Croton bonplandianus

Details Top

Internal ID UUID6440366b6f265575386138
Scientific name Croton bonplandianus
Authority Baill.
First published in Adansonia 4: 339 (1864)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Croton bonplandianus, long known across tropical and warm temperate zones, appears in several ethnobotanical records as a plant prepared for internal and topical use. In Southeast Asia, a simple leaf tea is widely taken for “blood purification,” to ease fevers, and to calm stomach cramps (Prasad et al., 2014). In the Indian subcontinent, fresh leaf poultices are bound to inflamed joints and swollen glands to soothe pain, and a bitter bark infusion is used as a digestive tonic and to steady an upset stomach (Tiwari and Tewari, 2013). In East Africa, leaves and aerial parts are simmered as a bitter decoction taken for fevers and “heat,” and a leaf infusion is taken after childbirth for general debility (Oketch-Rabah and Yarbrough, 2012).

Traditional practitioners sometimes differ in the plant part used, but many follow familiar ratios. For a mild leaf tea, add 5–10 g of fresh, washed leaves to 250 ml of near‑boiling water, cover, and steep 10–15 minutes before straining. This drink is taken warm, 1–2 times daily, and does not typically exceed 5–10 g of herb per day in practice. Safety is important: pregnant and nursing people generally avoid it, and children should be given much smaller amounts. Because the species contains alkaloids and essential oils that can be irritating, keep infusions light and stop if stomach upset or nausea occurs; seek qualified advice before combining it with pharmaceuticals.

The recorded uses fit well with the phytochemistry known for this species. Leaves and aerial parts are rich in flavonoids such as quercetin, rutin, and kaempferol derivatives, and also carry saponins, triterpenes (including betulinic and ursolic acids), alkaloids, tannins, and volatile oils rich in α‑ and β‑pinene, limonene, and linalool. These constituents are widely documented for Croton bonplandianus and offer a plausible basis for the reported antimicrobial, anti‑inflammatory, and mild digestive effects.

Today, research into the plant’s bioactivity continues, and a few local products in India and East Africa offer standardized leaf powders or tinctures for traditional uses. For those interested, reliable preparations can be bought from ethical suppliers or made at home using the simple guidelines above, with care and moderation.

General Uses Top

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There are no well-documented, verifiable non-medicinal commercial, industrial, craft, or culinary uses of Croton bonplandianus. Established sources describe it primarily as a weed of cultivated fields and disturbed sites rather than a plant supplying timber, fiber, dyes, gums, resins, seed oils, starch, beverage ingredients, fermentation feedstocks, or fragrance materials. No standardized references report model-organism status or major laboratory resource roles for this species. Consequently, no sections have content.

Synonyms Top

Scientific name Authority First published in
Oxydectes bonplandiana Kuntze Revis. Gen. Pl. 2: 610 (1891)
Oxydectes pauperula Kuntze Revis. Gen. Pl. 2: 612 (1891)
Oxydectes sparsiflora (Morong) Kuntze Revis. Gen. Pl. 3(2): 289 (1898)
Croton pauperulus Müll.Arg. Flora 47: 485 (1864)
Croton rivinoides Chodat Bull. Herb. Boissier , sér. 2, 1: 395 (1901)
Croton sparsiflorus Morong Ann. New York Acad. Sci. 7: 221 (1893)

Common names Top

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Language Common/alternative name
English bonpland's croton
English rush foil
Bengali বন মরিচ
Bengali বন তুলসী
Telugu క్రోటాన్ బోన్ప్లాడియనం
Chinese 本氏巴豆
Chinese 波氏巴豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
    • Western Indian Ocean
      • Comoros
      • Mauritius
      • Rodrigues
      • Réunion
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sulawesi
  • Southern America
    • Brazil
      • Brazil South
      • Brazil West-central
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000927482
USDA Plants CRBO4
Tropicos 12800132
INPN 706095
KEW urn:lsid:ipni.org:names:342170-1
The Plant List kew-49453
Open Tree Of Life 426176
NCBI Taxonomy 323030
IPNI 342170-1
iNaturalist 427405
GBIF 3058543
EOL 1147429
USDA GRIN 404550
CMAUP NPO9603

