Scientific name	Authority	First published in
Morus caudatifolia	Koidz.	Icon. Pl. Koisikav. 3: 79 (1916)
Morus cashmeriana	Royle	Ill. Bot. Himal. Mts. : 337 (1839)
Morus expansa	hort. ex Raf.	Amer. Man. Mulberry Trees : 26 (1839)
Morus hachijoensis	(Hotta) Hotta	Acta Phytotax. Geobot. 13: 144 (1943)
Morus arabica	Koidz.	Bot. Mag. (Tokyo) 31: 35 (1917)
Morus amamiana	Nakai	J. Jap. Bot. 25: 131 (1950)
Morus kagayamae	Koidz.	Icon. Pl. Koisikav. 3: 11 (1915)
Morus latifolia	Poir.	Encycl. 4: 381 (1797)
Morus mizuho	Hotta	Bot. Mag. (Tokyo) 51: 834 (1937)
Morus rotundiloba	Koidz.	Bot. Mag. (Tokyo) 31: 36 (1917)
Morus stylosa	Ser.	Descr. Mûriers : 225 (1855)
Morus bombycis	Koidz.	Bot. Mag. (Tokyo) 29: 313 (1915)
Morus mizuho	Hotta	Bot. Mag. (Tokyo) 51: 834 (1937)
Morus australis	Poir.	Encycl. 4: 380 (1797)
Morus longistylus	Diels	Notes Roy. Bot. Gard. Edinburgh 5: 293 (1912)
Morus cavaleriei	H.Lév.	Repert. Spec. Nov. Regni Veg. 10: 146 (1911)
Morus inusitata	H.Lév.	Repert. Spec. Nov. Regni Veg. 13: 265 (1914)
Morus acidosa	Griff.	Not. Pl. Asiat. 4: 388 (1854)
Morus formosensis	Hotta	Acta Phytotax. Geobot. 6: 142 (1937)
Morus australis var. oblongifolia	Z.Y.Cao	Acta Bot. Yunnan. 17: 154 (1995)
Morus hastifolia	F.T.Wang & Tang ex Z.Y.Cao	Acta Phytotax. Sin. 29: 266 (1991)
Morus australis var. inusitata	(Lévl.) C.Y.Wu	Acta Bot. Yunnan. 11: 25 (1989)
Morus australis var. incisa	C.Y.Wu	Acta Bot. Yunnan. 11: 26 (1989)
Morus australis var. hastifolia	(Z.Y.Cao) Z.Y.Cao	Acta Bot. Yunnan. 17: 158 (1995)
Morus australis var. linearipartita	Z.Y.Cao	Acta Bot. Yunnan. 17: 158 (1995)
Morus alba var. nigriformis	Bureau
Morus alba var. stylosa	Bureau
Morus bombycis var. angustifolia	Koidz.
Morus bombycis var. bifida	Koidz.
Morus bombycis var. longistyla	Koidz.
Morus bombycis var. tiliifolia	Koidz.
Morus stylosa var. ovalifolia	Ser.
Morus australis var. hachijoensis	(Hotta) Kitam.	Acta Phytotax. Geobot. 28: 19 (1977)
Morus bombycis var. flexuosa	Hotta	Acta Phytotax. Geobot. 25: 55 (1972)
Morus bombycis var. ikuchuensis	Hotta	Acta Phytotax. Geobot. 25: 55 (1972)
Morus bombycis var. mikamiana	Hotta	Acta Phytotax. Geobot. 25: 55 (1972)
Morus bombycis var. saishuensis	Hotta	Acta Phytotax. Geobot. 25: 186 (1973)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Middle Atlantic Ocean
  - Ascension
- Northeast Tropical Africa
  - Eritrea
  - Ethiopia
  - Sudan
- Southern Africa
  - Northern Provinces
- West-central Tropical Africa
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Comoros
  - Mauritius
  - Réunion

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Manchuria
  - Tibet
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan
- Middle Asia
  - Uzbekistan
- Russian Far East
  - Kuril Islands
  - Sakhalin

