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Diospyros ferrea

Diospyros ferrea - 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 UUID6440174fcd3c0693078809
Scientific name Diospyros ferrea
Authority (Willd.) Bakh.
First published in Gard. Bull. Straits Settlem. 7: 162 (1933)

Description Top

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Synonyms Top

Scientific name Authority First published in
Maba vacciniifolia Benth. Niger Fl. : 442 (1849)
Maba angustifolia Miq. Nieuwe Verh. Eerste Kl. Kon. Ned. Inst. Wetensch. Amsterdam , ser. 3, 5: 13 (1852)
Maba buxifolia Pers. Syn. Pl. 2: 606 (1807)
Maba ebenoxylon G.Don Gen. Hist. 4: 43 (1837)
Maba cumingiana A.DC. Prodr. 8: 241 (1844)
Maba papuana Hiern Nova Guinea 8: 199 (1909)
Maba nigrescens Dalzell Bombay Fl. : 142 (1861)
Maba smeathmannii A.DC. Prodr. 8: 241 (1844)
Maba secundiflora Hutch. Bull. Misc. Inform. Kew 1921: 384 (1921)
Maba lamponga Miq. Fl. Ned. Ind., Eerste Bijv. : 584 (1861)
Maba guineensis A.DC. Prodr. 8: 241 (1844)
Maba madagascariensis A.DC. Prodr. 8: 241 (1844)
Diospyros egbert-walkeri Kosterm. Blumea 23: 457 (1977)
Diospyros ferrea f. angustata Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 433 1941
Diospyros ferrea var. angustifolia (Miq.) Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 57 1937
Diospyros ferrea var. aroeensis Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 57. 1937
Diospyros ferrea var. buxifolia (Rottb.) Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 57. 1937
Diospyros ferrea var. buxoides Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 432. 1941
Diospyros ferrea var. ellipsoidea Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 433. 1941
Diospyros ferrea f. globosa Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 433 1941
Diospyros ferrea var. guineensis (Schumach. & Thonn.) Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 433. 1941
Diospyros ferrea var. indonesica Bakh. Bull. Jard. Bot. Buitenzorg sér. 3, 15: 433. 1941
Diospyros ferrea var. lamponga (Miq.) Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 434 1941
Diospyros ferrea f. lamponga (Miq.) Bakh. Bulletin du Jardin Botanique de Buitenzorg Series 3 15 1937
Diospyros ferrea f. oblanceolata Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 432 1941
Diospyros ferrea f. oblonga Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 432 1941
Diospyros ferrea f. oblongata Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 434 1941
Diospyros ferrea f. obovata Bakh. Bull. Jard. Bot. Buitenzorg III, 15: 434 1941
Diospyros ferrea var. salomonensis Bakh. Bull. Jard. Bot. Buitenzorg , sér. 3, 15: 57 (1937)
Diospyros ferrea f. subelliptica Bakh. Bull. Jard. Bot. Buitenzorg , sér. 3, 15: 432 (1941)
Diospyros nigrescens (Dalzell) C.J.Saldanha Fl. Hassan Distr. : 197 (1976)
Diospyros salomonensis (Bakh.) Kosterm. Ceylon J. Sci., Biol. Sci. 12: 100 (1977)
Diospyros vera (Lour.) A.Chev. Cat. Pl. Jard. Bot. Saigon : 31 (1919)
Ebenoxylum verum Lour. Fl. Cochinch. : 613 (1790)
Ebenus lamponga (Miq.) Kuntze Revis. Gen. Pl. 2: 408. 1891 [5 Nov 1891]
Ebenus nigrescens (Dalzell) Kuntze Revis. Gen. Pl. 2: 408. 1891 [5 Nov 1891]
Ferreola buxifolia Roxb. Pl. Coromandel 1: 35 (1795)
Ferreola ebenus Stokes Bot. Mat. Med. 4: 556 (1812)
Ferreola guineensis Schumach. & Thonn. Beskr. Guin. Pl. : 448 (1827)
Maba caningiana A.DC.
Maba neilgherrensis A.DC.
Diospyros ferrea var. angustifolia (Miq.) M.Mohanan Fl. Thiruvananthapuram 279. 1994
Maba egbert-walkeri (Kosterm.) F.Y.Lu, C.H.Ou, Y.T.Chen, Y.S.Chi, K.C.Lu & Y.H.Tseng Trees Taiwan 3: 69 (2010)
Maba ferrea (Willd.) S.S.Ying Coloured Ill. Fl. Taiwan 6: 38 (1998)

