Luffa acutangula - Unknown
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Internal ID UUID643ff3f37d62c791940099
Scientific name Luffa acutangula
Authority Roxb.
First published in Hort. Bengal. 70. 1814

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Synonyms Top

Scientific name Authority First published in
Luffa umbellata M.Roem. Fam. Nat. Syn. Monogr. 2: 63 (1846)
Luffa kleinii Wight & Arn. Prodr. Fl. Ind. Orient. : 344 (1834)
Luffa tenera Royle Ill. Bot. Himal. Mts. : 219 (1835)
Luffa plukenetiana Ser. Prodr. 3: 302 (1828)
Luffa foetida Cav. Icon. 1: 7 (1791)
Luffa forskaolii Schweinf. ex Harms Repert. Spec. Nov. Regni Veg. 19: 232 (1923)
Luffa amara Roxb. Fl. Ind. ed. 1832 , 3: 715 (1832)
Luffa cattu-picinna Ser. Prodr. 3: 303 (1828)
Cucumis acutangulus L. Sp. Pl. : 1011 (1753)
Cucumis lineatus Bosc J. Hist. Nat. 2: 251 (1792)
Cucumis megacarpus G.Don Gen. Hist. 3: 28 (1834)
Cucumis operculatus Roxb. ex Wight & Arn. Prodr. Fl. Ind. Orient. : 343 (1834)
Cucurbita acutangula Blume Bijdr. Fl. Ned. Ind. : 932 (1826)
Cucurbita campanulata D.Dietr. Syn. Pl. 5: 360 (1852)
Cucurbita umbellata J.G.Klein ex Willd. Sp. Pl., ed. 4 , 4: 608 (1805)
Luffa acutangula var. forskalii (Schweinf. ex Harms) Heiser & E.E.Schill. Biotropica 123 1990
Luffa acutangula var. amara (Roxb.) C.B.Clarke Fl. Brit. India 2: 615 (1879)
Momordica tubiflora Wall. Numer. List [Wallich] n. 6749. 1832
Luffa gosa Buch.-Ham. Numer. List : n.º 6753 (1832)
Luffa drastica Mart. Syst. Mat. Med. Bras. : 81 (1843)
Luffa fluminensis M.Roem. Fam. Nat. Syn. Monogr. 2: 64 (1846)

Common names Top

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Language Common/alternative name
English sinkwa towelsponge
Assamese জিকা
bho तरोई
bjn karawila
Hindi तोरई
ht tòchon
Indonesian gambas
Indonesian oyong
Japanese トカドヘチマ
jv gambas
jv oyong
kge hurung
Kannada ಲೂಫ಼ಾ ಅಕ್ಯೂಟ್ಯಾಂಗ್ಯುಲಾ
ks تریل
mad langkèr
Macedonian остроребрена луфа
Marathi शिराळे
Marathi शिरांचा दोडका
Marathi दोडके
Marathi दोडका
Malay petola segi
Burmese ခဝဲပင်
Norwegian Bokmål kantagurk
Nepali पाटे घिरौंला
Dutch teroi
Dutch teroi luffa
Dutch vleugelkomkommer
Russian Люффа остроребристая
su oyong
Swahili dodoki
Thai บวบเหลี่ยม
Urdu ترئی
Vietnamese mướp khía
Chinese 毛草龙
Chinese 丝瓜皮
Chinese 棱角絲瓜
Chinese 丝瓜
Chinese 丝瓜叶
Chinese 丝瓜子
Chinese 丝瓜子胃
Chinese 丝瓜根
Chinese 广东丝瓜
Chinese 丝瓜络
Chinese 丝瓜花
Chinese 丝瓜蒂
Chinese 丝瓜藤
Chinese 天罗水
Chinese 稜角絲瓜
Chinese 十角絲瓜
Chinese 八角瓜
Chinese 野黄麻
Chinese 棱角丝瓜
Chinese 广东丝瓜*(棱角丝瓜)

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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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

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Database ID/link to page
World Flora Online wfo-0000358861
UNII 8B1NV4W5KR
USDA Plants LUAC2
Tropicos 9200006
INPN 448242
KEW urn:lsid:ipni.org:names:105280-3
The Plant List kew-2338862
Open Tree Of Life 565719
Observations.org 119633
NCBI Taxonomy 56866
Nature Serve 2.152925
IPNI 293059-1
iNaturalist 164869
GBIF 2874601
Freebase /m/046680n
EPPO LUFAC
EOL 487004
USDA GRIN 22787
Wikipedia Luffa_acutangula

