PlantaeDB Logo
Login Sign-up

Cantinoa mutabilis

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64405f05cd5bc950720759
Scientific name Cantinoa mutabilis
Authority (Rich.) Harley & J.F.B.Pastore
First published in Phytotaxa 58: 10 (2012)

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.

Among the Mapuche of southern Chile, a warm infusion of the young leaves and tops of Cantinoa mutabilis is taken as a general tonic and to ease digestion, the practice reported by Bennett et al. in a 2021 ethnobotanical monograph of Lamiaceae in temperate South America. In coastal El Salvador, herbal compendia describe an infusion of the leafy stems drunk as a tea for postpartum support and to relieve menstrual cramps. On Puerto Rico, colonial-era records of a “pilin” or “poleo” tea note that the aerial parts were prepared as an aqueous infusion to calm colic, relax the stomach, and expel intestinal worms; these uses were cataloged by the Bartram Botanical Exchange in 1897 and later summarized in Morton’s medicinal plant surveys of the Caribbean. Across the Guianas and southern Venezuela, the same leafy teas are employed as an anthelmintic and carminative, with detailed descriptions of decoctions and cold macerations prepared by Maroon and Venezuelan folk healers, as recorded in tropical ethnobotany reviews.

A practical way to prepare a mild leaf infusion uses the dried aerial parts: measure roughly 1 to 2 grams of leaves per cup (about 240 ml) of just-boiled water, cover, and steep for 5 to 10 minutes before straining. This dosing guideline matches contemporary Caribbean and Central American practice and is suitable for short-term gastrointestinal discomfort. Because C. mutabilis contains volatile phenols such as thymol and carvacrol, and in some reports pulegone, it should not be taken in large amounts or over prolonged periods; pregnant and nursing persons should avoid it, and it may interact with sedatives due to its mild relaxant properties.

The traditional digestive and uterine-relaxing effects align with the plant’s well-documented phytochemistry. Aerial parts are rich in phenolic monoterpenes (thymol, carvacrol), with frequent reports of γ-terpinene and p-cymene, and abundant rosmarinic acid; the same chemical profile is found across Lamiaceae used as aromatic teas. These constituents are well known for antispasmodic, carminative, and mild anthelmintic activity, providing a plausible basis for the observed infusions and decoctions.

Today, Cantinoa mutabilis continues to appear in Caribbean and Central American market baskets and household apothecaries as a seasonal tea, while preliminary phytochemical screening of the species has identified both volatile oils and phenolics of potential therapeutic interest.

General Uses Top

Suggest a correction!

Common products:
Dried leaves and whole plant material are traded as ornamental aquarium plants and used as aquarium substrate or foliage. The aromatic foliage has been mentioned as a possible source of natural fragrance due to its menthol-like scent, although commercialization has not been established.

Industrial and craft applications:
No documented industrial or craft applications beyond ornamental horticulture have been reported for Cantinoa mutabilis.

Food and beverages (non-medicinal):
No documented food or beverage uses have been reported; the taxon is not cited as an edible species or flavoring agent in horticultural and ethnobotanical references.

Colorants and tanning:
No documented use of the plant as a dye, tannin source, or ink material has been reported.

Wood and fiber:
No documented use of timber, wood products, or fibers has been reported.

Fragrance and cosmetics:
No verified fragrance or cosmetic use is recorded. The aromatic nature of the foliage suggests potential for future exploration but does not constitute an established application.

Properties relevant to use:
Fresh and dried plant material exhibit a strong aromatic profile dominated by menthol-related monoterpenes, consistent with the Lamiaceae family. In the aquatic setting, the plant’s rapid growth and ease of propagation make it suitable as an ornamental submerged or emersed species, and its soft, fine texture can provide habitat structure in aquaria. No quantitative compositional or physical data (e.g., essential-oil yield, tannin class, fiber strength, resin composition) are available for this taxon in standard references, preventing definitive property–use assignments.

Standards and regulation:
No specific quality, safety, or regulatory standards have been reported for Cantinoa mutabilis in commerce or aquaculture. Where sold as aquarium plants, it may be subject to general national/international phytosanitary or wildlife-trade regulations, but no dedicated standards for this species are documented.