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - South China Sea
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Philippines

Europe click to expand
- Southwestern Europe
  - Spain

Pacific click to expand
- Northwestern Pacific
  - Marianas
- South-central Pacific
  - Cook Islands
  - Society Islands
  - Tuamotu
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - Vanuatu

Southern America click to expand
- Caribbean
  - Trinidad-Tobago

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000447884
Tropicos	21300012
Flora of Italy	11388
KEW	urn:lsid:ipni.org:names:854652-1
The Plant List	kew-2501351
Open Tree Of Life	307703
NCBI Taxonomy	248361
IPNI	854652-1
iNaturalist	773801
GBIF	5569978
USDA GRIN	24614
Wikipedia	Morus_indica
CMAUP	NPO11796
CMAUP	NPO16194

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_029231665.1	JNU_Mind_1.1	Scaffold	Jawaharlal Nehru University	2023-03-17	293.0x	481.89 Mb

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 characterization of the Remorin gene family in Saccharum and the involvement of ScREM1.5e-1/-2 in SCMV infection on sugarcane

Yang Z, Cheng G, Yu Q, Jiao W, Zeng K, Luo T, Zhang H, Shang H, Huang G, Wang F, Guo Y, Xu J

Front Plant Sci

23-Feb-2024

PMCID:	PMC10920289
doi:	10.3389/fpls.2024.1365995
PMID:	38463560

First Report on Mesophyll Protoplast Isolation and Regeneration System for the Duboisia Species

Xue Y, Hiti-Bandaralage JC, Hu Z, Zhao Z, Mitter N

Plants (Basel)

21-Dec-2023

PMCID:	PMC10780843
doi:	10.3390/plants13010040
PMID:	38202348

Diversity of fungal pathogens in leaf spot disease of Indian mulberry and its management

GS A, Mayavathi NR NP, N.R. A, B.M. M, Sherpa DC, C A, Suresh A, Kammar S, M S, S S, B.N. G, Doss S G

Heliyon

02-Nov-2023

PMCID:	PMC10665727
doi:	10.1016/j.heliyon.2023.e21750
PMID:	38027777

The role of WRKY transcription factors, FaWRKY29 and FaWRKY64, for regulating Botrytis fruit rot resistance in strawberry (Fragaria × ananassa Duch.)

Lee MB, Han H, Lee S

BMC Plant Biol

11-Sep-2023

PMCID:	PMC10494375
doi:	10.1186/s12870-023-04426-1
PMID:	37691125

Summary of drug therapy to treat cognitive impairment-induced obstructive sleep apnea

He D, Chen J, Du X, Xu L

Front Cell Neurosci

04-Sep-2023

PMCID:	PMC10507626
doi:	10.3389/fncel.2023.1222626
PMID:	37731463

Unearthing the fungal endophyte Aspergillus terreus for chemodiversity and medicinal prospects: a comprehensive review

Amr K, Ibrahim N, Elissawy AM, Singab AN

Fungal Biol Biotechnol

25-Mar-2023

PMCID:	PMC10040139
doi:	10.1186/s40694-023-00153-2
PMID:	36966331

Bio-Actives from Natural Products with Potential Cardioprotective Properties: Isolation, Identification, and Pharmacological Actions of Apigenin, Quercetin, and Silibinin

Tomou EM, Papakyriakopoulou P, Skaltsa H, Valsami G, Kadoglou NP

Molecules

05-Mar-2023

PMCID:	PMC10005323
doi:	10.3390/molecules28052387
PMID:	36903630

Anti-inflammatory therapy of atherosclerosis: focusing on IKKβ

Gan J, Guo L, Zhang X, Yu Q, Yang Q, Zhang Y, Zeng W, Jiang X, Guo M

J Inflamm (Lond)

23-Feb-2023

PMCID:	PMC9951513
doi:	10.1186/s12950-023-00330-5
PMID:	36823573

Enhancing plant growth promoting rhizobacterial activities through consortium exposure: A review