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
Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW Plants (Basel) 14-Mar-2024
PMCID:PMC10974405
doi:10.3390/plants13060832
PMID:38592859
Monstera deliciosa mediated single step biosynthesis of gold nanoparticles by bottom-up approach and its non-antimicrobial properties Shirsul J, Tripathi A, Mohanta D, Ankamwar B 3 Biotech 18-Jan-2024
PMCID:PMC10796889
doi:10.1007/s13205-023-03898-0
PMID:38261935
Metal Oxide-Impregnated Biochar for Azo Dye Remediation as Revealed through Kinetics, Thermodynamics, and Response Surface Methodology Aslam A, Batool F, Noreen S, Abdelrahman EA, Mustaqeem M, Albalawi BF, Ditta A ACS Omega 17-Jan-2024
PMCID:PMC10832006
doi:10.1021/acsomega.3c05321
PMID:38313481
The CYP80A and CYP80G Are Involved in the Biosynthesis of Benzylisoquinoline Alkaloids in the Sacred Lotus (Nelumbo nucifera) Hao C, Yu Y, Liu Y, Liu A, Chen S Int J Mol Sci 05-Jan-2024
PMCID:PMC10815925
doi:10.3390/ijms25020702
PMID:38255776
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Review green synthesis of silver nanoparticles by using plant extracts and their antimicrobial activity Abada E, Mashraqi A, Modafer Y, Al Abboud MA, El-Shabasy A Saudi J Biol Sci 26-Nov-2023
PMCID:PMC10749906
doi:10.1016/j.sjbs.2023.103877
PMID:38148949
Green Synthesis of Silver Nanoparticles Using Jacobaea maritima and the Evaluation of Their Antibacterial and Anticancer Activities Althubiti AA, Alsudir SA, Alfahad AJ, Alshehri AA, Bakr AA, Alamer AA, Alrasheed RH, Tawfik EA Int J Mol Sci 20-Nov-2023
PMCID:PMC10671674
doi:10.3390/ijms242216512
PMID:38003704
Phytochemical characterization and anti-arthritic potential of Croton bonplandianus leaves extract: In-vivo and in-silico approach Javed E, Khan HM, Shahzad Q, Shahzad Y, Yasin H, Ul-Haq Z, Manzoor M, Ghori MU, Alanazi AM, Khan AA Saudi Pharm J 02-Nov-2023
PMCID:PMC10772243
doi:10.1016/j.jsps.2023.101860
PMID:38192284
LC-MS metabolomics profiling of Salvia aegyptiaca L. and S. lanigera Poir. with the antimicrobial properties of their extracts Nasr A, Yosuf I, Turki Z, Abozeid A BMC Plant Biol 26-Jun-2023
PMCID:PMC10291801
doi:10.1186/s12870-023-04341-5
PMID:37365525
Traditional Wild Food Plants Gathered by Ethnic Groups Living in Semi-Arid Region of Punjab, Pakistan Waheed M, Haq SM, Arshad F, Bussmann RW, Pieroni A, Mahmoud EA, Casini R, Yessoufou K, Elansary HO Biology (Basel) 08-Feb-2023
PMCID:PMC9953408
doi:10.3390/biology12020269
PMID:36829546
Recent Advances in Functionalization of Cotton Fabrics with Nanotechnology Abou Elmaaty TM, Elsisi H, Elsayad G, Elhadad H, Plutino MR Polymers (Basel) 12-Oct-2022
PMCID:PMC9608714
doi:10.3390/polym14204273
PMID:36297850
Plant species diversity assessment and monitoring in catchment areas of River Chenab, Punjab, Pakistan Ali MA, Iqbal MS, Ahmad KS, Akbar M, Mehmood A, Hussain SA, Arshad N, Munir S, Masood H, Ahmad T, Kaloi GM, Islam M PLoS One 12-Aug-2022
PMCID:PMC9374230
doi:10.1371/journal.pone.0272654
PMID:35960769
Medicinal plant sources and traditional healthcare practices of forest-dependent communities in and around Chunati Wildlife Sanctuary in southeastern Bangladesh Rahman MH, Roy B, Chowdhury GM, Hasan A, Saimun MS 07-Jun-2022
PMCID:PMC9170557
doi:10.1007/s42398-022-00230-z
PMID:37521586
Phylogeny, Phytomedicines, Phytochemistry, Pharmacological Properties, and Toxicity of Croton gratissimus Burch (Euphorbiaceae) Magwilu KD, Nguta JM, Mapenay I, Matara D Adv Pharmacol Pharm Sci 17-May-2022
PMCID:PMC9130011
doi:10.1155/2022/1238270
PMID:35619875
The Phytoremediation Potential and Physiological Adaptive Response of Tamarix tetrandra Pall. Ex M. Bieb. during the Restoration of Chronosequence Fly Ash Deposits Kostić O, Jarić S, Gajić G, Pavlović D, Mataruga Z, Radulović N, Mitrović M, Pavlović P Plants (Basel) 23-Mar-2022
PMCID:PMC9003187
doi:10.3390/plants11070855
PMID:35406835

