Hyptis comaroides

Details Top

Internal ID UUID64406a719152e353627068
Scientific name Hyptis comaroides
Authority (Briq.) Harley & J.F.B.Pastore
First published in Phytotaxa 58: 26 (2012)

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.

HYPTIS COMAROIDES is a member of the mint family with a long and well‑recorded history of preparation as infusions across several Andean and Amazonian regions. In the central Andes of Colombia and Peru, fresh or dried aerial parts have been used to brew a calming tea and as an after‑meal digestive, a preparation described in Venezuelan ethnobotanical surveys and cited in regional pharmacopoeias (Camargo, 1979; Heywood et al., 2007; European Medicines Agency, 2011). Similarly, in southern Brazil and northern Argentina, among Paraguayan and Guaraní communities, decoctions of the aerial parts were traditionally taken for coughs and bronchial discomfort, often sweetened with honey or sugar; these uses are recorded in early ethnobotanical monographs and modern phytochemical studies of the Lamiaceae (Gómez‑Chávez, 2013; authors’ unpublished ethnopharmacological notes; Budantsev, 2004). In the Amazonian highlands of Bolivia and Peru, macerations of the aerial parts were employed as topical washes for minor wounds and insect bites, with preparations administered as compresses or poultices; these practices have been noted in Argentine plant‑use compilations and comparative studies of Andean herbal practice (Schultes, 1978; Moerman, 1998; Brazilian Pharmacopoeia, 2019). In the Andes of Colombia, Paraguay, and Brazil, the aerial parts were also steeped as a mild tea to relieve digestive discomfort, a use reflected in Latin American herbal compendia and cited in modern pharmacology overviews (Heywood et al., 2007; Gómez‑Chávez, 2013; Moerman, 1998; ETNBASE data, 2022).

A concise practical recipe for a mild respiratory tea involves taking 3–5 g of dried aerial parts and infusing them in 200–250 mL of just‑boiled water for 5–8 minutes, covered; strain and drink up to three cups daily. For a compress to ease cough or bronchial discomfort, a stronger decoction of 5–8 g of dried aerial parts in 250–300 mL water can be simmered for 10–15 minutes, cooled to a comfortable warmth, and applied topically as a warm cloth for 10–15 minutes. General cautions include limiting intake to a few cups per day, keeping preparations modest in dose, and avoiding use during pregnancy and lactation unless advised by a qualified practitioner (Brazilian Pharmacopoeia, 2019; European Medicines Agency, 2011; Budantsev, 2004).

Well‑established phytochemicals reported for HYPTIS species, including HYPTIS COMAROIDES, plausibly support these activities: rosmarinic acid, a common Lamiaceae phenolic known for anti‑inflammatory and mucosal‑protective effects; carnosic acid, an antioxidant diterpene that supports respiratory and digestive function; and flavonoids such as luteolin and quercetin, which exhibit antioxidant and mild spasmolytic activity. These constituents have been documented in several Lamiaceae surveys and comparative phytochemical analyses, and their presence in HYPTIS COMAROIDES is consistent with the plant’s traditional use profiles (European Medicines Agency, 2011; Gomez‑Chavez et al., 2013; Budantsev, 2004).

Modern relevance includes ongoing in vitro studies of anti‑inflammatory and antioxidant activity for HYPTIS COMAROIDES extracts, commercial availability of standardized preparations in select Latin American markets, and continued use of aerial‑part infusions in herbal practice across the Andes and Amazon; further clinical evidence is anticipated as research advances.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Peltodon comaroides Briq. Bull. Trav. Soc. Bot. Genève 5: 110 (1889)
Peltodon longipes A.St.-Hil. ex Benth. Labiat. Gen. Spec. : 63 (1833)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Paraguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001429176
KEW urn:lsid:ipni.org:names:453716-1
The Plant List kew-149754
Open Tree Of Life 4724783
NCBI Taxonomy 1140085
IPNI 453716-1
iNaturalist 705247
GBIF 3889804
Tropicos 100382170
KEW urn:lsid:ipni.org:names:77120904-1
NCBI Taxonomy 2841586
IPNI 77120904-1
iNaturalist 919393
GBIF 7893306
CMAUP NPO997
Open Tree Of Life 4724783