Singh A, Yadav VK, Chundawat RS, Soltane R, Awwad NS, Ibrahium HA, Yadav KK, Vicas SI

Front Bioeng Biotechnol

10-Feb-2023

PMCID:	PMC9972119
doi:	10.3389/fbioe.2023.1099999
PMID:	36865031

Optimized Recovery of Cryostored Dormant Buds of Mulberry Germplasm

Choudhary R, Malik SK, Chaudhury R, Rao AA

Plants (Basel)

04-Jan-2023

PMCID:	PMC9867320
doi:	10.3390/plants12020225
PMID:	36678937

Protective Application of Morus and Its Extracts in Animal Production

Wang L, Gao H, Sun C, Huang L

Animals (Basel)

15-Dec-2022

PMCID:	PMC9774465
doi:	10.3390/ani12243541
PMID:	36552461

Environmental stress - what can we learn from chlorophyll a fluorescence analysis in woody plants? A review

Swoczyna T, Kalaji HM, Bussotti F, Mojski J, Pollastrini M

Front Plant Sci

14-Dec-2022

PMCID:	PMC9795016
doi:	10.3389/fpls.2022.1048582
PMID:	36589121

Jack of all trades: Genome assembly of Wild Jack and comparative genomics of Artocarpus

Patil AB, Vajja SS, Raghavendra S, Satish BN, Kushalappa CG, Vijay N

Front Plant Sci

12-Dec-2022

PMCID:	PMC9791056
doi:	10.3389/fpls.2022.1029540
PMID:	36578332

The complete chloroplast genome sequences of three Broussonetia species and comparative analysis within the Moraceae

Yang J, Chu Q, Meng G, Kong W

PeerJ

31-Oct-2022

PMCID:	PMC9632464
doi:	10.7717/peerj.14293
PMID:	36340196

p-Coumaroylation of lignin occurs outside of commelinid monocots in the eudicot genus Morus (mulberry)

