PlantaeDB Logo
Login Sign-up

Ocimum americanum

Ocimum americanum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fe4c09e12f781269562
Scientific name Ocimum americanum
Authority L.
First published in Cent. Pl. I : 15 (1755)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Ocimum album Roxb. Fl. Ind. ed. 1832 , 3: 15 (1832)
Ocimum brachiatum Blume Bijdr. Fl. Ned. Ind. : 833 (1826)
Ocimum canum Sims Bot. Mag. 51: t. 2452 (1823)
Ocimum dichotomum Hochst. ex Benth. Prodr. 12: 39 (1848)
Ocimum dinteri Briq. Bull. Herb. Boissier , sér. 2, 3: 980 (1903)
Ocimum fluminense Vell. Fl. Flumin. 4: t. 11 (1829)
Ocimum fruticulosum Burch. Trav. S. Africa 2: 264 (1824)
Ocimum hispidulum Schumach. & Thonn. Beskr. Guin. Pl. : 266 (1827)
Ocimum incanescens Mart. Reise Bras. 2: 799 (1828)
Ocimum serpyllifolium var. glabrior Benth. Comm. Pl. Afr. Austr. 226 1837
Ocimum stamineum Sims Bot. Mag. 51: t. 2452 (1823)
Ocimum thymoides Baker Fl. Trop. Afr. 5: 344 (1900)
Becium obovatum var. glabrior (Benth.) Cufod. Senckenberg. Biol. 43: 287 1962
Ocimum canum var. integrifolium Engl. Bot. Jahrb. Syst. 10: 267. 1888

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English american basil
English hoary basil
English lime basil
English hransvaal basil
English hairy basil
Afrikaans wilde basielkruid
Afrikaans transvaal basielkruid
Afrikaans bostee
Afrikaans boesmansboegoe
Arabic حبق أمريكي
ban kecarum
German amerikanisches basilikum
Hausa cwai ɗwaiya
Hindi अरण्यतुलसी
Croatian limunski bosiljak
Italian basilico americano
Korean 회바질
Malay pokok kemangi
pap yerba di hole
Polish bazylia amerykańska
Portuguese alfavaca-do-campo
Kinyarwanda isonga
Tamil கஞ்சங்குல்லை
Tamil நாய்த்துளசி
Tamil புனத்துளசி
Tamil குல்லை
Telugu వన తులసి
Chinese 灰罗勒
Chinese 草灵脂
Chinese 灰羅勒

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Caprivi Strip
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
  • Southern America
    • Brazil
      • Brazil Northeast
    • Caribbean
      • Netherlands Antilles
      • Trinidad-Tobago
      • Venezuelan Antilles
    • Central America
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000253211
UNII 0899QOA7PA
Tropicos 17607555
INPN 109795
KEW urn:lsid:ipni.org:names:316218-2
The Plant List kew-136802
Open Tree Of Life 782165
Observations.org 198800
NCBI Taxonomy 204141
IPNI 316218-2
iNaturalist 181061
GBIF 2927097
Freebase /m/04y6p9l
EPPO OCICA
EOL 483863
Elurikkus 648995
USDA GRIN 402305
Wikipedia Ocimum_americanum