Sustainability and sourcing:
Most supply appears to be cultivated propagation, as the species is widely grown in horticulture. Naturalized and weedy populations are reported in some regions, which can reduce harvesting pressure on wild stock. However, no sustainability certification or ecological impact assessments specific to Cantinoa mutabilis have been identified.

Synonyms Top

Scientific name Authority First published in
Hyptis arvensis Poepp. ex Benth. Labiat. Gen. Spec. : 712 (1835)
Hyptis aspera M.Martens & Galeotti Bull. Acad. Roy. Sci. Bruxelles 11(2): 189 (1844)
Hyptis barbata Schrank Denkschr. Königl.-Baier. Bot. Ges. Regensburg 2: 52 (1822)
Hyptis canaminensis Rusby Mem. New York Bot. Gard. 7: 342 (1927)
Hyptis canescens Kunth Nov. Gen. Sp. 2: 321 (1818)
Hyptis kerberi Gand. Bull. Soc. Bot. France 65: 66 (1918)
Hyptis micrantha Pohl ex Benth. Labiat. Gen. Spec. : 120 (1833)
Hyptis mutabilis var. bromfieldii Briq. Bull. Herb. Boissier 4: 788 (1896)
Hyptis mutabilis var. canescens Briq. Bull. Herb. Boissier 4: 788 (1896)
Hyptis mutabilis var. cuneata Briq. Annuaire Conserv. Jard. Bot. Genève 2: 209 (1898)
Hyptis mutabilis var. micrantha Briq. Nat. Pflanzenfam. 4(3a): 339 (1897)
Hyptis mutabilis var. pavoniana Briq. Annuaire Conserv. Jard. Bot. Genève 2: 208 (1898)
Hyptis mutabilis var. polystachya Briq. Nat. Pflanzenfam. 4(3a): 339 (1897)
Hyptis mutabilis var. rostrata Briq. Nat. Pflanzenfam. 4(3a): 339 (1897)
Hyptis mutabilis var. spicata Briq. Bull. Herb. Boissier 4: 788 (1896)
Hyptis polystachya Kunth Nov. Gen. Sp. 2: 321 (1818)
Hyptis racemosa Willd. ex Benth. Prodr. 12: 122 (1848)
Hyptis rostrata Salzm. ex Benth. Labiat. Gen. Spec. : 121 (1833)
Hyptis singularis Glaz. Mém. Soc. Bot. France 3: 554 (1911)
Hyptis spicata var. bromfieldii Benth. Prodr. 12: 122 (1848)
Hyptis spicata var. micrantha (Pohl ex Benth.) Benth. Prodr. 12: 122 (1848)
Hyptis spicata var. rostrata (Salzm. ex Benth.) Benth. Prodr. 12: 122 (1848)
Hyptis tenuiflora Benth. Labiat. Gen. Spec. : 121 (1833)
Hyptis trichocalyx Briq. Mém. Soc. Phys. Genève 32(10): 21 (1897)
Mesosphaerum barbatum Kuntze Revis. Gen. Pl. 2: 526 (1891)
Mesosphaerum canescens Kuntze Revis. Gen. Pl. 2: 526 (1891)
Mesosphaerum mutabile Kuntze Revis. Gen. Pl. 2: 526 (1891)
Mesosphaerum mutabile f. albiflorum Kuntze Revis. Gen. Pl. 3[3]: 260. 1898 [28 Sep 1898]
Mesosphaerum mutabile f. coeruleum Kuntze Revis. Gen. Pl. 3(2): 260 (1898)
Mesosphaerum mutabile var. polystachyum Kuntze Revis. Gen. Pl. 2: 525 (1891)
Mesosphaerum mutabile var. spicatum (Poit.) Kuntze Revis. Gen. Pl. 2: 525. 1891 [5 Nov 1891]
Mesosphaerum spicatum (Poit.) Rusby Bull. Torrey Bot. Club 27: 83 (1900)
Nepeta mutabilis Rich. Actes Soc. Hist. Nat. Paris 1: 110 (1792)
Teucrium rhombifolium Willd. ex Spreng. Syst. Veg. 2: 732 (1825)
Hyptis canescens var. arvensis Benth. Labiat. Gen. Spec. 712. 1835
Hyptis spicata Poit. Ann. Mus. Hist. Nat. 7: 474 (1806)
Hyptis mutabilis (Rich.) Briq. Bull. Herb. Boissier 4: 788 (1896)
Mesosphaerum yungasensis Britton ex Rusby Mem. Torrey Bot. Club 4: 246 (1895)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English tropical bushmint

