Jatropha integerrima

Details Top

Internal ID UUID643fdfe38f0ab297697981
Scientific name Jatropha integerrima
Authority Jacq.
First published in Enum. Syst. Pl. : 32 (1763)

Ethnobotanical Use Top

Suggest a correction!
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.

Jatropha integerrima (Jacq.) is cultivated widely as an ornamental street tree and hedge shrub in tropical and subtropical regions (Popenoe, 1974; Liogier, 1990). There is no direct, verifiable documentation of its use in infusions, decoctions, tinctures, macerations, or poultices in the ethnobotanical literature reviewed for this species. Occasional references to “Jatropha” in ethnobotanical records generally refer to other taxa (for example Jatropha curcas) and do not concern J. integerrima (Bennett et al., 2021; van Andel & Havinga, 2008). As a result, no reliable evidence supports traditional tea, tincture, or poultice preparations of J. integerrima.

General Uses Top

Suggest a correction!

Common products:
Ornamental horticulture: cultivated in subtropical and tropical landscapes for landscape and street planting; also in containers and as a bonsai subject.

Industrial and craft applications:
No established non-medicinal industrial uses are documented for this species.

Food and beverages (non-medicinal):
No documented edible uses; seeds and other plant parts contain phorbol esters and are unsuitable for food.

Colorants and tanning:
No documented dye, tannin, or pigment uses are documented.

Wood and fiber:
No documented timber or fiber uses are documented.

Fragrance and cosmetics:
No documented fragrance or cosmetic uses are documented.

Properties relevant to use:
Ornamental habit is evergreen with reddish flowers; suits small-tree/shrub form in horticulture.

Standards and regulation:
No specific standards or regulatory frameworks are documented for products derived from this species.

Sustainability and sourcing:
Widely cultivated as an ornamental; seeds are reported to be toxic and should not be collected for food or feed.

Synonyms Top

Scientific name Authority First published in
Jatropha acuminata Desr. Encycl. 4: 8 (1797)
Jatropha coccinea Hort.Cels ex Link Enum. Hort. Berol. Alt. 2: 406. 1822 [Jan-Jun 1822]
Jatropha diversifolia A.Rich. Hist. Fis. Cuba, Bot. 11: 207 (1850)
Jatropha diversifolia var. pandurifolia M.Gómez Anales Soc. Esp. Hist. Nat. 23: 51 (1894)
Jatropha hastata Jacq. Select. Stirp. Amer. Hist. : 256 (1763)
Jatropha integerrima var. coccinea (Link) N.P.Balakr. Bull. Bot. Surv. India 22: 176 (1980 publ. 1982)
Jatropha integerrima var. hastata (Jacq.) Fosberg Rhodora 78(813): 102 (1976)
Jatropha integerrima var. latifolia (Pax) N.P.Balakr. Bull. Bot. Surv. India 22: 176 (1980 publ. 1982)
Jatropha moluensis Sessé & Moc. Fl. Mexic. , ed. 2: 224 (1894)
Jatropha pandurifolia Andrews Bot. Repos. 4: t. 267 (1802)
Jatropha pandurifolia var. coccinea Pax Pflanzenr. , IV, 147, I: 50 (1910)
Jatropha pandurifolia var. latifolia Pax Pflanzenr. , IV, 147, I: 50 (1910)
Adenoropium hastatum Britton & P.Wilson Sci. Surv. Porto Rico & Virgin Islands 5: 485 (1924)
Adenoropium integerrimum (Jacq.) Pohl Pl. Bras. Icon. Descr. 1: 14 (1826)
Adenoropium pandurifolium (Andrews) Pohl Pl. Bras. Icon. Descr. 1: 14 (1826)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English spicy jatropha
English peregrina
Arabic جتروفة
Arabic يطروفة كاملة
Azerbaijani jatropha hastata
Bengali সুগন্ধি জয়তী
Bengali দিনফোটা জয়তী
Finnish karibianjatropa
French Épicar
French médicinier-guitare
Hebrew יתרופית תמימה
Indonesian bunga batavia
Indonesian peregrina
Indonesian bunga betawi
Japanese テイキンザクラ
Russian Ятрофа цельнокрайняя
Russian Ятрофа гитаролистная
Thai ปัตตาเวีย
Tonga fiki kulamūmū
Vietnamese dầu lai lá đơn
Chinese 变叶珊瑚花
Chinese 琴叶珊瑚
Chinese 變葉珊瑚花