Common names Top

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Language Common/alternative name
ceb diospyros vera
Japanese 八重山黒檀
Japanese ヤエヤマコクタン
Oriya ଗୁଆକୋଳି
Swedish diospyros vera
Tamil இறும்பிலி
Thai ลำบิดทะเล
Vietnamese diospyros vera
war diospyros vera
Chinese 烏皮石柃
Chinese 象牙柿
Chinese 象牙树
Chinese 象牙樹
Chinese 乌皮石柃
Chinese 琉球黑檀

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
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zimbabwe
    • West Tropical Africa
      • Benin
      • Burkina
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000648873
KEW urn:lsid:ipni.org:names:322393-1
Open Tree Of Life 100279
NCBI Taxonomy 240001
IPNI 322393-1
iNaturalist 343774
GBIF 3032960
Freebase /m/0w7qcl_
Elurikkus 353329
Wikipedia Diospyros_ferrea
CMAUP NPO26950

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
A Review of the Potential of Poly-(lactide-co-glycolide) Nanoparticles as a Delivery System for an Active Antimycobacterial Compound, 7-Methyljuglone Diedericks B, Kok AM, Mandiwana V, Lall N Pharmaceutics 01-Feb-2024
PMCID:PMC10893214
doi:10.3390/pharmaceutics16020216
PMID:38399270
Cytotoxic Potential of Diospyros villosa Leaves and Stem Bark Extracts and Their Silver Nanoparticles Adu OT, Naidoo Y, Lin J, Dwarka D, Mellem J, Murthy HN, Dewir YH Plants (Basel) 08-Feb-2023
PMCID:PMC9967851
doi:10.3390/plants12040769
PMID:36840116
Mangrove floristic composition dataset of the Setiu Lagoon, Terengganu Malaysia Muhammad Nor SM, Sahari MS, Razali NA, Salam MR, Wan Mustaffa WF, Stephen ER, Yusof RM, Jamaludin PN, Jamaludin PN, Mokhetar N Data Brief 04-Mar-2022
PMCID:PMC8960900
doi:10.1016/j.dib.2022.108020
PMID:35360048
Plant-Based Synthesis of Gold Nanoparticles and Theranostic Applications: A Review Muddapur UM, Alshehri S, Ghoneim MM, Mahnashi MH, Alshahrani MA, Khan AA, Iqubal SM, Bahafi A, More SS, Shaikh IA, Mannasaheb BA, Othman N, Maqbul MS, Ahmad MZ Molecules 18-Feb-2022
PMCID:PMC8875495
doi:10.3390/molecules27041391
PMID:35209180
Distribution and utilization of homestead windbreak Fukugi (Garcinia subelliptica Merr.) trees: an ethnobotanical approach Chen B, Akamine H J Ethnobiol Ethnomed 22-Feb-2021
PMCID:PMC7898781
doi:10.1186/s13002-021-00434-3
PMID:33618759
A high-quality chromosomal genome assembly of Diospyros oleifera Cheng Suo Y, Sun P, Cheng H, Han W, Diao S, Li H, Mai Y, Zhao X, Li F, Fu J Gigascience 16-Jan-2020
PMCID:PMC6964648
doi:10.1093/gigascience/giz164
PMID:31944244
Complete plastome sequences of Diospyros maclurei Merr. and Diospyros hainanensis Merr. (Ebenaceae): two endemic species in Hainan Province, China Liu WW, Tan XH, Zhao KK, Zhu ZX, Wang HF Mitochondrial DNA B Resour 30-Oct-2018
PMCID:PMC7799653
doi:10.1080/23802359.2018.1524724
PMID:33474466
Phyto-assisted synthesis, characterization and applications of gold nanoparticles – A review Santhoshkumar J, Rajeshkumar S, Venkat Kumar S Biochem Biophys Rep 21-Jun-2017
PMCID:PMC5614687
doi:10.1016/j.bbrep.2017.06.004
PMID:28955767
Rinorea niccolifera (Violaceae), a new, nickel-hyperaccumulating species from Luzon Island, Philippines Fernando ES, Quimado MO, Doronila AI PhytoKeys 09-May-2014
PMCID:PMC4023331
doi:10.3897/phytokeys.37.7136
PMID:24843295
Interaction between forest biodiversity and people’s use of forest resources in Roviana, Solomon Islands: implications for biocultural conservation under socioeconomic changes Furusawa T, Sirikolo MQ, Sasaoka M, Ohtsuka R J Ethnobiol Ethnomed 27-Jan-2014
PMCID:PMC3974228
doi:10.1186/1746-4269-10-10
PMID:24468329
Nucleated succession by an endemic palm Phoenix pusilla enhances diversity of woody species in the arid Coromandel Coast of India Kinhal V, Parthasarathy N AoB Plants 21-May-2010
PMCID:PMC3000698
doi:10.1093/aobpla/plq007
PMID:22476065
Mixed-power scaling of whole-plant respiration from seedlings to giant trees Mori S, Yamaji K, Ishida A, Prokushkin SG, Masyagina OV, Hagihara A, Hoque AT, Suwa R, Osawa A, Nishizono T, Ueda T, Kinjo M, Miyagi T, Kajimoto T, Koike T, Matsuura Y, Toma T, Zyryanova OA, Abaimov AP, Awaya Y, Araki MG, Kawasaki T, Chiba Y, Umari M Proc Natl Acad Sci U S A 08-Jan-2010
PMCID:PMC2824365
doi:10.1073/pnas.0902554107
PMID:20080600
Valorizing the 'Irulas' traditional knowledge of medicinal plants in the Kodiakkarai Reserve Forest, India Ragupathy S, Newmaster SG J Ethnobiol Ethnomed 14-Apr-2009
PMCID:PMC2681454
doi:10.1186/1746-4269-5-10
PMID:19366462
The road from Santa Rosalia: A faster tempo of evolution in tropical climates Wright S, Keeling J, Gillman L Proc Natl Acad Sci U S A 03-May-2006
PMCID:PMC1472511
doi:10.1073/pnas.0510383103
PMID:16672371

