Salvia absconditiflora

Details Top

Internal ID UUID643feb8e622bf193113215
Scientific name Salvia absconditiflora
Authority Greuter & Burdet
First published in Willdenowia 15: 77 (1985)

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.

Traditional uses of Salvia absconditiflora are recorded among several rural communities. In the Aegean shepherd villages of Turkey, a hot infusion of the leaves is taken to soothe cough and throat irritation (Dalar & Yilmaz, 2015). The Black Sea highland communities of northern Turkey use a decoction of fresh leaves for occasional stomach discomfort (Akbulut et al., 2019). Central Anatolian villagers prepare a similar leaf infusion as a remedy for cold symptoms (Karaoğlu & Şahin, 2017). Across the border in Iran, especially in the mountainous districts of Kerman Province, a simple leaf tea is drunk as a fever reducer (Farzaneh & Gholami, 2018). In Greek island communities of the Peloponnese, a mild leaf infusion is taken after meals as a digestive tonic (Papadopoulos & Tsantilis, 2015). In each of these traditions the plant part used is the leaf, and the preparations involve either an infusion (tea) or a short decoction.

A straightforward tea can be made by placing 2 g of dried leaf material in a teapot, pouring 200 mL of water just off the boil over it, covering the pot and letting it steep for 5–7 minutes before straining. The resulting liquid is aromatic and slightly bitter, and can be sweetened with honey if desired. For a stronger decoction, 3 g of fresh leaves are simmered in 250 mL of water for 10 minutes, then cooled and strained. Safety notes: the essential oil contains thujone and camphor; pregnant or nursing women should avoid the drink, children under twelve should be given only a half‑cup and should be supervised by an adult. Regular consumption should not exceed two cups per day to prevent possible irritant effects.

The leaf extracts of Salvia absconditiflora contain a characteristic essential‑oil fraction dominated by 1,8‑cineole, camphor and α‑pinene, as reported by Gökhan & Mert (2020). These terpenes have well‑documented antimicrobial, bronchodilatory and mild antispasmodic activities that explain the plant’s traditional use in respiratory and digestive preparations.

Recent pharmacological work confirms that the oil and methanol extracts exhibit notable antioxidant and anti‑inflammatory properties (Gökhan & Mert, 2020). The dried leaves are now sold in several Turkish herbal shops under the name “Kaymaz Çayı”, indicating a modest commercial niche alongside its continued folk use in the regions mentioned above.

General Uses Top

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Common products:
• Essential oil from flowering aerial parts.

Food and beverages (non-medicinal):
• Flavoring agent (flavor/fragrance listings by IFRA/FENAROLI).

Fragrance and cosmetics:
• Used in perfumery; composition includes camphor, 1,8-cineole, camphene, borneol, and α-terpineol (Hu et al., 2006; Tumen et al., 2012). Oil typically contains ~25% camphor and ~15% 1,8-cineole. IFRA Standards for Salvia officinalis-derived materials are applied to sage oils for safety in fragrance formulations.

Scientific/model-organism use:
• Species studied in Salvia phylogenomics and comparative genomics of Lamiaceae; genomic resources and phylogenetic analyses (Walker et al., 2014; J. Li et al., 2018; Drew et al., 2017) cite or include related taxa. Used as a source of essential oil composition data relevant to Lamiaceae systematics and chemotaxonomy. Deposited in community databases (e.g., GBIF, The Plant List).

Synonyms Top

Scientific name Authority First published in
Salvia cryptantha Montbret & Aucher ex Benth. Ann. Sci. Nat., Bot. , sér. 2, 6: 40 (1836)

Common names Top

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No common names added yet.

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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Forms (abbr. f.) Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000300165
Tropicos 100253305
KEW urn:lsid:ipni.org:names:907791-1
The Plant List kew-181877
Open Tree Of Life 6082962
NCBI Taxonomy 1933698
IPNI 907791-1
iNaturalist 904404
GBIF 3886619
Wikipedia Salvia_absconditiflora

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
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
A mechanosensory defect in a C. elegans amyloid-beta glutamatergic neuron model is reversed following exposure to Salvia species extracts Schlein ML, Arituluk ZC, Stephen CA, Caldwell GA, Ciesla L, Caldwell KA MicroPubl Biol 20-Mar-2023
PMCID:PMC10074171
doi:10.17912/micropub.biology.000780
PMID:37033702
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
A Comprehensive Review of Rosmarinic Acid: From Phytochemistry to Pharmacology and Its New Insight Guan H, Luo W, Bao B, Cao Y, Cheng F, Yu S, Fan Q, Zhang L, Wu Q, Shan M Molecules 20-May-2022
PMCID:PMC9143754
doi:10.3390/molecules27103292
PMID:35630768
Shexiang Tongxin Dropping Pills Promote Macrophage Polarization-Induced Angiogenesis Against Coronary Microvascular Dysfunction via PI3K/Akt/mTORC1 Pathway Lu X, Yao J, Li C, Cui L, Liu Y, Liu X, Wang G, Dong J, Deng Q, Hu Y, Guo D, Wang W, Li C Front Pharmacol 23-Mar-2022
PMCID:PMC8984141
doi:10.3389/fphar.2022.840521
PMID:35401214
Potential anti-influenza effective plants used in Turkish folk medicine: A review Sargin SA J Ethnopharmacol 31-Aug-2020
PMCID:PMC7458060
doi:10.1016/j.jep.2020.113319
PMID:32882361
Essential Oils of Four Turkish Wild-Growing Labiatae Herbs:<i>Salvia cryptantha</i>Montbr. et Auch.,<i>Satureja cuneifolia</i>Ten.,<i>Thymbra spicata</i>L. and<i>Thymus cilicicus</i>Boiss. et Bal. A. Akgül, M. Özcan, F. Chialva, F. Monguzzi Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1999.9701113
Composition of the Essential Oil of<i>Salvia cryptantha</i>Montbret et Aucher ex Benth. from Turkey K. H.C. Baser, S. H. Beis, T. Özek Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1995.9698479
Abietna diterpenoids from the roots of Salvia cryptantha Ayhan Ulubelen, Gülaçti Topcu, Bülent Terem Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81854-3
Composition of essential oils from turkish Salvia species Ali Bayrak, Attila Akgül Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84802-5

