Diospyros malabarica - Unknown
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Internal ID UUID644017635a097931220819
Scientific name Diospyros malabarica
Authority (Desr.) Kostel.
First published in Allg. Med.-Pharm. Fl. 3: 1099 (1834)

Description Top

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Diospyros malabarica, also known as the gaub tree, Malabar ebony, black-and-white ebony, or pale moon ebony, is a flowering tree native to the Indian Subcontinent and South East Asia. It is a slow-growing, evergreen tree that can reach up to 35 m in height with a black trunk up to 70 cm in diameter. The tree is commonly found in lowland rainforests along rivers and streams. Its fruits are round and yellow when ripe, and the tree is known for its medicinal uses in Ayurveda. The bark and unripe fruit are used for their medicinal properties, and the leaves and fruits can also be used to dye cloth black. The wood of this tree is prized for its distinctive patterns and is sometimes used in guitar manufacturing. It is also the provincial tree of Ang Thong Province in Thailand and was mentioned in Sanskrit writings as Tinduka.

Synonyms Top

Scientific name Authority First published in
Diospyros biflora Blanco Fl. Filip. : 303 (1837)
Diospyros citrifolia Wall. ex A.DC. Prodr. 8: 285 (1844)
Diospyros glutinifera (Roxb.) Wall. Numer. List : n.º 4123 B (1831)
Diospyros glutinosa J.Koenig ex Roxb. Fl. Ind. ed. 1832 , 2: 533 (1832)
Diospyros malabarica var. siamensis (Hochr.) Phengklai Thai Forest Bull., Bot. 11: 46 (1978)
Diospyros peregrina (Gaertn.) Gürke Nat. Pflanzenfam. 4(1): 164 (1891)
Diospyros peregrina f. javanica Kosterm. Ceylon J. Sci., Biol. Sci. 12: 104 (1977)
Diospyros siamensis Hochr. Pl. Bogor. Exs. : 36 (1904)
Embryopteris gelatinifera G.Don Gen. Hist. 4: 41 (1837)
Embryopteris glutinifera Roxb. Pl. Coromandel 1: 49 (1796)
Embryopteris glutinifolia hort. ex Link Enum. Hort. Berol. Alt. 2: 433 (1822)
Embryopteris peregrina Gaertn. Fruct. Sem. Pl. 1: 145 (1788)

Common names Top

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Language Common/alternative name
Arabic خرمال مالاباري
Bengali দেশি গাব
Indonesian culiket
Japanese ベンガルガキ
Kannada ಎಬನಿ ಮರ
Malayalam black-and-white ebony
Malayalam gaub tree
Malayalam malabar ebony
Malayalam pale moon ebony
Malayalam പനച്ച
Malayalam പനഞ്ഞി
Malayalam പനച്ചി
Punjabi ਡੀਓਸਪਾਈਰੋਸ ਮਾਲਾਬਾਰੀਕਾ
Tamil தும்பிலி மரம்
Thai มะพลับ
Thai ต้นมะพลับ
Chinese 法国柿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000649282
Tropicos 100324768
KEW urn:lsid:ipni.org:names:322658-1
The Plant List kew-2770098
Open Tree Of Life 1049036
NCBI Taxonomy 413755
IPNI 322658-1
iNaturalist 427523
GBIF 7295796
Freebase /m/0h53bzb
EPPO DOSMA
USDA GRIN 14299
Wikipedia Diospyros_malabarica
CMAUP NPO12233