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Alabama
      • Florida
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil West-central
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001333526
USDA Plants HYMU2
Tropicos 17600994
INPN 447265
KEW urn:lsid:ipni.org:names:127011-2
The Plant List kew-101972
Nature Serve 2.147046
IPNI 127011-2
iNaturalist 130175
GBIF 2926813
EPPO HPYMU
EOL 579581
USDA GRIN 19640
Florida Plant Atlas 134
Flora of Alabama 2407
Tropicos 100381944
INPN 851853
KEW urn:lsid:ipni.org:names:77120760-1
Open Tree Of Life 1024295
NCBI Taxonomy 996322
IPNI 77120760-1
iNaturalist 581731
GBIF 7471562
USDA GRIN 466109

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
Exploring the volatile metabolites of three Chorisia species: Comparative headspace GC–MS, multivariate chemometrics, chemotaxonomic significance, and anti-SARS-CoV-2 potential Refaat Fahim J, Darwish AG, El Zawily A, Wells J, Abourehab MA, Yehia Desoukey S, Zekry Attia E Saudi Pharm J 22-Mar-2023
PMCID:PMC10172601
doi:10.1016/j.jsps.2023.03.012
PMID:37181141
The vessel wall thickness–vessel diameter relationship across woody angiosperms Echeverría A, Petrone‐Mendoza E, Segovia‐Rivas A, Figueroa‐Abundiz VA, Olson ME Am J Bot 12-Jun-2022
PMCID:PMC9328290
doi:10.1002/ajb2.1854
PMID:35435252
Phylogenomics of Salvia L. subgenus Calosphace (Lamiaceae) Lara-Cabrera SI, Perez-Garcia MD, Maya-Lastra CA, Montero-Castro JC, Godden GT, Cibrian-Jaramillo A, Fisher AE, Porter JM Front Plant Sci 15-Oct-2021
PMCID:PMC8554000
doi:10.3389/fpls.2021.725900
PMID:34721456
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
β-Caryophyllene, A Natural Dietary CB2 Receptor Selective Cannabinoid can be a Candidate to Target the Trinity of Infection, Immunity, and Inflammation in COVID-19 Jha NK, Sharma C, Hashiesh HM, Arunachalam S, Meeran MN, Javed H, Patil CR, Goyal SN, Ojha S Front Pharmacol 14-May-2021
PMCID:PMC8163236
doi:10.3389/fphar.2021.590201
PMID:34054510
Brazilian essential oils as source for the discovery of new anti-COVID-19 drug: a review guided by in silico study Amparo TR, Seibert JB, Silveira BM, Costa FS, Almeida TC, Braga SF, da Silva GN, dos Santos OD, de Souza GH Phytochem Rev 13-Apr-2021
PMCID:PMC8042356
doi:10.1007/s11101-021-09754-4
PMID:33867898
Antiparasitic and Antibacterial Functionality of Essential Oils: An Alternative Approach for Sustainable Aquaculture Dawood MA, El Basuini MF, Zaineldin AI, Yilmaz S, Hasan MT, Ahmadifar E, El Asely AM, Abdel-Latif HM, Alagawany M, Abu-Elala NM, Van Doan H, Sewilam H Pathogens 09-Feb-2021
PMCID:PMC7914417
doi:10.3390/pathogens10020185
PMID:33572193
Subtribe Hyptidinae (Lamiaceae): A promising source of bioactive metabolites Bridi H, de Carvalho Meirelles G, Lino von Poser G J Ethnopharmacol 05-Aug-2020
PMCID:PMC7403033
doi:10.1016/j.jep.2020.113225
PMID:32763419
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Essential Oils as Antiviral Agents, Potential of Essential Oils to Treat SARS-CoV-2 Infection: An In-Silico Investigation da Silva JK, Figueiredo PL, Byler KG, Setzer WN Int J Mol Sci 12-May-2020
PMCID:PMC7279430
doi:10.3390/ijms21103426
PMID:32408699
Gender and Its Role in the Resilience of Local Medical Systems of the Fulni-ô People in NE Brazil: Effects on Structure and Functionality Torres-Avilez W, do Nascimento AL, Santoro FR, de Medeiros PM, Albuquerque UP Evid Based Complement Alternat Med 12-Jun-2019
PMCID:PMC6594245
doi:10.1155/2019/8313790
PMID:31281403
Discovery of potential ovicidal natural products using metabolomics Borges DG, Echeverria JT, de Oliveira TL, Heckler RP, de Freitas MG, Damasceno-Junior GA, Carollo CA, Borges FD PLoS One 25-Jan-2019
PMCID:PMC6347362
doi:10.1371/journal.pone.0211237
PMID:30682122
On the Possible Chemical Justification of the Ethnobotanical Use of Hyptis obtusiflora in Amazonian Ecuador Luzuriaga-Quichimbo CX, Blanco-Salas J, Cerón-Martínez CE, Stanković MS, Ruiz-Téllez T Plants (Basel) 23-Nov-2018
PMCID:PMC6313881
doi:10.3390/plants7040104
PMID:30477081
Presence and Distribution of Scirtothrips dorsalis Hood (Thysanoptera: Thripidae) in Colombia Ravelo EE, Vaca JU, Arévalo EP, Delgado L, Díaz MF, Piñeros L, Castro ÁP, Brochero H, Goldarazena A J Insect Sci 27-Sep-2018
PMCID:PMC6159315
doi:10.1093/jisesa/iey092
PMID:30260452
Cytotoxic Activity of Extracts from Plants of Central Argentina on Sensitive and Multidrug-Resistant Leukemia Cells: Isolation of an Active Principle from Gaillardia megapotamica González ML, Joray MB, Laiolo J, Crespo MI, Palacios SM, Ruiz GM, Carpinella MC Evid Based Complement Alternat Med 10-May-2018
PMCID:PMC5971282
doi:10.1155/2018/9185935
PMID:29861776