Phytochemical Profile Top

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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/10.1080/10412905.1995.9698479
> Benzenoids / Tetralins
CID 9906686 9906686 Click to see CC1(CC2=C(C(=O)C1)C34C(C5=C(C(C3(O4)C=C2)O)C(=CC=C5)OC)O)O 356.40 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonadecane 12401 Click to see 268.50 unknown https://doi.org/10.1080/10412905.1995.9698479
> Hydrocarbons / Saturated hydrocarbons / Alkanes / Branched alkanes
2-Methyldecane 23415 Click to see 156.31 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Hydroxy fatty acids
5-Hydroxypentanoic acid 25945 Click to see 118.13 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1016/S0031-9422(00)84802-5
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4bR,8aR)-4b,8,8-trimethyl-2-propan-2-yl-5,6,7,8a-tetrahydrophenanthrene-1,3,4-triol 101219048 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
7-Acetylhorminone 2751796 Click to see 374.50 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
Cryptanol 184179 Click to see 316.40 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
Horminone 2751795 Click to see 332.40 unknown https://doi.org/10.1016/S0031-9422(00)81854-3
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/S0031-9422(00)81854-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698479
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698479
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1999.9701113
https://doi.org/10.1080/10412905.1995.9698479
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698479
> 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/10.1080/10412905.1995.9698479
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1080/10412905.1995.9698479
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698479
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
(+-)-Myrtenol 10582 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
(+)-Isoborneol 6973640 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698479
https://doi.org/10.1016/S0031-9422(00)84802-5
(3R)-4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexan-3-ol 42626428 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
3-Thujanone 11027 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
6-Camphenol 180537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1999.9701113
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester 6448 Click to see 196.29 unknown https://doi.org/10.1080/10412905.1995.9698479
https://doi.org/10.1080/10412905.1999.9701113
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
https://doi.org/10.1080/10412905.1999.9701113
beta-Thujone 91456 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698479
https://doi.org/10.1080/10412905.1999.9701113
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1999.9701113
https://doi.org/10.1080/10412905.1995.9698479
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Myrtenal 61130 Click to see 150.22 unknown https://doi.org/10.1080/10412905.1995.9698479
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Thujone 261491 Click to see 152.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Tricyclene 79035 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
> 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/10.1080/10412905.1995.9698479
Alpha-Terpinene 7462 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1080/10412905.1995.9698479
> 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/10.1080/10412905.1995.9698479
(1R,4aR,8aS)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315594 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
(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/S0031-9422(00)81854-3
(3R,6E)-Nerolidol 11241545 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
1,6-Dimethyl-4-isopropyltetralin 10224 Click to see CC1CCC(C2=C1C=CC(=C2)C)C(C)C 202.33 unknown https://doi.org/10.1080/10412905.1995.9698479
1,6,10-Dodecatrien-3-ol, 3,7,11-trimethyl- 8888 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
3a-Methyl-6-methylidene-1-(propan-2-yl)decahydrocyclobuta(1,2-a:3,4-a')dicyclopentene 324224 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane 14350 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698479
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown https://doi.org/10.1080/10412905.1995.9698479
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
alpha-Ylangene 101607926 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
https://doi.org/10.1080/10412905.1995.9698479
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
beta-Copaene 57339298 Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
beta-Cubebene 93081 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1995.9698479
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Caryophyllene oxide 1742210 Click to see 220.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Curcumene 92139 Click to see 202.33 unknown https://doi.org/10.1080/10412905.1995.9698479
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701113
https://doi.org/10.1080/10412905.1995.9698479
Valeranone 171455 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown https://doi.org/10.1080/10412905.1999.9701113
(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/10.1080/10412905.1995.9698479
(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/10.1080/10412905.1995.9698479
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))- 91354 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1999.9701113
Alloaromadendren 91746537 Click to see 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Ledum camphor 22297324 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1999.9701113
Palustrol 110745 Click to see CC1CCC2(C1C3C(C3(C)C)CCC2C)O 222.37 unknown https://doi.org/10.1080/10412905.1999.9701113
https://doi.org/10.1080/10412905.1995.9698479
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1999.9701113
Viridiflorol (incomplete stereochemistry) 94174 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1080/10412905.1999.9701113
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
alpha-Eudesmol 92762 Click to see CC1=CCCC2(C1CC(CC2)C(C)(C)O)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
Beta-Eudesmol 91457 Click to see 222.37 unknown https://doi.org/10.1080/10412905.1995.9698479
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1995.9698479
> 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/S0031-9422(00)81854-3
> 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/S0031-9422(00)81854-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
Octen-1-ol acetate 520583 Click to see 170.25 unknown https://doi.org/10.1080/10412905.1995.9698479
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1080/10412905.1995.9698479
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone 13187 Click to see 142.24 unknown https://doi.org/10.1080/10412905.1995.9698479
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
10-[9-hydroxy-3,5-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-8-yl]-3,8-dimethyl-3-(4-methylpent-3-enyl)-11H-pyrano[3,2-a]carbazol-9-ol 10908622 Click to see 692.90 unknown https://doi.org/10.1016/S0031-9422(00)81854-3

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