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
Impact of Heavy Metal Pollution in the Environment on the Metabolic Profile of Medicinal Plants and Their Therapeutic Potential Asiminicesei DM, Fertu DI, Gavrilescu M Plants (Basel) 21-Mar-2024
PMCID:PMC10976221
doi:10.3390/plants13060913
PMID:38592933
Phenotypic Variations and Bioactive Constituents among Selected Ocimum Species Mulugeta SM, Pluhár Z, Radácsi P Plants (Basel) 24-Dec-2023
PMCID:PMC10780635
doi:10.3390/plants13010064
PMID:38202372
Pesticides vs. Biopesticides: From Pest Management to Toxicity and Impacts on the Environment and Human Health Daraban GM, Hlihor RM, Suteu D Toxics 04-Dec-2023
PMCID:PMC10748064
doi:10.3390/toxics11120983
PMID:38133384
Bioactive ZnO Nanoparticles: Biosynthesis, Characterization and Potential Antimicrobial Applications Huq MA, Apu MA, Ashrafudoulla M, Rahman MM, Parvez MA, Balusamy SR, Akter S, Rahman MS Pharmaceutics 16-Nov-2023
PMCID:PMC10675506
doi:10.3390/pharmaceutics15112634
PMID:38004613
An Overview of Cancer in Djibouti: Current Status, Therapeutic Approaches, and Promising Endeavors in Local Essential Oil Treatment Abdoul-Latif FM, Ainane A, Houmed Aboubaker I, Mohamed J, Ainane T Pharmaceuticals (Basel) 16-Nov-2023
PMCID:PMC10674319
doi:10.3390/ph16111617
PMID:38004482
The complete chloroplast genome of Ocimum basilicum L. var. basilicum (Lamiaceae) and its phylogenetic analysis Kirankumar SI, Balaji R, Tanuja, Parani M Mitochondrial DNA B Resour 30-Oct-2023
PMCID:PMC10769543
doi:10.1080/23802359.2023.2275835
PMID:38188439
Differential Antioxidant Response to Supplemental UV-B Irradiation and Sunlight in Three Basil Varieties Milić Komić S, Živanović B, Dumanović J, Kolarž P, Sedlarević Zorić A, Morina F, Vidović M, Veljović Jovanović S Int J Mol Sci 19-Oct-2023
PMCID:PMC10607338
doi:10.3390/ijms242015350
PMID:37895033
Enhanced Natural Strength: Lamiaceae Essential Oils and Nanotechnology in In Vitro and In Vivo Medical Research Kowalczyk T, Merecz-Sadowska A, Ghorbanpour M, Szemraj J, Piekarski J, Bijak M, Śliwiński T, Zajdel R, Sitarek P Int J Mol Sci 17-Oct-2023
PMCID:PMC10607815
doi:10.3390/ijms242015279
PMID:37894959
The complete chloroplast genome of Ocimum americanum Linnaeus 1755 and phylogenetic analysis among the Lamiaceae family Vineesh S, Balaji R, Tanuja, Parani M Mitochondrial DNA B Resour 16-Oct-2023
PMCID:PMC10583627
doi:10.1080/23802359.2023.2264545
PMID:37859799
Chemical Composition and Larvicidal Properties of Essential Oils from Wild and Cultivated Artemisia campestris L., an Endemic Plant in Morocco Alami A, El Ouali Lalami A, Annemer S, El-Akhal F, Ez zoubi Y, Farah A ScientificWorldJournal 09-Oct-2023
PMCID:PMC10578985
doi:10.1155/2023/5748133
PMID:37849964
Synergistic Repellent and Irritant Effects of a Mixture of β-Caryophyllene Oxide and Vetiver Oil against Mosquito Vectors Nararak J, Sanguanpong U, Sukkanon C, Manguin S, Chareonviriyaphap T Insects 20-Sep-2023
PMCID:PMC10532066
doi:10.3390/insects14090773
PMID:37754741
Green inspired synthesis of zinc oxide nanoparticles using Silybum marianum (milk thistle) extract and evaluation of their potential pesticidal and phytopathogens activities Jahan N, Rasheed K, Rahman KU, Hazafa A, Saleem A, Alamri S, Iqbal MO, Rahman MA PeerJ 14-Aug-2023
PMCID:PMC10434149
doi:10.7717/peerj.15743
PMID:37601248
Natural Products in Renal-Associated Drug Discovery Wruck W, Genfi AK, Adjaye J Antioxidants (Basel) 11-Aug-2023
PMCID:PMC10451693
doi:10.3390/antiox12081599
PMID:37627594
α-Terpineol Mitigates Dextran Sulfate Sodium-Induced Colitis in Rats by Attenuating Inflammation and Apoptosis Khan R, Jori C, Ansari MM, Ahmad A, Nadeem A, Siddiqui N, Sultana S ACS Omega 01-Aug-2023
PMCID:PMC10433518
doi:10.1021/acsomega.3c04317
PMID:37599911
Green synthesis of silver nanoparticles using Ocimum sanctum Linn. and its antibacterial activity against multidrug resistant Acinetobacter baumannii Gautam D, Dolma KG, Khandelwal B, Gupta M, Singh M, Mahboob T, Teotia A, Thota P, Bhattacharya J, Goyal R, M.R. Oliveira S, Pereira MD, Wiart C, Wilairatana P, Eawsakul K, Rahmatullah M, Saravanabhavan SS, Nissapatorn V PeerJ 28-Jul-2023
PMCID:PMC10389072
doi:10.7717/peerj.15590
PMID:37529215