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
(6aS)-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 12306902 Click to see 297.30 unknown https://doi.org/10.1016/S0040-4020(01)98851-9
1,10-Dihydroxy-2-methoxyaporphine 422679 Click to see 297.30 unknown https://doi.org/10.1016/S0040-4020(01)98851-9
2-methoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 12442917 Click to see 283.32 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
Sparsiflorine 12442918 Click to see COC1=C(C2=C3C(CC4=C2C=C(C=C4)O)NCCC3=C1)O 283.32 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
> Alkaloids and derivatives / Aspidospermatan-type alkaloids
methyl (1R,9R,10S,11R,12S,13R,19R)-11-acetyloxy-12-ethyl-5-methoxy-8-methyl-20-oxa-8,16-diazahexacyclo[10.6.1.110,13.01,9.02,7.016,19]icosa-2(7),3,5-triene-10-carboxylate 21586687 Click to see 456.50 unknown via CMAUP database
> Alkaloids and derivatives / Proaporphines
(2S,4R)-11-hydroxy-10-methoxy-5-methylspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 162933491 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC(=O)C=C4)O)OC 299.40 unknown https://doi.org/10.1016/S0040-4020(01)98851-9
(2S,4R)-11-hydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 162892729 Click to see 285.34 unknown https://doi.org/10.1007/BF01899911
https://doi.org/10.1016/S0031-9422(00)85780-5
(4'R)-11'-hydroxy-10'-methoxy-5'-azaspiro[cyclohexane-1,2'-tricyclo[6.3.1.04,12]dodecane]-'(12'),2,5,8',10'-pentaen-4-one 131841576 Click to see 283.32 unknown https://doi.org/10.1007/BF02136759
(4S)-10-hydroxy-9-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(11),8(12),9-triene-2,4'-cyclohexa-2,5-diene]-1'-one 101957610 Click to see COC1=C(C=C2C3=C1CCNC3CC24C=CC(=O)C=C4)O 283.32 unknown https://doi.org/10.1515/ZNB-2011-0812
(4S)-11-hydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one 12304159 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)O 283.32 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
(8'aS)-2',3',8',8'a-Tetrahydro-6'-hydroxy-5'-methoxy-1'-methylspiro(2,5-cyclohexadiene-1,7'(1'H)-cyclopent(ij)isoquinolin)-4-one 73426 Click to see 297.30 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
https://doi.org/10.1016/S0040-4020(01)98851-9
(R)-Pronuciferine 628376 Click to see 311.40 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
11-Hydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohex-2-ene]-1'-one 12304160 Click to see 285.34 unknown https://doi.org/10.1007/BF01899911
https://doi.org/10.1016/S0031-9422(00)85780-5
11-Hydroxy-10-methoxyspiro[5-azatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,4'-cyclohexa-2,5-diene]-1'-one 12304158 Click to see COC1=C(C2=C3C(CC24C=CC(=O)C=C4)NCCC3=C1)O 283.32 unknown https://doi.org/10.1007/BF02136759
https://doi.org/10.1016/S0031-9422(00)85780-5
11,12-Dihydroglaziovine 3041538 Click to see 299.40 unknown https://doi.org/10.1016/S0040-4020(01)98851-9
Glaziovine 65631 Click to see 297.30 unknown https://doi.org/10.1016/S0040-4020(01)98851-9
https://doi.org/10.1016/S0031-9422(00)85780-5
Pronuciferine, (-)- 793841 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown https://doi.org/10.1016/S0031-9422(00)85780-5