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
      • Bangladesh
      • India
    • Malesia
      • Jawa
      • Philippines
      • Sulawesi
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Marquesas
      • Society Islands
    • Southwestern Pacific
      • Vanuatu
  • Southern America
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000219712
Florida Plant Atlas 1714
USDA Plants JAIN
Tropicos 12802176
INPN 448391
KEW urn:lsid:ipni.org:names:350290-1
The Plant List kew-104678
Plantarium 48990
Open Tree Of Life 607939
NCBI Taxonomy 316874
Nature Serve 2.138583
IPNI 350290-1
iNaturalist 164240
GBIF 3073017
Freebase /m/04f2jwx
EPPO IATIN
EOL 1156079
USDA GRIN 312795
Wikipedia Jatropha_integerrima

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
The paradox of plant preference: The malaria vectors Anopheles gambiae and Anopheles coluzzii select suboptimal food sources for their survival and reproduction Paré PS, Hien DF, Youba M, Yerbanga RS, Cohuet A, Gouagna L, Diabaté A, Ignell R, Dabiré RK, Gnankiné O, Lefèvre T Ecol Evol 25-Mar-2024
PMCID:PMC10963300
doi:10.1002/ece3.11187
PMID:38533352
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
Biosynthesis, Characterization, and Biomedical Applications of Gold Nanoparticles with Cucurbita moschata Duchesne Ex Poiret Peel Aqueous Extracts Kaval U, Hoşgören H Molecules 20-Feb-2024
PMCID:PMC10935381
doi:10.3390/molecules29050923
PMID:38474434
Unveiling the Potential of Bioinoculants and Nanoparticles in Sustainable Agriculture for Enhanced Plant Growth and Food Security Karnwal A, Dohroo A, Malik T Biomed Res Int 29-Nov-2023
PMCID:PMC10699995
doi:10.1155/2023/6911851
PMID:38075309
In vitro antimalarial activity of Syzygium cumini fruit fraction Maslachah L, Purwitasari N Open Vet J 30-Sep-2023
PMCID:PMC10576581
doi:10.5455/OVJ.2023.v13.i9.7
PMID:37842099
Detailed Metabolic Characterization of Flowers and Hips of Rosa gallica L. Grown in Open Nature Kunc N, Hudina M, Mikulič-Petkovšek M, Bavcon J, Ravnjak B, Osterc G Plants (Basel) 18-Aug-2023
PMCID:PMC10457908
doi:10.3390/plants12162979
PMID:37631190
Cyclic Peptides with Antifungal Properties Derived from Bacteria, Fungi, Plants, and Synthetic Sources Helmy NM, Parang K Pharmaceuticals (Basel) 18-Jun-2023
PMCID:PMC10301978
doi:10.3390/ph16060892
PMID:37375840
Facile Synthesis and Characterization of Chitosan Functionalized Silver Nanoparticles for Antibacterial and Anti-Lung Cancer Applications Bharathi D, Thiruvengadam Nandagopal JG, Lee J, Ranjithkumar R Polymers (Basel) 16-Jun-2023
PMCID:PMC10301133
doi:10.3390/polym15122700
PMID:37376346
Pest categorisation of Paracoccus marginatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Mar-2023
PMCID:PMC10064853
doi:10.2903/j.efsa.2023.7899
PMID:37009439
Biosynthesis of Nanoparticles Using Plant Extracts and Essential Oils Antunes Filho S, dos Santos MS, dos Santos OA, Backx BP, Soran ML, Opriş O, Lung I, Stegarescu A, Bououdina M Molecules 29-Mar-2023
PMCID:PMC10095647
doi:10.3390/molecules28073060
PMID:37049821
The Investigation of the Chemical Composition and Applicability of Gold Nanoparticles Synthesized with Amygdalus communis (Almond) Leaf Aqueous Extract as Antimicrobial and Anticancer Agents Baran MF, Keskin C, Baran A, Eftekhari A, Omarova S, Khalilov R, Adican MT, Rosić G, Selakovic D, Yıldıztekin M, Kurt K, Aytuğ Ava C, Atalar MN Molecules 07-Mar-2023
PMCID:PMC10051629
doi:10.3390/molecules28062428
PMID:36985400
Valorization of Wild Edible Plants as Food Ingredients and Their Economic Value Clemente-Villalba J, Burló F, Hernández F, Carbonell-Barrachina ÁA Foods 27-Feb-2023
PMCID:PMC10001278
doi:10.3390/foods12051012
PMID:36900530
Pest categorisation of Nipaecoccus viridis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 18-Jan-2023
PMCID:PMC9846308
doi:10.2903/j.efsa.2023.7770
PMID:36698490
Annulations involving 1-indanones to access fused- and spiro frameworks Das S, Dutta A RSC Adv 22-Nov-2022
PMCID:PMC9679735
doi:10.1039/d2ra06635a
PMID:36425193
Antimalarial Activity of Extract and Fractions of Sauropus androgynus (L.) Merr. Ekasari W, Fatmawati D, Khoiriah SM, Baqiuddin WA, Nisa HQ, Maharupini AA, Wahyuni TS, Oktarina RD, Suhartono E, Sahu RK Scientifica (Cairo) 08-Sep-2022
PMCID:PMC9477630
doi:10.1155/2022/3552491
PMID:36119646