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 / Phenol ethers / Anisoles
(E,E)-1,6-bis(4-methoxyphenyl)-1,5-hexadiene 11140953 Click to see COC1=CC=C(C=C1)C=CCCC=CC2=CC=C(C=C2)OC 294.40 unknown https://doi.org/10.1016/0031-9422(79)80152-1
1-Methoxy-4-[6-(4-methoxyphenyl)hexa-1,5-dienyl]benzene 85413178 Click to see COC1=CC=C(C=C1)C=CCCC=CC2=CC=C(C=C2)OC 294.40 unknown https://doi.org/10.1016/0031-9422(79)80152-1
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1002/FFJ.2730040104
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octen-3-OL 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1007/BF01959201
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown https://doi.org/10.1007/BF01959201
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1111/1750-3841.12457
https://doi.org/10.1007/BF01959201
https://doi.org/10.1016/0378-8741(89)90113-X
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1016/S0944-7113(11)80031-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1021/NP50018A028
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50018A028
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/NP50018A028
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
4,7,7-Trimethylbicyclo[4.1.0]hept-2-ene 530422 Click to see CC1CC2C(C2(C)C)C=C1 136.23 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1021/NP50018A028
Bergamotene 521569 Click to see CC(=CCCC1(C2CCC(=C)C1C2)C)C 204.35 unknown https://doi.org/10.1007/BF01959201
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1021/NP50018A028
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1016/S0944-7113(11)80031-0
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/NP50018A028
Camphor (synthetic) 159055 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1021/NP50018A028
Myrtenol 10582 Click to see CC1(C2CC=C(C1C2)CO)C 152.23 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
Sabinen 18818 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown https://doi.org/10.1021/NP50018A028
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1016/S0944-7113(11)80031-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1021/NP50018A028
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown https://doi.org/10.1021/NP50018A028
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/NP50018A028
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/NP50018A028
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,2S,3S,6R,7R,8R)-1,3-dimethyl-8-prop-1-en-2-yltricyclo[4.4.0.02,7]decan-3-ol 162901363 Click to see CC(=C)C1CCC2(C3C1C2C(CC3)(C)O)C 220.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
(1S,2S,3S,6R,7R,8Z)-8-(1-hydroxypropan-2-ylidene)-1,3-dimethyltricyclo[4.4.0.02,7]decan-3-ol 162893944 Click to see CC(=C1CCC2(C3C1C2C(CC3)(C)O)C)CO 236.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
11-Copaen-4-ol 14807653 Click to see CC(=C)C1CCC2(C3C1C2C(CC3)(C)O)C 220.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
2-[(1R,2R,3R,6S,7R)-6-methyl-8-methylidene-3-tricyclo[4.4.0.02,7]decanyl]propan-2-ol 162885927 Click to see CC12CCC(C3C1CCC(=C)C23)C(C)(C)O 220.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
4(15)-Copaen-11-ol 14807655 Click to see CC12CCC(C3C1CCC(=C)C23)C(C)(C)O 220.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
8-(1-Hydroxypropan-2-ylidene)-1,3-dimethyltricyclo[4.4.0.02,7]decan-3-ol 162893943 Click to see CC(=C1CCC2(C3C1C2C(CC3)(C)O)C)CO 236.35 unknown https://doi.org/10.1016/0031-9422(91)83755-A
beta-Cadinene 10657 Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C 204.35 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1007/BF01959201
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1021/NP50018A028
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1021/NP50018A028
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown https://doi.org/10.1021/NP50018A028
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
7-epi-alpha-Selinene 10123 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
alpha-Selinene 10856614 Click to see CC1=CCCC2(C1CC(CC2)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0944-7113(11)80031-0
https://doi.org/10.1021/NP50018A028
beta-Selinene 442393 Click to see CC(=C)C1CCC2(CCCC(=C)C2C1)C 204.35 unknown https://doi.org/10.1021/NP50018A028
https://doi.org/10.1016/S0944-7113(11)80031-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1007/BF02907824
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown https://doi.org/10.1016/J.FITOTE.2005.04.001
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Pilosin 12085264 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Isothymusin 630253 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)O)OC 330.29 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1016/S0031-9422(00)82238-4
Sorbifolin 3084390 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)O 300.26 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-o-Desmethylnobiletin 358832 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 388.40 unknown https://doi.org/10.1016/S0031-9422(00)00439-8
Nevadensin 160921 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/S0031-9422(00)82238-4
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown https://doi.org/10.1016/S0031-9422(00)00439-8

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.