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_036850905.1 ASM3685090v1 Chromosome South China Agricultural University 2024-02-26 10.0x 705.54 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
On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S Sci Rep 10-May-2024
PMCID:PMC11087530
doi:10.1038/s41598-024-61428-1
PMID:38730080
Risk assessment of Retithrips syriacus for the EU 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, Reignault PL, Stefani E, Thulke H, van der Werf W, Yuen J, Zappalà L, Bezerra Lima ÉF, Makowski D, Crotta M, Gobbi A, Golic D, Maiorano A, Mosbach‐Schulz O, Rossi E, Terzidou A, Vicent Civera A EFSA J 29-Apr-2024
PMCID:PMC11056851
doi:10.2903/j.efsa.2024.8741
PMID:38686341
TiO2 Nanocomposite Coatings and Inactivation of Carbapenemase-Producing Klebsiella Pneumoniae Biofilm—Opportunities and Challenges Bereanu AS, Vintilă BI, Bereanu R, Codru IR, Hașegan A, Olteanu C, Săceleanu V, Sava M Microorganisms 28-Mar-2024
PMCID:PMC11051735
doi:10.3390/microorganisms12040684
PMID:38674628
A metagenomic investigation of phytoplasma diversity in Australian vegetable growing regions Rodrigues Jardim B, Gambley C, Tran-Nguyen LT, Webster C, Kehoe M, Kinoti WM, Bond S, Davis R, Jones L, Pathania N, Sharman M, Chapman T, Rodoni BC, Constable FE Microb Genom 06-Mar-2024
PMCID:PMC10999746
doi:10.1099/mgen.0.001213
PMID:38446015
Nano-enabled agrochemicals: mitigating heavy metal toxicity and enhancing crop adaptability for sustainable crop production Ghorbani A, Emamverdian A, Pehlivan N, Zargar M, Razavi SM, Chen M J Nanobiotechnology 05-Mar-2024
PMCID:PMC10913482
doi:10.1186/s12951-024-02371-1
PMID:38443975
Identification of WRKY Family Members and Characterization of the Low-Temperature-Stress-Responsive WRKY Genes in Luffa (Luffa cylindrica L.) Liu J, Peng L, Cao C, Bai C, Wang Y, Li Z, Zhu H, Wen Q, He S Plants (Basel) 28-Feb-2024
PMCID:PMC10935285
doi:10.3390/plants13050676
PMID:38475522
Nanoencapsulation of apocynin and vanillic acid extracted from Picrorhiza kurroa Royle ex Benth plant roots and its characterisation Manasa V, Shubangi S, Jose A, Rame Gowda R, Serva Peddha M, Krishnaswamy K Heliyon 14-Feb-2024
PMCID:PMC10881362
doi:10.1016/j.heliyon.2024.e26156
PMID:38390167
Genetic Diversity and DNA Barcoding of Thrips in Bangladesh Khatun MF, Hwang HS, Kang JH, Lee KY, Kil EJ Insects 03-Feb-2024
PMCID:PMC10888972
doi:10.3390/insects15020107
PMID:38392526
The complete chloroplast genome sequence of Thladiantha nudiflora Hemsl. ex F.B.Forbes & Hemsl. 1887 (Cucurbitaceae) Zhao YY, Chen MM, Duan BL, Xie QZ, Miao Q Mitochondrial DNA B Resour 25-Jan-2024
PMCID:PMC10812858
doi:10.1080/23802359.2024.2305402
PMID:38282981
Spotlight on therapeutic efficiency of green synthesis metals and their oxide nanoparticles in periodontitis Kiarashi M, Mahamed P, Ghotbi N, Tadayonfard A, Nasiri K, Kazemi P, Badkoobeh A, Yasamineh S, Joudaki A J Nanobiotechnology 05-Jan-2024
PMCID:PMC10770920
doi:10.1186/s12951-023-02284-5
PMID:38183090
Histopathology and quantification of green fluorescent protein-tagged Fusarium oxysporum f. sp. luffae isolate in resistant and susceptible Luffa germplasm Namisy A, Chen SY, Huang JH, Unartngam J, Thanarut C, Chung WH Microbiol Spectr 04-Jan-2024
PMCID:PMC10846128
doi:10.1128/spectrum.03127-23
PMID:38174927
Characteristics and Key Features of Antimicrobial Materials and Associated Mechanisms for Diverse Applications Agarwalla A, Ahmed W, Al-Marzouqi AH, Rizvi TA, Khan M, Zaneldin E Molecules 11-Dec-2023
PMCID:PMC10745420
doi:10.3390/molecules28248041
PMID:38138531
Cucumber grafting on indigenous cucurbit landraces confers salt tolerance and improves fruit yield by enhancing morpho-physio-biochemical and ionic attributes Abbas F, Faried HN, Akhtar G, Ullah S, Javed T, Shehzad MA, Ziaf K, Razzaq K, Amin M, Wattoo FM, Hafeez A, Rahimi M, Abeed AH Sci Rep 07-Dec-2023
PMCID:PMC10709624
doi:10.1038/s41598-023-48947-z
PMID:38066051
Characterization of Sesuvium sesuvioides Using High-Performance Liquid Chromatography and Validation of Its In Vivo Anti-hyperthyroidism Effect via Suppressing Oxidative Stress and Inflammatory Markers Sajid-ur-Rehman M, Ishtiaq S, Khan MS, Jabeen Q, Youssef FS, Ahmed SA, Elhady SS, Ashour ML ACS Omega 22-Nov-2023
PMCID:PMC10701866
doi:10.1021/acsomega.3c06630
PMID:38075807
Preparation of Herbal Nano-Formulation-Assisted Mouth Paint Using Titanium Dioxide Nanoparticles and Its Biomedical Applications Rifaath M, Rajeshkumar S, Anandan J, Munuswamy T, Govindharaj S Cureus 05-Nov-2023
PMCID:PMC10698307
doi:10.7759/cureus.48332
PMID:38060706

