus insignis. Basnet P, Kadota S, Terashima S, ShimizuM, Namba T Chem Pharm Bull (Tokyo) 01-Jul-1993
doi:10.1248/CPB.41.1238
PMID:8374993

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
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(2S,3S,4R,5R,6S)-2-[(3S,4E,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-hydroxy-25-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-2,6,10,14,19,23-hexamethylpentacosa-4,6,8,10,12,14,16,18,20,22,24-undecaen-3-yl]oxy-6-methyloxane-3,4,5-triol 162905296 Click to see CC1C(C(C(C(O1)OC(C=CC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C)C)C(C)(C)O)O)O)O 731.00 unknown https://doi.org/10.3987/COM-91-5754
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-10-hydroxy-6a-[4-(4-hydroxy-3-methoxyphenyl)-2-oxobut-3-enyl]-1,2,6b,9,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 163094600 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)CC(=O)C=CC6=CC(=C(C=C6)O)OC)C(=O)O 632.90 unknown https://doi.org/10.1248/CPB.41.1238
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/10.1248/CPB.41.1238
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/10.1248/CPB.41.1238
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(2R,3R,4S,5S,6S)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496016 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.41.1238
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.41.1238
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.41.1238
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1248/CPB.41.1238
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.41.1238
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/CPB.41.1238
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(2S)-5,10-dihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-enyl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 163001119 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC=C4)O)CC(O2)C(C)(C)O)C 396.40 unknown https://doi.org/10.3987/COM-91-5754
(2S)-5,7,10-trihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-enyl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 163077098 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(C=CC(=C4O3)O)O)CC(O2)C(C)(C)O)C 412.40 unknown https://doi.org/10.3987/COM-91-5754
1,3,6-Trihydroxy-5-methoxy-2-prenylxanthone 14886043 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3OC)O)O)C 342.30 unknown https://doi.org/10.3987/COM-90-5420
5,10-Dihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-enyl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 21591068 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC=C4)O)CC(O2)C(C)(C)O)C 396.40 unknown https://doi.org/10.3987/COM-91-5754
5,7,10-Trihydroxy-2-(2-hydroxypropan-2-yl)-4-(3-methylbut-2-enyl)-1,2-dihydrofuro[2,3-c]xanthen-6-one 21591067 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(C=CC(=C4O3)O)O)CC(O2)C(C)(C)O)C 412.40 unknown https://doi.org/10.3987/COM-91-5754
garcinone B 5495928 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(C(=C3)O)OC(C=C4)(C)C)O)C 394.40 unknown https://doi.org/10.3987/COM-90-5420
Morusignin B 14492422 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C=CC(=C3C2=O)O)O)O)C 328.30 unknown https://doi.org/10.3987/COM-90-5420
Morusignin J 71452951 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(C=CC(=C4O3)O)O)C=CC(O2)(C)C)C 394.40 unknown https://doi.org/10.3987/COM-92-6320
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(2S)-4,6,9-trihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 162932189 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C=CC(=C4C3=O)O)O)O)CC(O2)C(C)(C)O)C 412.40 unknown https://doi.org/10.3987/COM-91-5754
(2S)-4,9-dihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 162987335 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)CC(O2)C(C)(C)O)C 396.40 unknown https://doi.org/10.3987/COM-91-5754
1,3,5,8-Tetrahydroxy-4-(3-methylbut-2-enyl)xanthen-9-one 14886041 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(C=CC(=C3O2)O)O)C 328.30 unknown https://doi.org/10.3987/COM-90-5420
1,3,6-Trihydroxy-7-methoxy-5-(3-methylbut-2-enyl)xanthen-9-one 85698156 Click to see CC(=CCC1=C2C(=CC(=C1O)OC)C(=O)C3=C(C=C(C=C3O2)O)O)C 342.30 unknown https://doi.org/10.3987/COM-92-6320
4,6,9-Trihydroxy-2-(2-hydroxypropan-2-yl)-11-(3-methylbut-2-enyl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 15705036 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C=CC(=C4C3=O)O)O)O)CC(O2)C(C)(C)O)C 412.40 unknown https://doi.org/10.3987/COM-91-5754
5,7,10-Trihydroxy-2,2-dimethyl-12-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one 86276121 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C=CC(=C4C3=O)O)O)O)C=CC(O2)(C)C)C 394.40 unknown https://doi.org/10.3987/COM-92-6320
Gartanin 5281633 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(C=CC(=C3O2)O)O)CC=C(C)C)O)C 396.40 unknown https://doi.org/10.3987/COM-90-5420
Ugaxanthone 5321880 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=C(C=C3)O)O)C 328.30 unknown https://doi.org/10.3987/COM-90-5420
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6,8,11-Trihydroxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one 14886042 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C=CC(=C4C3=O)O)O)O)C 326.30 unknown https://doi.org/10.3987/COM-90-5420
toxyloxanthone B 14886044 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(C=C(C=C4O3)O)O)O)C 326.30 unknown https://doi.org/10.3987/COM-90-5420
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4S,5S,6S)-2-[3-hydroxy-5-(6-hydroxy-1-benzofuran-2-yl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162903527 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 404.40 unknown https://doi.org/10.1248/CPB.41.1238
[(1R,2S,6S)-2-[2,6-dihydroxy-4-[6-hydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-2-yl]phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(2,4-dihydroxyphenyl)methanone 102469749 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C(=C(C=C6)O)CC=C(C)C)O 648.70 unknown https://doi.org/10.1248/CPB.41.1238
[2-[2,6-Dihydroxy-4-[6-hydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-2-yl]phenyl]-6-(2,4-dihydroxyphenyl)-4-methylcyclohex-3-en-1-yl]-(2,4-dihydroxyphenyl)methanone 74935356 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C(=C(C=C6)O)CC=C(C)C)O 648.70 unknown https://doi.org/10.1248/CPB.41.1238
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 242.23 unknown https://doi.org/10.1248/CPB.41.1238
Moracin M-3'-O-glucopyranoside 197721 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 404.40 unknown https://doi.org/10.1248/CPB.41.1238
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Morusignin L 44258298 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=C(O3)C4=C(C=C(C=C4)O)O)CCC(C)(C)O)C 438.50 unknown https://doi.org/10.3987/COM-92-6320
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.41.1238
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.41.1238
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.41.1238
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.41.1238
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.41.1238
Quercetin 3-alloside 12304327 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.41.1238
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Lupinisoflavone A 5319901 Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O 352.30 unknown https://doi.org/10.3987/COM-91-5754

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.