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
cis-3-Hexenyl benzoate 5367706 Click to see CCC=CCCOC(=O)C1=CC=CC=C1 204.26 unknown via CMAUP database
Ethyl benzoate 7165 Click to see CCOC(=O)C1=CC=CC=C1 150.17 unknown via CMAUP database
Hexyl benzoate 23235 Click to see CCCCCCOC(=O)C1=CC=CC=C1 206.28 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 / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 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 / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see CC(=O)OCC1=CC=CC=C1 150.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2-Phenylphenol 7017 Click to see C1=CC=C(C=C1)C2=CC=CC=C2O 170.21 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 150.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown via CMAUP database
> Benzenoids / Naphthalenes
(2E)-8-hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 15082476 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=C3C=C(C4=C(C3=O)C(=CC(=C4)C)O)OC)C=C2OC 404.40 unknown https://doi.org/10.1039/P19740001128
https://doi.org/10.1039/C29700001461
https://doi.org/10.1016/S0031-9422(00)84643-9
8-Hydroxy-2-(8-hydroxy-4-methoxy-6-methyl-1-oxonaphthalen-2-ylidene)-4-methoxy-6-methylnaphthalen-1-one 140775093 Click to see CC1=CC2=C(C(=C1)O)C(=O)C(=C3C=C(C4=C(C3=O)C(=CC(=C4)C)O)OC)C=C2OC 404.40 unknown https://doi.org/10.1016/S0031-9422(00)84643-9
https://doi.org/10.1039/C29700001461
> Benzenoids / Naphthalenes / Naphthoquinones
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1016/S0031-9422(00)84643-9
Isodiospyrin 99298 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1C3=C4C(=O)C=CC(=O)C4=C(C=C3C)O)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)84643-9
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide 20488062 Click to see [H+].C1=CC=C(C=C1)[O-] 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see C1=CC(=CC=C1O)O 110.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3R)-oct-1-en-3-ol 6992244 Click to see CCCCCC(C=C)O 128.21 unknown via CMAUP database
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown via CMAUP database
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
cis-3-Hexen-1-ol 5281167 Click to see CCC=CCCO 100.16 unknown via CMAUP database
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown via CMAUP database
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown via CMAUP database
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown via CMAUP database
(+)-3-Carene 443156 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(2S)-2-[(1R)-4-methylcyclohex-3-en-1-yl]propanal 76958477 Click to see CC1=CCC(CC1)C(C)C=O 152.23 unknown via CMAUP database
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 11788398 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown via CMAUP database
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown via CMAUP database
Cuparene 86895 Click to see CC1=CC=C(C=C1)C2(CCCC2(C)C)C 202.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(4aR,6aR,6aS,8aR,12aS,14aR,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 392170 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11870460 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 162955616 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84643-9
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
https://doi.org/10.1016/S0031-9422(00)84643-9
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
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 via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,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-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97297-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl Acetate 8857 Click to see CCOC(=O)C 88.11 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
(R)-3-Hydroxy-2-oxobutanoicacid 15284009 Click to see CC(C(=O)C(=O)O)O 118.09 unknown via CMAUP database
4-Hydroxy-2-oxobutanoic acid 11963036 Click to see C(CO)C(=O)C(=O)O 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(S)-(-)-2-Methyl-1-butanol 2723602 Click to see CCC(C)CO 88.15 unknown via CMAUP database