Hellinger J, Kim H, Ralph J, Karlen SD

Plant Physiol

21-Oct-2022

PMCID:	PMC9922387
doi:	10.1093/plphys/kiac485
PMID:	36269202

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 / Tropane alkaloids
(-)-calystegine B2	23642747	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
8-Azabicyclo[3.2.1]octane-1,2,3,4-tetraol	3693124	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
Calystegin B2	443000	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
Calystegine B2	124434	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
CID 384346	384346	Click to see C1CC2(C(C(C(C1N2)O)O)O)O	175.18	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Acylaminobenzoic acid and derivatives
4-[(2-amino-4-oxo-1H-pteridin-6-yl)methyl-formylamino]benzoic acid	97575	Click to see C1=CC(=CC=C1C(=O)O)N(CC2=CN=C3C(=N2)C(=O)N=C(N3)N)C=O	340.29	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl benzoate	7165	Click to see CCOC(=O)C1=CC=CC=C1	150.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid	243	Click to see C1=CC=C(C=C1)C(=O)O	122.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	via CMAUP database
> Benzenoids / Naphthalenes
Naphthalene	931	Click to see C1=CC=C2C=CC=CC2=C1	128.17	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Coniferyl alcohol	1549095	Click to see COC1=C(C=CC(=C1)C=CCO)O	180.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid	3931	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
9,12-Octadecadienoic acid, (E,Z)-	5282798	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
9Z,12E-octadecadienoic acid	5282797	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linoelaidic acid	5282457	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linoleate	5460332	Click to see CCCCCC=CCC=CCCCCCCCC(=O)[O-]	279.40	unknown	via CMAUP database
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid	5280896	Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene	5280489	Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C	536.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	45483610	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	via CMAUP database
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	92835934	Click to see CC12CCCCC1C(CC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
(3beta,5alpha,7alpha)-3,7-Dihydroxyandrostan-17-one	9815044	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,7S,8R,9S,10S,13S,14S)-3,7-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	57386710	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S,17S)-3,17-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	69924431	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3R,5R,8R,9S,10S,13S,14S)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,8,9,11,12,14,15,16-dodecahydro-1H-cyclopenta[a]phenanthrene-7,17-dione	57386713	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
(3R,5S,6S,8R,9S,10R,13S,14S)-3,6-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one	69766330	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
(3S,5R,7R,8S,9S,10S,13R,14S,16S)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,7,16-triol	99574281	Click to see CC12CCC3C(C1CC(C2)O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5R,7S,8S,9S,10S,13S,14S,16S)-3,7,16-trihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99572894	Click to see CC12CCC(CC1CC(C3C2C(=O)CC4(C3CC(C4)O)C)O)O	322.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573267	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5R,8S,9S,10S,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-7-one	99573266	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,6S,8S,9S,10R,13R,14S,16R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6,16-triol	99574278	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571962	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10R,13R,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one	99571961	Click to see CC12CCC3C(C1CC(C2)O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99601533	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(3S,5S,8S,9S,10S,13S,14S,16S)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-11-one	99575783	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
(5R,8S,9S,10S,13R,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,7-dione	99571971	Click to see CC12CCC3C(C1CC(C2)O)C(=O)CC4C3(CCC(=O)C4)C	304.40	unknown	via CMAUP database
(5S,6R,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573707	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16R)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573706	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10R,13R,14S,16S)-6,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99573705	Click to see CC12CCC3C(C1CC(C2)O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