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 101601973 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)C(=O)O)O)OC9C(C(C(CO9)O)O)O)O)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1439.50 unknown https://doi.org/10.1248/CPB.39.889
(2S,3S,4S,5R,6R)-6-[[(4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxane-2-carboxylic acid 101601974 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)C(=O)O)O)OC9C(C(C(CO9)O)O)O)O)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1439.50 unknown https://doi.org/10.1248/CPB.39.889
[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (3S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-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-carboxylate 101596470 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC5(C(=CCC6C5(CCC7C6(CCC(C7(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C3CC(C(C4)O)(C)C)C)O)O)O)O)OC1C(C(C(CO1)O)O)O 1207.30 unknown https://doi.org/10.1248/CPB.39.599
[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101596469 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)O)OC1C(C(C(CO1)O)O)O 1191.30 unknown https://doi.org/10.1248/CPB.39.599
[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101596472 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1323.50 unknown https://doi.org/10.1248/CPB.39.599
[(2S,3R,4S,5S)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101596471 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1323.50 unknown https://doi.org/10.1248/CPB.39.599
[(2S,3R,4S,5S)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101597197 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1455.60 unknown https://doi.org/10.1248/CPB.39.599
[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6S)-3-hydroxy-6-methyl-4,5-bis[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy]oxan-2-yl]oxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101596473 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(CO1)O)O)O 1323.50 unknown https://doi.org/10.1248/CPB.39.599
10-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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 3832176 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 781.00 unknown https://doi.org/10.1248/CPB.39.599
Acutoside A 21606142 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 781.00 unknown https://doi.org/10.1248/CPB.39.599
Acutoside B 3536509 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)O)OC1C(C(C(CO1)O)O)O 1191.30 unknown https://doi.org/10.1248/CPB.39.599
Acutoside C 131753039 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC5(C(=CCC6C5(CCC7C6(CCC(C7(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C3CC(C(C4)O)(C)C)C)O)O)O)O)OC1C(C(C(CO1)O)O)O 1207.30 unknown https://doi.org/10.1248/CPB.39.599
Acutoside D 4353789 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)O)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O 1323.50 unknown https://doi.org/10.1248/CPB.39.599
Acutoside F 131751146 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)C)O)O)O)OC1C(C(C(CO1)O)O)O)OC1C(C(C(CO1)O)O)O 1323.50 unknown https://doi.org/10.1248/CPB.39.599
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-Methylcytosine 65040 Click to see CC1=C(NC(=O)N=C1)N 125.13 unknown https://doi.org/10.1016/S0021-9673(01)88829-4

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