Lepechinia caulescens - Unknown
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Internal ID UUID643fe10fa4571645720076
Scientific name Lepechinia caulescens
Authority (Ortega) Epling
First published in Repert. Spec. Nov. Regni Veg. Beih. 85: 20 (1935)

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Synonyms Top

Scientific name Authority First published in
Horminum caulescens Ortega Nov. Rar. Pl. Descr. Dec. : 63 (1798)
Lepechinia spicata Willd. Hort. Berol. 1: 21 (1804)
Ulricia pyramidata Jacq. ex Steud. Nomencl. Bot. 1: 862 (1821)

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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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000226021
Tropicos 17603310
KEW urn:lsid:ipni.org:names:137865-2
The Plant List kew-110763
Open Tree Of Life 905466
NCBI Taxonomy 980664
IPNI 137865-2
iNaturalist 286956
GBIF 3888938
CMAUP NPO8086

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
Hairy Root Cultures as a Source of Phenolic Antioxidants: Simple Phenolics, Phenolic Acids, Phenylethanoids, and Hydroxycinnamates Malarz J, Yudina YV, Stojakowska A Int J Mol Sci 07-Apr-2023
PMCID:PMC10138958
doi:10.3390/ijms24086920
PMID:37108084
Biotic Elicitors in Adventitious and Hairy Root Cultures: A Review from 2010 to 2022 Alcalde MA, Perez-Matas E, Escrich A, Cusido RM, Palazon J, Bonfill M Molecules 17-Aug-2022
PMCID:PMC9416168
doi:10.3390/molecules27165253
PMID:36014492
Bioassay-Guided extraction of andrographis paniculata for intervention of in-vitro prostate cancer progression in metabolic syndrome environment Idris MK, Hasham R, Ismail HF Daru 03-Aug-2022
PMCID:PMC9715910
doi:10.1007/s40199-021-00414-8
PMID:35922691
Exploration of Lamiaceae in Cardio Vascular Diseases and Functional Foods: Medicine as Food and Food as Medicine Chakrabartty I, Mohanta YK, Nongbet A, Mohanta TK, Mahanta S, Das N, Saravanan M, Sharma N Front Pharmacol 14-Jun-2022
PMCID:PMC9237463
doi:10.3389/fphar.2022.894814
PMID:35774598
Contributions from Mexican Flora for the Treatment of Diabetes Mellitus: Molecules of Psacalium decompositum (A. Gray) H. Rob & Brettell Jiménez-Estrada M, Huerta-Reyes M, Tavera-Hernández R, Alvarado-Sansininea JJ, Alvarez AB Molecules 13-May-2021
PMCID:PMC8153299
doi:10.3390/molecules26102892
PMID:34068304
Methyl jasmonate enhances ursolic, oleanolic and rosmarinic acid production and sucrose induced biomass accumulation, in hairy roots of Lepechinia caulescens Vergara-Martínez VM, Estrada-Soto SE, Valencia-Díaz S, Garcia-Sosa K, Peña-Rodríguez LM, Arellano-García JD, Perea-Arango I PeerJ 27-Apr-2021
PMCID:PMC8086586
doi:10.7717/peerj.11279
PMID:33986996
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Plants Used as Antihypertensive Verma T, Sinha M, Bansal N, Yadav SR, Shah K, Chauhan NS Nat Prod Bioprospect 11-Nov-2020
PMCID:PMC7981375
doi:10.1007/s13659-020-00281-x
PMID:33174095
Antihypertensive activity and vascular reactivity mechanisms of Vitex pubescens leaf extracts in spontaneously hypertensive rats Al-Akwaa AA, Asmawi MZ, Dewa A, Mahmud R Heliyon 31-Jul-2020
PMCID:PMC7399130
doi:10.1016/j.heliyon.2020.e04588
PMID:32775735
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

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 / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Meridinol 11079164 Click to see C1C(C(C(=O)O1)(CC2=CC3=C(C=C2)OCO3)O)CC4=CC5=C(C=C4)OCO5 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aR,4bS,7S,10aR)-7-ethyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 59733709 Click to see CCC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C 304.50 unknown via CMAUP database
(1R,4aS,10aR)-7-Isopropyl-1,4a-dimethyl-1,2,3,4,4a,9,10,10a-octahydrophenanthrene-1-carboxylic acid 10017708 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
15-norlabda-8(20),12E-diene-14-carboxaldehyde-19-oic acid 44592589 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=O 304.40 unknown via CMAUP database
Communic Acid 637125 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dehydroabietinol 15586718 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)CO)C 286.50 unknown via CMAUP database
Dihydrosandaracopimaric acid 21139472 Click to see CCC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 304.50 unknown via CMAUP database
Methyl 15-hydroxydehydroabietate 11573479 Click to see CC12CCCC(C1CCC3=C2C=CC(=C3)C(C)(C)O)(C)C(=O)OC 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
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/J.FITOTE.2004.10.007
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1016/J.FITOTE.2004.10.007
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1016/J.FITOTE.2004.10.007
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epijuvabione 10923485 Click to see CC(C)CC(=O)CC(C)C1CCC(=CC1)C(=O)OC 266.38 unknown via CMAUP database
(+)-Nerolidol 5356544 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
4-[(E)-1,5-Dimethyl-3-oxo-1-hexenyl]benzoic acid methyl ester 15834297 Click to see CC(C)CC(=O)C=C(C)C1=CC=C(C=C1)C(=O)OC 260.33 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Atlantolone 101949827 Click to see CC1=CCC(CC1)C(=CC(=O)CC(C)(C)O)C 236.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/J.FITOTE.2004.10.007
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/J.FITOTE.2004.10.007
Epijuvabiol 14396628 Click to see CC(C)CC(CC(C)C1CCC(=CC1)C(=O)OC)O 268.39 unknown via CMAUP database
Methyl atlantonate 14192388 Click to see CC(C)CC(=O)C=C(C)C1CCC(=CC1)C(=O)OC 264.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,1abeta,1balpha,6abeta)-1beta-Isopropyl-2-methylene-5abeta-methyldecahydrocyclopropa[a]indene-5beta-ol 101949829 Click to see CC(C)C1C2C1C3C(=C)CCC(C3(C2)C)O 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/J.LFS.2006.03.006
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1016/0031-9422(92)83466-C
https://doi.org/10.1016/S0031-9422(00)89540-0
Euscaphic acid 471426 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(92)83466-C
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
https://doi.org/10.1016/0031-9422(92)83466-C
Methyl oleanolate 92900 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)OC)C 470.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)83466-C
https://doi.org/10.1016/S0031-9422(00)89540-0
https://doi.org/10.1016/J.LFS.2006.03.006
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1016/0031-9422(92)83466-C
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
https://doi.org/10.1016/0031-9422(92)83466-C
Ursolic acid methyl ester 89432794 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
beta-Sitosterone 9801811 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(=O)C4)C)C)C(C)C 412.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)89540-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-4',5,7-Trihydroxy-6-methylflavanone 59072631 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)- 667544 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5-Hydroxy-6-methyl-7-methoxyflavanone 14583633 Click to see CC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC 284.31 unknown via CMAUP database
(S)-5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-methylchroman-4-one 15834295 Click to see CC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)OC 300.30 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/0031-9422(92)83466-C
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/10.1016/0031-9422(92)83466-C
> Phenylpropanoids and polyketides / Stilbenes
1,2-Bis(4-hydroxy-3-methoxyphenyl)ethylene 5280698 Click to see COC1=C(C=CC(=C1)C=CC2=CC(=C(C=C2)O)OC)O 272.29 unknown via CMAUP database

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