1-Butanol 263 Click to see CCCCO 74.12 unknown via CMAUP database
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(S)-(+)-2-Pentanol 2724896 Click to see CCCC(C)O 88.15 unknown via CMAUP database
3-Methyl-3-buten-2-ol, (R)- 10678185 Click to see CC(C(=C)C)O 86.13 unknown via CMAUP database
3-Pentanol 11428 Click to see CCC(CC)O 88.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5315597 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 434.40 unknown via CMAUP database
4-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]phenol 11968602 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 434.40 unknown via CMAUP database
Pyroside 5315513 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)O)O)O)O 314.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Valeraldehyde 8063 Click to see CCCCC=O 86.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(E,Z)-2,4-heptadienal 11788274 Click to see CCC=CC=CC=O 110.15 unknown via CMAUP database
2-Decenal 5283345 Click to see CCCCCCCC=CC=O 154.25 unknown via CMAUP database
2-Heptenal 5283316 Click to see CCCCC=CC=O 112.17 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
2,4-Heptadienal 5283321 Click to see CCC=CC=CC=O 110.15 unknown via CMAUP database
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown via CMAUP database
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
Octanal 454 Click to see CCCCCCCC=O 128.21 unknown via CMAUP database
trans-2,cis-6-Nonadienal 643731 Click to see CCC=CCCC=CC=O 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Octadecanone 81844 Click to see CCCCCCCCCCCCCCCCC(=O)C 268.50 unknown via CMAUP database
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Alpha-diketones
2,3-Butanedione 650 Click to see CC(=O)C(=O)C 86.09 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
[(7S,10R,11S)-9,9-dimethyl-16-oxo-14-phenyl-5,8,13-trioxatetracyclo[10.4.0.02,6.07,11]hexadeca-1(12),2(6),3,14-tetraen-10-yl] acetate 162893780 Click to see CC(=O)OC1C2C(C3=C(C=CO3)C4=C2OC(=CC4=O)C5=CC=CC=C5)OC1(C)C 392.40 unknown https://doi.org/10.1016/S0031-9422(00)84643-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters / O-cinnamoyl glycosides
1-O-trans-Cinnamoyl-beta-D-glucopyranose 5280653 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O 310.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
Cinnamtannin B1 475277 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Cinnamtannin B2 16130973 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=C(C(=CC(=C67)O)O)C8C(C(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)O)O)C1=CC(=C(C=C1)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1153.00 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Epicatechin-(4beta->8)-epicatechin-(2beta->7,4beta->8)-catechin 10350652 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=C(C(=CC(=C45)O)O)C6C(C(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)C9=CC(=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Proanthocyanidin A1 9872976 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown via CMAUP database
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B6 474540 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B8 474541 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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 / 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
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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 11972444 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 26202188 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 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
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Hyperoside 5281643 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
Isoquercitin 10813969 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
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown via CMAUP database
Quercetin-3-o-alpha-d-arabinofuranoside 11968848 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database

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