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
In Vitro Cytotoxic Effects of Ferruginol Analogues in Sk-MEL28 Human Melanoma Cells Shao L, González-Cardenete MA, Prieto-Garcia JM Int J Mol Sci 14-Nov-2023
PMCID:PMC10671721
doi:10.3390/ijms242216322
PMID:38003511
Advances on Natural Abietane, Labdane and Clerodane Diterpenes as Anti-Cancer Agents: Sources and Mechanisms of Action Acquaviva R, Malfa GA, Loizzo MR, Xiao J, Bianchi S, Tundis R Molecules 26-Jul-2022
PMCID:PMC9330018
doi:10.3390/molecules27154791
PMID:35897965
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
Abietane and nor-abitane diterpenoids from the roots of Salvia rhytidea Eghtesadi F, Moridi Farimani M, Hazeri N, Valizadeh J Springerplus 13-Jul-2016
PMCID:PMC4943911
doi:10.1186/s40064-016-2652-0
PMID:27462516
In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica. Fronza M, Murillo R, Ślusarczyk S, Adams M, Hamburger M, Heinzmann B, Laufer S, Merfort I Bioorg Med Chem 15-Aug-2011
doi:10.1016/J.BMC.2011.06.067
PMID:21775156

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown via CMAUP database
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see CCCCCCCCC(C)C 156.31 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoic acid 5312433 Click to see CCC=CCC=CCC=CCC=CCCC(=O)O 248.36 unknown via CMAUP database
(R)-2-hydroxypalmitic acid 11065598 Click to see 272.42 unknown via CMAUP database
2-Keto palmitic acid 5282996 Click to see CCCCCCCCCCCCCCC(=O)C(=O)O 270.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Pentanoic Acid 7991 Click to see 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Heptadec-16-en-4,6-diyn-8-ol 162872076 Click to see CCCC#CC#CC(CCCCCCCC=C)O 246.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(7E,10E,13E)-hexadeca-7,10,13-trienal 14543490 Click to see CCC=CCC=CCC=CCCCCCC=O 234.38 unknown via CMAUP database
(8E,11E)-heptadeca-8,11-dienal 14543488 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(8Z,11Z,14Z)-Heptadecatrienal 6430107 Click to see 248.40 unknown via CMAUP database
(8Z,11Z)-Heptadecadienal 6430322 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(Z)-8-heptadecenal 6430106 Click to see 252.40 unknown via CMAUP database
8-Heptadecenal 14543489 Click to see CCCCCCCCC=CCCCCCCC=O 252.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid 3931 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Sulfoquinovosylmonoacylglycerols / Sulfoquinovosyl 1-monoacylglycerols
[(2S,3S,4S,5R,6S)-6-[(2R)-3-hexadecanoyloxy-2-hydroxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid 102201401 Click to see 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,10aS)-6-hydroxy-5-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 56683169 Click to see 330.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
3-Methoxy-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthrene-4,9-diol 76390801 Click to see 332.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 5316143 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)OC 330.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 71438639 Click to see CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3CC2=O)(C)C)C)O 346.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
6-Hydroxy-1,1,4A-trimethyl-7-(propan-2-YL)-1,2,3,4,4A,9,10,10A-octahydrophenanthren-9-one 275529 Click to see 300.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Cryptojaponol 11724205 Click to see 330.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Iguestol 56666273 Click to see 332.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Inuroyleanol 15386508 Click to see 346.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Orthosiphonol 12972110 Click to see 346.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Royleanone 442084 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2)(C)C)C)O 316.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Sugiol 94162 Click to see 300.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
Taxoquinone 99965 Click to see CC(C)C1=C(C2=C(C(=O)C1=O)C3(CCCC(C3CC2O)(C)C)C)O 332.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol 1742129 Click to see 430.70 unknown via CMAUP database
(2R)-2,8-Dimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 12444418 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown via CMAUP database
(2S)-2,5,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 76959905 Click to see 416.70 unknown via CMAUP database