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 / Indanes / Indanones
(4R,10R,12S)-7-hydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trien-3-one 14059527 Click to see 296.40 unknown https://doi.org/10.1021/NP900342B
(4S,10S,12S)-7-hydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trien-3-one 162949975 Click to see 296.40 unknown https://doi.org/10.1021/NP900342B
2alpha-Hydroxyjatropholone 44604948 Click to see 312.40 unknown https://doi.org/10.1021/NP900342B
2beta-Hydroxyjatropholone 44604949 Click to see CC1=C2C3C(C3(C)C)CCC(=C)C2=C4C(=C1O)CC(C4=O)(C)O 312.40 unknown https://doi.org/10.1021/NP900342B
4,7-Dihydroxy-4,8,11,11-tetramethyl-15-methylidenetetracyclo[7.6.0.02,6.010,12]pentadeca-1,6,8-trien-3-one 75079691 Click to see 312.40 unknown https://doi.org/10.1021/NP900342B
9-Hydroxy-2,7,7,8-tetramethyl-4-methylidene-1,2,4,5,6,6a,7,7a-octahydro-3H-cyclopropa[3,4]cyclohepta[1,2-e]inden-3-one 3035352 Click to see CC1CC2=C(C(=C3C4C(C4(C)C)CCC(=C)C3=C2C1=O)C)O 296.40 unknown https://doi.org/10.1021/NP900342B
Jatropholone 324064 Click to see 296.40 unknown https://doi.org/10.1021/NP900342B
Jatropholone A 14059526 Click to see CC1CC2=C(C(=C3C4C(C4(C)C)CCC(=C)C3=C2C1=O)C)O 296.40 unknown https://doi.org/10.1021/NP900342B
Jatropholone A 46881274 Click to see 296.40 unknown https://doi.org/10.1021/NP900342B
Jatropholone B 46881275 Click to see 296.40 unknown https://doi.org/10.1021/NP900342B
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2,5,11-Trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl) acetate 73808286 Click to see CC1CC2C(=CC(C(=O)CC(C=CC(C2=O)C)C(=C)C)C)C1OC(=O)C 358.50 unknown https://doi.org/10.1016/S0040-4039(03)00704-4
[(2R,3R,3aE,5R,8R,9Z,11R,12aS)-2,5,11-trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl] acetate 21590076 Click to see 358.50 unknown https://doi.org/10.1016/S0040-4039(03)00704-4
[(3aE,9Z)-2,5,11-trimethyl-6,12-dioxo-8-prop-1-en-2-yl-1,2,3,5,7,8,11,12a-octahydrocyclopenta[11]annulen-3-yl] acetate 101239631 Click to see 358.50 unknown https://doi.org/10.1002/CHIN.200332120
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Rhamnofolane and daphnane diterpenoids
(1R,4S,7R,8R,13R,14R,16S)-13-hydroxy-10,14-dimethyl-7-prop-1-en-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 162897390 Click to see 344.40 unknown https://doi.org/10.1021/NP900342B
(1R,4S,7S,8R,13S,14S,16R)-13-hydroxy-10,14-dimethyl-7-prop-1-en-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 21590078 Click to see 344.40 unknown https://doi.org/10.1016/S0040-4039(03)00704-4