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
Biosynthesis, characterization and study of the application of silver nanoparticle for 4-nitrophenol reduction, and antimicrobial activities Mulu M, Tefera M, Guadie A, Basavaiah K Biotechnol Rep (Amst) 21-Mar-2024
PMCID:PMC10999826
doi:10.1016/j.btre.2024.e00838
PMID:38590717
Biogenic Silver Nanoparticles for Targeted Cancer Therapy and Enhancing Photodynamic Therapy Kah G, Chandran R, Abrahamse H Cells 07-Aug-2023
PMCID:PMC10417642
doi:10.3390/cells12152012
PMID:37566091
Single botanical drugs in the Ayurvedic Pharmacopoeia of India—A quantitative ethnobotanical analysis Yao R, Heinrich M, Zhang B, Wei X, Qi Y, Gao W Front Pharmacol 11-May-2023
PMCID:PMC10213908
doi:10.3389/fphar.2023.1136446
PMID:37251315
Antidiabetic Potential of Commonly Available Fruit Plants in Bangladesh: Updates on Prospective Phytochemicals and Their Reported MoAs Alam S, Dhar A, Hasan M, Richi FT, Emon NU, Aziz MA, Mamun AA, Chowdhury MN, Hossain MJ, Kim JK, Kim B, Hasib MS, Zihad SM, Haque MR, Mohamed IN, Rashid MA Molecules 08-Dec-2022
PMCID:PMC9782115
doi:10.3390/molecules27248709
PMID:36557843
Pharmacodynamic appraisal of wound-healing herbs of Sushruta Samhita Kumar V, Nesari TM, Ghildiyal S, Sherkhane R Ayu 07-Dec-2022
PMCID:PMC9893898
doi:10.4103/ayu.AYU_34_20
PMID:36743272
A Comparative Study of Diospyros malabarica (Gaub) Extracts in Various Polarity-Dependent Solvents for Evaluation of Phytoconstituents and Biological Activities Zreen Z, Hameed A, Kiran S, Farooq T, Zaroog MS Biomed Res Int 25-Jun-2022
PMCID:PMC9250437
doi:10.1155/2022/4746223
PMID:35789643
A Critical Review of the Antimicrobial and Antibiofilm Activities of Green-Synthesized Plant-Based Metallic Nanoparticles Luzala MM, Muanga CK, Kyana J, Safari JB, Zola EN, Mbusa GV, Nuapia YB, Liesse JM, Nkanga CI, Krause RW, Balčiūnaitienė A, Memvanga PB Nanomaterials (Basel) 27-May-2022
PMCID:PMC9182092
doi:10.3390/nano12111841
PMID:35683697
Nonlinear molecular dynamics of quercetin in Gynocardia odorata and Diospyros malabarica fruits: Its mechanistic role in hepatoprotection Ghosh A, Sarmah P, Patel H, Mukerjee N, Mishra R, Alkahtani S, Varma RS, Baishya D PLoS One 21-Mar-2022
PMCID:PMC8936497
doi:10.1371/journal.pone.0263917
PMID:35313329
Global Perspective of Plant-Based Cosmetic Industry and Possible Contribution of Sri Lanka to the Development of Herbal Cosmetics Nadeeshani Dilhara Gamage DG, Dharmadasa RM, Chandana Abeysinghe D, Saman Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 04-Mar-2022
PMCID:PMC8916882
doi:10.1155/2022/9940548
PMID:35280508
Bacterial Skin Infections in Livestock and Plant-Based Alternatives to Their Antibiotic Treatment Mala L, Lalouckova K, Skrivanova E Animals (Basel) 23-Aug-2021
PMCID:PMC8388705
doi:10.3390/ani11082473
PMID:34438930
Green Synthesis of Silver Nanoparticles Using Diospyros malabarica Fruit Extract and Assessments of Their Antimicrobial, Anticancer and Catalytic Reduction of 4-Nitrophenol (4-NP) Bharadwaj KK, Rabha B, Pati S, Choudhury BK, Sarkar T, Gogoi SK, Kakati N, Baishya D, Kari ZA, Edinur HA Nanomaterials (Basel) 04-Aug-2021
PMCID:PMC8401075
doi:10.3390/nano11081999
PMID:34443829
Ethnopharmacological Survey on Medicinal Plants Used for Cosmetic Treatments in Traditional and Ayurveda Systems of Medicine in Sri Lanka Gamage DG, Dharmadasa RM, Abeysinghe DC, Wijesekara RG, Prathapasinghe GA, Someya T Evid Based Complement Alternat Med 26-Jun-2021
PMCID:PMC8257331
doi:10.1155/2021/5599654
PMID:34257686
Evolution of the adaptogenic concept from traditional use to medical systems: Pharmacology of stress‐ and aging‐related diseases Panossian AG, Efferth T, Shikov AN, Pozharitskaya ON, Kuchta K, Mukherjee PK, Banerjee S, Heinrich M, Wu W, Guo D, Wagner H Med Res Rev 25-Oct-2020
PMCID:PMC7756641
doi:10.1002/med.21743
PMID:33103257
Chemotherapeutic Potential of Carthamus Oxycantha Root Extract as Antidiarrheal and In Vitro Antibacterial Activities Ikram M, Magdy Beshbishy A, Kifayatullah M, Olukanni A, Zahoor M, Naeem M, Amin M, Shah M, Abdelaziz AS, Ullah R, Mothana RA, Siddiqui NA, Batiha GE Antibiotics (Basel) 01-May-2020
PMCID:PMC7277192
doi:10.3390/antibiotics9050226
PMID:32370087
Taxonomy and phylogeny of cercosporoid ascomycetes on Diospyros spp. with special emphasis on Pseudocercospora spp. Braun U, Nakashima C, Bakhshi M, Zare R, Shin HD, Alves RF, Sposito MB Fungal Syst Evol 03-Apr-2020
PMCID:PMC7453130
doi:10.3114/fuse.2020.06.06
PMID:32904397