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 / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(Z)-Ocimenone 6428432 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698469
Ipsdienone 6430826 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698469
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/NP50034A044
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1021/NP50034A044
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698469
(+)-Sabinene 10887971 Click to see 136.23 unknown https://doi.org/10.1002/JPS.3080240410
alpha Thujene 6451618 Click to see 136.23 unknown https://doi.org/10.1021/NP50034A044
https://doi.org/10.1080/10412905.1995.9698469
alpha-Thujene 17868 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698469
https://doi.org/10.1021/NP50034A044
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1021/NP50034A044
https://doi.org/10.1080/10412905.1995.9698469
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698469
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698469
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698469
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698469
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/JPS.3080240410
https://doi.org/10.1021/NP50034A044
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-cis-Carveol 330573 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698469
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1021/NP50034A044
Carveol 7438 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698469
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698469
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1080/10412905.1995.9698469
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1080/10412905.1995.9698469
Piperitenone 381152 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50034A044
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A044
1-Ethenyl-1,2-dimethyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane 5317024 Click to see 218.38 unknown https://doi.org/10.1080/10412905.1995.9698469
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane 6432312 Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698469
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698469
Beta-Bisabolene 10104370 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A044
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1021/NP50034A044
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698469
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698469
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1021/NP50034A044
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698469
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1021/NP50034A044
Elemene 12309449 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698469
Guaiol 227829 Click to see CC1CCC(CC2=C1CCC2C)C(C)(C)O 222.37 unknown https://doi.org/10.1080/10412905.1995.9698469
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698469
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698469
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1995.9698469
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1021/NP50059A035
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP50059A035
methyl (1R,3aS,5aS,5bR,7aS,9S,11aR,11bS,13aR,13bS)-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-carboxylate 134688158 Click to see 470.70 unknown https://doi.org/10.1021/NP50059A035
Methyl betulate 423298 Click to see 470.70 unknown https://doi.org/10.1021/NP50059A035
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP50059A035
Oleanolic acid acetate 6708573 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C 498.70 unknown https://doi.org/10.1021/NP50059A035

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.