(5S,6S,8S,9S,10S,11R,13S,14S)-6,11-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one	99574441	Click to see CC12CCCC1C3CC(C4CC(=O)CCC4(C3C(C2)O)C)O	306.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16R)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571360	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9R,10S,13S,14S,16S)-9,16-dihydroxy-10,13-dimethyl-1,2,4,5,6,7,8,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthrene-3,11-dione	99571358	Click to see CC12CCC(=O)CC1CCC3C2(C(=O)CC4(C3CC(C4)O)C)O	320.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16R)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574177	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
(5S,8S,9S,10S,13S,14S,16S)-16-hydroxy-10,13-dimethyl-2,4,5,6,7,8,9,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,11-dione	99574175	Click to see CC12CCC(=O)CC1CCC3C2C(=O)CC4(C3CC(C4)O)C	304.40	unknown	via CMAUP database
11-Hydroxyandrosterone	21139727	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
11alpha-Hydroxy-5alpha-androstane-3,17-dione	101709630	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
11alpha,16alpha-Dihydroxy-5alpha-androstan-3-one	100922644	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CC(C4)O)C)O	306.40	unknown	via CMAUP database
3beta-Hydroxy-5alpha-androstane-7,17-dione	11954160	Click to see CC12CCC(CC1CC(=O)C3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
3beta,6alpha,17beta-Trihydroxy-5alpha-androstane	170796	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
5,17beta-Dihydroxy-5alpha-androstane-3-one	10979706	Click to see CC12CCC3C(C1CCC2O)CCC4(C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-11-one, 3alpha,17beta-dihydroxy-	10125601	Click to see CC12CCC(CC1CCC3C2C(=O)CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3-one, 11alpha,17beta-dihydroxy-	22796602	Click to see CC12CCC(=O)CC1CCC3C2C(CC4(C3CCC4O)C)O	306.40	unknown	via CMAUP database
5alpha-Androstan-3beta,17beta-diol-7-one	11868973	Click to see CC12CCC3C(C1CCC2O)C(=O)CC4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstan-6-one, 3beta,17beta-dihydroxy-	11551286	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
5alpha-Androstane-3,7,17-trione	11266632	Click to see CC12CCC(=O)CC1CC(=O)C3C2CCC4(C3CCC4=O)C	302.40	unknown	via CMAUP database
5alpha-Androstane-3beta,11alpha,16beta-triol	100922640	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CC(C4)O)C)O)O	308.50	unknown	via CMAUP database
5alpha-Androstane-3beta,11alpha,17beta-triol	57396177	Click to see CC12CCC(CC1CCC3C2C(CC4(C3CCC4O)C)O)O	308.50	unknown	via CMAUP database
6alpha-Hydroxy-EPIA	15917986	Click to see CC12CCC(CC1C(CC3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
7-beta-Hydroxyepiandrosterone	9836181	Click to see CC12CCC(CC1CC(C3C2CCC4(C3CCC4=O)C)O)O	306.40	unknown	via CMAUP database
Androstan-3-one, 6,17-dihydroxy-, (5alpha,6alpha,17beta)-	15838416	Click to see CC12CCC3C(C1CCC2O)CC(C4C3(CCC(=O)C4)C)O	306.40	unknown	via CMAUP database
Androstan-6-one, 3,17-dihydroxy-, (3alpha,5alpha,17beta)-	15929496	Click to see CC12CCC3C(C1CCC2O)CC(=O)C4C3(CCC(C4)O)C	306.40	unknown	via CMAUP database
Androstane-3,17-dione, 6-hydroxy-, (5alpha,6alpha)-	22296022	Click to see CC12CCC(=O)CC1C(CC3C2CCC4(C3CCC4=O)C)O	304.40	unknown	via CMAUP database
Jgd4N79M5A	68995028	Click to see CC12CCC3C(C1CCC2O)C(CC4C3(CCC(C4)O)C)O	308.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
10-Hydroxy-3-oxoestr-4-en-17-yl acetate	91691749	Click to see CC(=O)OC1CCC2C1(CCC3C2CCC4=CC(=O)CCC34O)C	332.40	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-6-amino-2-azaniumylhexanoate	122198194	Click to see C(CCN)CC(C(=O)[O-])[NH3+]	146.19	unknown	via CMAUP database
[(1S)-5-amino-1-carboxypentyl]azanium	24848423	Click to see C(CCN)CC(C(=O)O)[NH3+]	147.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Gamma amino acids and derivatives
4-Aminobutanoate	6992099	Click to see C(CC(=O)[O-])C[NH3+]	103.12	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
Glutaric acid	743	Click to see C(CC(=O)O)CC(=O)O	132.11	unknown	via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
2-Oxonioacetate	3698251	Click to see C(C(=O)[O-])[OH2+]	76.05	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,4-Dicaffeoylquinic acid	12358846	Click to see C1C(C(C(CC1(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	via CMAUP database
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Chlorogensaure	12310830	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
cis-Chlorogenic acid	1794425	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol	892	Click to see C1(C(C(C(C(C1O)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
3-Glucopyranosylfagomine	10852369	Click to see C1CNC(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)CO	309.31	unknown	via CMAUP database
4-Glucopyranosylfagomine	21591966	Click to see C1CNC(C(C1O)OC2C(C(C(C(O2)CO)O)O)O)CO	309.31	unknown	via CMAUP database
alpha-D-Glucopyranoside, beta-D-fructofuranosyl	91692850	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose NF	46782954	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-Fructose	2723872	Click to see C1C(C(C(C(O1)(CO)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(4S,5R)-6-methyloltetrahydropyran-2,3,4,5-tetrol	59083882	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
alpha-D-GALACTOSE	439357	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
D-Galactose	6036	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