(1R,4S,7S,8S,13S,14S,16R)-13-hydroxy-10,14-dimethyl-7-prop-1-en-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 162897389 Click to see CC1C(C2=C3C14OCC5(C3C(C=C(C2=O)C)C(CC5)C(=C)C)OO4)O 344.40 unknown https://doi.org/10.1021/NP900342B
(1S,4R,7S,8R,13S,14R,16R)-13-hydroxy-10,14-dimethyl-7-prop-1-en-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 21590077 Click to see CC1C(C2=C3C14OCC5(C3C(C=C(C2=O)C)C(CC5)C(=C)C)OO4)O 344.40 unknown https://doi.org/10.1016/S0040-4039(03)00704-4
(1S,4R,7S,8R,13S,14S,16R)-13-hydroxy-10,14-dimethyl-7-prop-1-en-2-yl-2,3,18-trioxapentacyclo[6.6.2.21,4.04,16.012,15]octadeca-9,12(15)-dien-11-one 101239632 Click to see 344.40 unknown https://doi.org/10.1021/NP900342B
https://doi.org/10.1002/CHIN.200332120
https://doi.org/10.1016/S0040-4039(03)00704-4
(2S,3S,6aS,7R,10aR)-2,3-dihydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydrobenzo[h]azulene-1,4-dione 44604950 Click to see 328.40 unknown https://doi.org/10.1021/NP900342B
2,3-Dihydroxy-2,5-dimethyl-10-methylidene-7-prop-1-en-2-yl-3,6a,7,8,9,10a-hexahydrobenzo[h]azulene-1,4-dione 75079692 Click to see 328.40 unknown https://doi.org/10.1021/NP900342B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,5R,8R)-3-hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-2,4,5,6,7,8-hexahydroazulen-1-one 101700054 Click to see CC1CCC(CC2=C1C(=O)CC2(C)O)C(=C)C 234.33 unknown https://doi.org/10.1021/NP900342B
3-Hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-2,4,5,6,7,8-hexahydroazulen-1-one 142602360 Click to see CC1CCC(CC2=C1C(=O)CC2(C)O)C(=C)C 234.33 unknown https://doi.org/10.1021/NP900342B
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3aS,5R,8R,8aS)-3a-hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydroazulen-1-one 44604951 Click to see 234.33 unknown https://doi.org/10.1021/NP900342B
(3aS,5R,8S,8aS)-3a-hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydroazulen-1-one 162872429 Click to see CC1CCC(CC2(C1C(=O)C=C2C)O)C(=C)C 234.33 unknown https://doi.org/10.1021/NP900342B
(5R,8S,8aR)-8a-hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-1,4,5,6,7,8-hexahydroazulen-2-one 162872689 Click to see 234.33 unknown https://doi.org/10.1021/NP900342B
3a-Hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydroazulen-1-one 75079693 Click to see 234.33 unknown https://doi.org/10.1021/NP900342B
8a-Hydroxy-3,8-dimethyl-5-prop-1-en-2-yl-1,4,5,6,7,8-hexahydroazulen-2-one 75072140 Click to see 234.33 unknown https://doi.org/10.1021/NP900342B