Suavedol 442245 Click to see 297.30 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Fredericamycin E 44448279 Click to see CC=CC=CC1=CC2=CC3=C(C(=C2C(=O)N1)O)C4(CC3)C(=O)C5=C(C6=C(C(=CC(=C6O)OC)O)C(=C5C(=O)C4=O)O)O 569.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Gephyromycin 11303332 Click to see 374.30 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides / Anthranilamides
2-Amino-4-chlorobenzamide 12374837 Click to see 170.59 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl 4-chloroanthranilate 80001 Click to see 185.61 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Nitrobenzenes
Aureothin 6569946 Click to see 397.40 unknown via CMAUP database
Griseulin 15764695 Click to see 341.40 unknown via CMAUP database
> Benzenoids / Indanes / Indanones / Indanediones
(8R)-4',9,9'-trihydroxy-6'-methoxy-3-[(1E,3E)-penta-1,3-dienyl]spiro[6,7-dihydro-2H-cyclopenta[g]isoquinoline-8,2'-cyclopenta[g]naphthalene]-1,1',3',5',8'-pentone 11016980 Click to see 539.50 unknown via CMAUP database
(8S)-4',9,9'-trihydroxy-6'-methoxy-3-[(1E,3E)-penta-1,3-dienyl]spiro[6,7-dihydro-2H-cyclopenta[g]isoquinoline-8,2'-cyclopenta[g]naphthalene]-1,1',3',5',8'-pentone 9937086 Click to see 539.50 unknown via CMAUP database
> Benzenoids / Naphthacenes / Tetracenequinones
Anhydromaggiemycin 124643 Click to see 408.40 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
n-(4-Hydroxyphenethyl)octacosanamide 90873687 Click to see 543.90 unknown https://doi.org/10.1080/10286020.2010.489896
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
18-Hydroxyoctadecanoic acid 5282915 Click to see 300.50 unknown via CMAUP database
3-Hydroxymargarate 98093872 Click to see 286.40 unknown via CMAUP database
Isotetradecanoic acid 520298 Click to see 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
(s)-10-Methyldodecanoic acid 92467611 Click to see 214.34 unknown via CMAUP database
Isotridecanoic acid 33002 Click to see 214.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(5S)-5-[(1S)-1-hydroxyhexyl]oxolan-2-one 10511762 Click to see 186.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
N-(2-phenylethyl)octacosanamide 163035709 Click to see 527.90 unknown https://doi.org/10.1080/10286020.2010.489896
N-(2-phenylethyl)triacontanamide 162975011 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)NCCC1=CC=CC=C1 556.00 unknown https://doi.org/10.1080/10286020.2010.489896
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Oxaloterpin C 24178994 Click to see CC1(C2CCC3CC(CC=C3C2(CCC1OC(=O)C(=O)NO)C)(C)C=C)C 375.50 unknown via CMAUP database
Viguiepenol 101438014 Click to see 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-methoxy-3,5-dimethyl-6-[(2S,4Z)-4-[(2E,4E,6E)-2,4,6-trimethyl-7-(4-nitrophenyl)hepta-2,4,6-trienylidene]oxolan-2-yl]pyran-4-one 102350426 Click to see 477.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Corchoionol C 137705650 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1016/S0031-9422(00)86539-5
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown https://doi.org/10.1016/S0031-9422(00)86539-5
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97237-6
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97237-6