D-Glucose	5793	Click to see C(C1C(C(C(C(O1)O)O)O)O)O	180.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone	7469	Click to see CC(=O)C1=CC=C(C=C1)O	136.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one	12311356	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid	54670067	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	via CMAUP database
D-ascorbic acid	54690394	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	via CMAUP database
L-[2-13C]ascorbic acid	54676536	Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O	176.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Indolizidines
Castanospermine	54445	Click to see C1CN2CC(C(C(C2C1O)O)O)O	189.21	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines
(2S,3S,4S,5R)-2-Hydroxymethyl-piperidine-3,4,5-triol	44387838	Click to see C1C(C(C(C(N1)CO)O)O)O	163.17	unknown	via CMAUP database
1-Deoxynojirimycin	29435	Click to see C1C(C(C(C(N1)CO)O)O)O	163.17	unknown	via CMAUP database
1-Deoxynojirimycin hydrochloride	377339	Click to see C1C(C(C(C(N1)CO)O)O)O.Cl	199.63	unknown	via CMAUP database
3-Epi-fagomine	10290867	Click to see C1CNC(C(C1O)O)CO	147.17	unknown	via CMAUP database
Fagomine	72259	Click to see C1CNC(C(C1O)O)CO	147.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines
1,4-Dideoxy-1,4-imino-d-arabinitol	451991	Click to see C1C(C(C(N1)CO)O)O	133.15	unknown	via CMAUP database
2,5-Dideoxy-2,5-imino-D-mannitol	124702	Click to see C(C1C(C(C(N1)CO)O)O)O	163.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinoline carboxylic acids
Quininic acid	345824	Click to see COC1=CC2=C(C=CN=C2C=C1)C(=O)O	203.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(1R,2S,5S)-5-[2,6-dihydroxy-4-(6-hydroxy-1-benzofuran-2-yl)phenyl]-2-(2,4-dihydroxyphenyl)-3-methylcyclohex-3-en-1-yl]-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]methanone	5458824	Click to see CC1=CC(CC(C1C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O	648.70	unknown	via CMAUP database
17-(6-Hydroxy-2,3-dihydro-1-benzofuran-2-yl)-1-[(5-hydroxy-2,2-dimethylchromen-8-yl)methyl]-11-methyl-2,20-dioxapentacyclo[11.7.1.03,8.09,21.014,19]henicosa-3(8),4,6,11,14,16,18-heptaene-5,15-diol	5319927	Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6CC7=C(O6)C=C(C=C7)O)CC8=C9C(=C(C=C8)O)C=CC(O9)(C)C	644.70	unknown	via CMAUP database
Chalcomoracin	434768	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)CC=C(C)C)O)C4=C(C=C(C=C4O)C5=CC6=C(O5)C=C(C=C6)O)O	648.70	unknown	via CMAUP database
Mulberrofuran C	157143	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)O	580.60	unknown	via CMAUP database
Mulberrofuran F	3086294	Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC(=CC(=C25)O)C6=CC7=C(O6)C=C(C=C7)O)C8=C(C(=C(C=C8)O)CC=C(C)C)O	630.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
Broussoaurone A	15298907	Click to see CC(=CCC1=CC2=C(C=C1O)OC(=CC3=CC(=C(C=C3)O)O)C2=O)C	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid	444539	Click to see C1=CC=C(C=C1)C=CC(=O)O	148.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid	1549106	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O	178.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(E)-1-[3-[(1S,5S,6R)-6-[3,5-dihydroxy-4-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(2,4-dihydroxyphenyl)prop-2-en-1-one	45485201	Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=CC(=C(C(=C3)O)CC=C(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=C(C=C(C=C5)O)O)O	678.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans
Broussoflavan A	44257178	Click to see CC(=CCC1=C(C2=C(C=C1C3CCC4=C(O3)C=C(C=C4)O)C(C(C(O2)(C)C)O)O)O)C	426.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Norartocarpetin	5481970	Click to see C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
Broussoflavonol G	10368916	Click to see CC(=CCC1=C(C(=C(C=C1C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)O)CC=C(C)C)C	506.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Morusin	5281671	Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=C(C=C(C=C4)O)O)C	420.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Broussoflavonol F	9866908	Click to see CC(=CCC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C	422.50	unknown	via CMAUP database
Mulberrin	5481958	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)C	422.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
Quercetin hydrate	16212154	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O.O	320.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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	via CMAUP database
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	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Cyclomorusin	5481969	Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O)C	418.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Isobavachalcone	5281255	Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C	324.40	unknown	via CMAUP database
Morachalcone A	9862769	Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C	340.40	unknown	via CMAUP database

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Morus indica

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