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,14S,19S,22S)-11-methoxy-16,22-dimethyl-19-prop-1-en-2-yl-2,5,13-trioxapentacyclo[12.8.0.01,17.03,12.04,9]docosa-3,7,9,11,16-pentaen-6-one 44604952 Click to see CC1CCC(CC2=C(CC3C12OC4=C5C(=CC(=C4O3)OC)C=CC(=O)O5)C)C(=C)C 408.50 unknown https://doi.org/10.1021/NP900342B
11-Methoxy-16,22-dimethyl-19-prop-1-en-2-yl-2,5,13-trioxapentacyclo[12.8.0.01,17.03,12.04,9]docosa-3,7,9,11,16-pentaen-6-one 75079694 Click to see 408.50 unknown https://doi.org/10.1021/NP900342B
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8S,9S,10R,11R,13R,14S,15R,17R)-11,15-dihydroxy-17-[(2R,5R)-5-(2-hydroxyethyl)-6-methylheptan-2-yl]-10,13-dimethyl-7-oxo-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 101277410 Click to see CC(C)C(CCC(C)C1CC(C2C1(CC(C3C2C(=O)C=C4C3(CCC(C4)OC(=O)C)C)O)C)O)CCO 518.70 unknown https://doi.org/10.1016/S0040-4039(03)00704-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(6R,8S,9S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 154496064 Click to see 428.70 unknown https://doi.org/10.1021/NP900342B
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
cyclo[DL-Ala-DL-Leu-DL-Leu-DL-Val-DL-Ser-DL-Pro-DL-Trp] 73228844 Click to see 766.90 unknown https://doi.org/10.1021/NP0602012
cyclo[Gly-DL-Leu-DL-Leu-DL-Leu-DL-xiThr-DL-Pro-DL-Trp] 73240787 Click to see 781.00 unknown https://doi.org/10.1021/NP0602012
cyclo[Gly-Leu-Leu-Leu-aThr-Pro-Trp] 163194220 Click to see 781.00 unknown https://doi.org/10.1021/NP0602012
Integerrimide A 16091570 Click to see 781.00 unknown https://doi.org/10.1021/NP0602012
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
cyclo[Ala-Leu-Leu-Val-Ser-Pro-D-Trp] 25093024 Click to see 766.90 unknown https://doi.org/10.1021/NP0602012
cyclo[Gly-Leu-Leu-Leu-Ser-Pro-Trp] 163103713 Click to see CC(C)CC1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N2CCCC2C(=O)NC(C(=O)NCC(=O)N1)CC3=CNC4=CC=CC=C43)CO)CC(C)C)CC(C)C 766.90 unknown https://doi.org/10.1021/NP0602012
Integerrimide B 16059804 Click to see 766.90 unknown https://doi.org/10.1021/NP0602012
> Organoheterocyclic compounds / Oxanes
(1R,2Z,6R,10S,12S,14R,15S)-3,7,7,10,14-pentamethyl-16-oxatetracyclo[10.4.0.01,15.06,10]hexadec-2-ene-4,9,11-trione 12116937 Click to see 330.40 unknown https://doi.org/10.1021/NP900342B
3,7,7,10,14-Pentamethyl-16-oxatetracyclo[10.4.0.01,15.06,10]hexadec-2-ene-4,9,11-trione 78410710 Click to see 330.40 unknown https://doi.org/10.1021/NP900342B
Citlalitrione 6449926 Click to see 330.40 unknown https://doi.org/10.1021/NP900342B

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.