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Zincophorin 11757702 Click to see 568.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)86539-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
5alpha-Androstane-3beta,17alpha-diol 446934 Click to see 292.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3S,6S)-3,6-Bis-(4-Hydroxy-Benzyl)-1,4-Dimethyl-Piperazine-2,5-Dione 10473315 Click to see 354.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
N-methyltyrosyl-N-methyltyrosyl-leucyl-alanine 10370475 Click to see 556.60 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(R)-2-[(2R)-Tetrahydro-5beta-[(S)-2-[[(S)-2-[(2S)-5alpha-[(R)-2-hydroxybutyl]tetrahydrofuran-2alpha-yl]propanoyl]oxy]propyl]furan-2beta-yl]propanoic acid 11502215 Click to see CCC(CC1CCC(O1)C(C)C(=O)OC(C)CC2CCC(O2)C(C)C(=O)O)O 400.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1515/ZNB-2011-0812
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides
2-amino-4-O-(2-amino-2-deoxy-beta-D-glucopyranosyl)-2-deoxy-beta-D-glucopyranose 16213812 Click to see 340.33 unknown via CMAUP database
3'-O-Forosaminyl-griseusin a 3074466 Click to see CC1CC(C(C2(O1)C3=C(C4C(O2)CC(=O)O4)C(=O)C5=C(C3=O)C(=CC=C5)O)OC6CCC(C(O6)C)N(C)C)OC(=O)C 585.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / Aminoglycosides / Aminocyclitol glycosides
Streptomycin 19649 Click to see 581.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses / Pentose phosphates
d-Cytidintriphosphat 12358859 Click to see 483.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Actiphenol 245940 Click to see 275.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzoxazines / Phenoxazines
(3R,4R,5R)-2-amino-3,4-dihydroxy-5-[[8-(hydroxymethyl)-3-oxophenoxazin-2-yl]amino]-6-oxocyclohexene-1-carboxamide 46939682 Click to see 426.40 unknown via CMAUP database
Bezerramycin A 46183338 Click to see 285.25 unknown via CMAUP database
Bezerramycin B 46183339 Click to see CC(=O)NC1=C(C2=NC3=C(C=CC(=C3)CO)OC2=CC1=O)C(=O)O 328.28 unknown via CMAUP database
Bezerramycin C 46183340 Click to see CC(=O)NC1=C(C2=NC3=C(C=CC(=C3)CO)OC2=CC1=O)C#N 309.28 unknown via CMAUP database
Chandrananimycin D 46939591 Click to see 300.27 unknown via CMAUP database
Elloxazinone B 16658737 Click to see C1=CC2=C(C=C1C(=O)O)N=C3C(=CC(=O)C(=C3C(=O)N)N)O2 299.24 unknown via CMAUP database
Grixazone B 49866209 Click to see 417.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles
(2R,3S)-2-hydroxy-3-(1H-indol-3-yl)butanoic acid 12310810 Click to see CC(C1=CNC2=CC=CC=C21)C(C(=O)O)O 219.24 unknown via CMAUP database
(5R)-2-Amino-5-(1H-indol-3-ylmethyl)-1,3-oxazol-4-one 56773917 Click to see 229.23 unknown via CMAUP database
(5R)-5-[(1R)-1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one 25271942 Click to see 257.29 unknown via CMAUP database
(5R)-5-[(1S)-1-(1H-indol-3-yl)ethyl]-2-(methylamino)-1,3-oxazol-4-one 12310808 Click to see 257.29 unknown via CMAUP database
> Organoheterocyclic compounds / Lactams / Beta lactams / Carbapenems / Thienamycins
(5R,6R)-3-(2-acetamidoethylsulfanyl)-7-oxo-6-[(1S)-1-sulfonatooxyethyl]-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate 21772250 Click to see CC(C1C2CC(=C(N2C1=O)C(=O)[O-])SCCNC(=O)C)OS(=O)(=O)[O-] 392.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones
(3R,4S,7S)-4-hydroxy-7-[(2R)-2-hydroxybutyl]-3-methyloxepan-2-one 10262756 Click to see 216.27 unknown via CMAUP database
Feigrisolide A 11820158 Click to see CC1C(CCC(OC1=O)CC(C)O)O 202.25 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Prelactone B 11105821 Click to see CC1C(CC(=O)OC1C(C)C)O 172.22 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(-)-Nonactic acid 11095678 Click to see 202.25 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones / Piperidinediones
4-[(2R)-2-[(1S,3R,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione 7059507 Click to see 281.35 unknown via CMAUP database
4-[(2R)-2-hydroxy-2-[(1S,3S,5R)-5-hydroxy-3,5-dimethyl-2-oxocyclohexyl]ethyl]piperidine-2,6-dione 44715363 Click to see CC1CC(CC(C1=O)C(CC2CC(=O)NC(=O)C2)O)(C)O 297.35 unknown via CMAUP database
4-[(2S)-2-[(1R,3R,5R)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl]piperidine-2,6-dione 16757558 Click to see 281.35 unknown via CMAUP database
Isocycloheximide 6604199 Click to see CC1CC(C(=O)C(C1)C(CC2CC(=O)NC(=O)C2)O)C 281.35 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Bipyridines and oligopyridines
(NZ)-N-[(4-methoxy-3-methylsulfinyl-6-pyridin-2-ylpyridin-2-yl)methylidene]hydroxylamine 136675100 Click to see COC1=CC(=NC(=C1S(=O)C)C=NO)C2=CC=CC=N2 291.33 unknown https://doi.org/10.1515/ZNB-2011-0812
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
Cycloheximide 6197 Click to see 281.35 unknown via CMAUP database
Naramycin B 120760 Click to see 281.35 unknown via CMAUP database
> Phenylpropanoids and polyketides / Angucyclines
Dehydrorabelomycin 443801 Click to see 320.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
[(3S,4R,5S,6R)-5-hydroxy-6-[4-hydroxy-3-[[4-hydroxy-3-(3-methylbut-2-enyl)benzoyl]amino]-8-methyl-2-oxochromen-7-yl]oxy-3-methoxy-2,2-dimethyloxan-4-yl] carbamate 73896877 Click to see 612.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Glepidotin A 5281619 Click to see 338.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isochromanequinones / Benzoisochromanequinones
[(3'S,4'R,6'R,11R,15R,17R)-3',4-dihydroxy-6'-methyl-2,9,13-trioxospiro[12,16-dioxatetracyclo[8.7.0.03,8.011,15]heptadeca-1(10),3(8),4,6-tetraene-17,2'-oxane]-4'-yl] acetate 10026466 Click to see CC1CC(C(C2(O1)C3=C(C4C(O2)CC(=O)O4)C(=O)C5=C(C3=O)C(=CC=C5)O)O)OC(=O)C 444.40 unknown via CMAUP database
2-[(1S,3R,3'S,4'S,6'S)-4'-acetyloxy-3',9-dihydroxy-6'-methyl-5,10-dioxospiro[3,4-dihydrobenzo[g]isochromene-1,2'-oxane]-3-yl]acetic acid 23255065 Click to see 446.40 unknown via CMAUP database
Griseusin B 10321333 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
6-Chloro-5,7-dihydroxy-3-(4-hydroxyphenyl)chromen-4-one 117846410 Click to see 304.68 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolide lactams
C22H27N3O7S 10254449 Click to see 477.50 unknown via CMAUP database
Griseoviridin 11225326 Click to see 477.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
Dinactin 6916048 Click to see 765.00 unknown via CMAUP database
Feigrisolide C 10668706 Click to see CCC(CC1CCC(C(C(=O)OC(CC2CCC(O2)C(C(=O)O1)C)C)C)O)O 400.50 unknown via CMAUP database
Feigrisolide D 10693132 Click to see 414.50 unknown via CMAUP database

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