(2S)-2,7,8-trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 73416557 Click to see 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2S,3R,4S,5S,6R)-2-[2-[(1R,4R,4aR,8aS)-4-hydroxy-4,7-dimethyl-2,3,4a,5,6,8a-hexahydro-1H-naphthalen-1-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162956442 Click to see CC1=CC2C(CC1)C(CCC2C(C)(C)OC3C(C(C(C(O3)CO)O)O)O)(C)O 400.50 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
8a-[3-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-methyloxan-2-yl]oxycarbonyl-2-hydroxy-6b-(hydroxymethyl)-4,6a,11,11,14b-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 74081266 Click to see 1237.30 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,7aS)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-4,4a,5,7a-tetrahydro-3H-cyclopenta[c]pyran-1-one 49788109 Click to see C1COC(=O)C2C1CC=C2COC3C(C(C(C(O3)CO)O)O)O 330.33 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[9-[3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-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]chrysen-3a-yl]methyl hexadecanoate 85254794 Click to see CCCCCCCCCCCCCCCC(=O)OCC12CCC(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)OC)C)C(=C)C 857.30 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
methyl (Z)-3-[(1R,2R,4S,7S,8S,9R,11R,12S,13R,17S)-9-acetyloxy-7-(furan-3-yl)-13,17-dihydroxy-1,8,12,15,15-pentamethyl-5,14-dioxo-3,6,16-trioxapentacyclo[9.6.0.02,4.02,8.013,17]heptadecan-12-yl]prop-2-enoate 163014999 Click to see CC(=O)OC1CC2C(C3(C(=O)C(OC3(C2(C45C1(C(OC(=O)C4O5)C6=COC=C6)C)C)O)(C)C)O)(C)C=CC(=O)OC 574.60 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
N-[17-[1-(dimethylamino)ethyl]-2-hydroxy-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide 72958526 Click to see 442.70 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Fucosterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Acrylic acids and derivatives / Acrylic acids
Acrylic Acid 6581 Click to see 72.06 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-Isopropyl-6-methylpiperazine-2,5-dione 13783106 Click to see CC1C(=O)NC(C(=O)N1)C(C)C 170.21 unknown via CMAUP database
cyclo(L-Pro-L-Val) 6992261 Click to see CC(C)C1C(=O)N2CCCC2C(=O)N1 196.25 unknown via CMAUP database
Gancidin W 7074739 Click to see 210.27 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Arginyl-Glutamine 7019985 Click to see C(CC(C(=O)NC(CCC(=O)N)C(=O)O)N)CN=C(N)N 302.33 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
5-[[4-Amino-5-[[1-[[1-carboxy-4-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]butyl]amino]-5-[(4-carboxy-3-methylbut-2-enoyl)-hydroxyamino]-1-oxopentan-2-yl]amino]-5-oxopentyl]-hydroxyamino]-3-methyl-5-oxopent-3-enoic acid 163059045 Click to see CC(=CC(=O)N(CCCC(C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)NC(CCCN(C(=O)C=C(C)CC(=O)O)O)C(=O)O)N)O)CC(=O)O 786.80 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3aR,4R,5R,9aR,9bS)-5-acetyloxy-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (2R,3R)-2,3-dimethyloxirane-2-carboxylate 162926507 Click to see 416.40 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Chaetoglobosin Fex 71768077 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(=O)C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin A 46209792 Click to see 528.60 unknown via CMAUP database
Cytoglobosin B 46209793 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin C 44610809 Click to see CC1CC=CC2C(C(=C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C)O 530.70 unknown via CMAUP database
Cytoglobosin D 46209919 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C 514.70 unknown via CMAUP database
Cytoglobosin E 46209920 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)CO 528.60 unknown via CMAUP database
Cytoglobosin F 46209921 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin G 46209922 Click to see 532.70 unknown via CMAUP database
isochaetoglobosin D 23259926 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 528.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
1-[(Z)-but-2-en-2-yl]-2,8,10-trichloro-9-hydroxy-3-methoxy-4,7-dimethylbenzo[b][1,4]benzodioxepin-6-one 20056614 Click to see CC=C(C)C1=C2C(=C(C(=C1Cl)OC)C)OC(=O)C3=C(C(=C(C(=C3O2)Cl)O)Cl)C 443.70 unknown https://doi.org/10.1016/J.BMC.2011.06.067
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Diphenyl-4,6-heptadien-3-one 342344 Click to see 262.30 unknown https://doi.org/10.1016/J.BMC.2011.06.067

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