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Aporphines
(6aR)-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-ol 92169951 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC)C 356.40 unknown via CMAUP database
(6aR)-2,10-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-1,11-diol 929259 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown via CMAUP database
CID 12305611 12305611 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC)C 342.40 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 https://doi.org/10.1016/S0031-9422(00)97175-9
> Benzenoids / Phenols / Methoxyphenols
3,4-Dimethoxy-5-hydroxybenzaldehyde 141513 Click to see COC1=CC(=CC(=C1OC)O)C=O 182.17 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1016/S0031-9422(00)97175-9
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(1R,3aS,4S,6aS)-4-(1,3-Benzodioxol-5-yl)tetrahydro-1H,3H-furo[3,4-c]furan-1-yl]-2-methoxyphenol 44144290 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
4-[(3R,3aS,6R,6aS)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 70695728 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenol 5315338 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Piperitol 10247670 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Pluviatilol 70695727 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Prenylpiperitol 91884985 Click to see CC(=CCOC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC)C 424.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(2S)-2alpha-(3-Methoxy-4-hydroxyphenyl)-4alpha-(1,3-benzodioxole-5-ylmethyl)tetrahydrofuran-3beta-methanol 101904398 Click to see COC1=C(C=CC(=C1)C2C(C(CO2)CC3=CC4=C(C=C3)OCO4)CO)O 358.40 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 / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
Turpinionoside B 101165165 Click to see CC1CC(CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C)O 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1016/S0031-9422(00)97175-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(7S)-7-hydroxynonadecan-2-one 162914697 Click to see CCCCCCCCCCCCC(CCCCC(=O)C)O 298.50 unknown https://doi.org/10.1016/S0031-9422(00)83935-7
Nonadecan-7-ol-2-on 129650836 Click to see CCCCCCCCCCCCC(CCCCC(=O)C)O 298.50 unknown https://doi.org/10.1016/S0031-9422(00)83935-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
alpha-Sanshool 6440935 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
beta-Sanshool 6506170 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
gamma-Sanshool 6440615 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)C 273.40 unknown via CMAUP database
Hydroxy-alpha-sanshool 10084135 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
Hydroxy-Beta-Sanshool 10220912 Click to see CC=CC=CC=CCCC=CC(=O)NCC(C)(C)O 263.37 unknown via CMAUP database
N-Isobutyl-2,4,8,10,12-tetradecapentaenamide 5318518 Click to see CC=CC=CC=CCCC=CC=CC(=O)NCC(C)C 273.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
(R)-(+)-Citronellic acid 6999957 Click to see CC(CCC=C(C)C)CC(=O)O 170.25 unknown via CMAUP database
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,4S,5R)-4-hydroxy-4-[(E,3R)-3-hydroxybut-1-enyl]-3,3,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 21630913 Click to see CC1CC(CC(C1(C=CC(C)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 390.50 unknown via CMAUP database
[(S)-3,7-Dimethyl-6-octenyl]beta-D-glucopyranoside 101854158 Click to see CC(CCC=C(C)C)CCOC1C(C(C(C(O1)CO)O)O)O 318.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-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 12358881 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)97175-9
(1R,3aR,5aS,5bR,7aR,9R,11aR,11bR,13aS,13bR)-5a-(hydroxymethyl)-3a,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 11744095 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)90674-5
(4aR,6aS,6bR,8aR,11R,12S,12aR,14bS)-4,4,6a,6b,8a,11,12,14b-octamethyl-1,2,4a,5,6,7,8,9,10,11,12,12a-dodecahydropicen-3-one 22296838 Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C 422.70 unknown https://doi.org/10.1016/S0031-9422(97)01020-0
3beta-20(29)-Lupene-3,27-diol 73082705 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)CO)C)(C)C)O)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)90674-5
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)97175-9
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)97175-9
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)97175-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-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 162965363 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)97175-9
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/10.1016/S0031-9422(00)97175-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(3S,6S)-2,2,6-Trimethyl-6-vinyltetrahydro-2H-pyran-3-yl]beta-D-glucopyranoside 101093957 Click to see CC1(C(CCC(O1)(C)C=C)OC2C(C(C(C(O2)CO)O)O)O)C 332.39 unknown via CMAUP database
1-Methyl-1-[(2R,5S)-5-methyl-5-vinyltetrahydrofuran-2-yl]ethyl beta-D-glucopyranoside 101093955 Click to see CC1(CCC(O1)C(C)(C)OC2C(C(C(C(O2)CO)O)O)O)C=C 332.39 unknown via CMAUP database
2-Methylpropyl 6-O-D-apio-beta-D-furanosyl-beta-D-glucopyranoside 101109242 Click to see CC(C)COC1C(C(C(C(O1)COC2C(C(CO2)(CO)O)O)O)O)O 368.38 unknown via CMAUP database
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see CC(=O)C1=C(C=C(C=C1OC)OC)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Piperonylic acid 7196 Click to see C1OC2=C(O1)C=C(C=C2)C(=O)O 166.13 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
7,8-Dimethoxyfuro[2,3-b]quinoline 71089525 Click to see COC1=C(C2=NC3=C(C=CO3)C=C2C=C1)OC 229.23 unknown via CMAUP database
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database

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