Cantinoa mutabilis

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Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

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

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Synonyms Top

Scientific name	Authority	First published in
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 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. coeruleum	Kuntze	Revis. Gen. Pl. 3(2): 260 (1898)
Mesosphaerum mutabile var. polystachyum	Kuntze	Revis. Gen. Pl. 2: 525 (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 spicata	Poit.	Ann. Mus. Hist. Nat. 7: 474 (1806)

Common names Top

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Language	Common/alternative name
ceb	hyptis mutabilis
Swedish	hyptis mutabilis
Vietnamese	hyptis mutabilis
war	hyptis mutabilis

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Southern Africa
  - Kwazulu-Natal

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- Southeastern U.S.A.
  - Alabama
  - Florida

Pacific click to expand
- Northwestern Pacific
  - Marianas

Southern America click to expand
- 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

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Database	ID/link to page
World Flora Online	wfo-0001333526
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

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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 / 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)-Tagetenone	6428432	Click to see CC(=CC(=O)C=C(C)C=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1995.9698469
Ipsdienone	6430826	Click to see CC(=CC(=O)CC(=C)C=C)C	150.22	unknown	https://doi.org/10.1080/10412905.1995.9698469
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	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 CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1021/NP50034A044
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50034A044 https://doi.org/10.1080/10412905.1995.9698469
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/10.1080/10412905.1995.9698469
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698469
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1021/NP50034A044 https://doi.org/10.1080/10412905.1995.9698469
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1021/NP50034A044 https://doi.org/10.1080/10412905.1995.9698469
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1995.9698469
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1080/10412905.1995.9698469
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/JPS.3080240410 https://doi.org/10.1021/NP50034A044
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1002/JPS.3080240410
trans-Borneol	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1995.9698469
> 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 CC1=CCC(CC1O)C(=C)C	152.23	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
Carvone, (+/-)-	7439	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 CC1=CC(=O)C(=C(C)C)CC1	150.22	unknown	https://doi.org/10.1080/10412905.1995.9698469
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1021/NP50034A044
(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 CC(=C1CCC(C(C1)(C)C(=C)C)(C)C=C)C	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
beta-Bisabolene	10104370	Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C	204.35	unknown	https://doi.org/10.1021/NP50034A044
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1080/10412905.1995.9698469
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 epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	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 CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	204.35	unknown	https://doi.org/10.1080/10412905.1995.9698469
delta-Elemene	12309449	Click to see CC(C)C1=CC(C(CC1)(C)C=C)C(=C)C	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 CC1=CCC(C=CCC(=CCC1)C)(C)C	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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	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
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/10.1021/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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC	470.70	unknown	https://doi.org/10.1021/NP50059A035
Methyl betulate	423298	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)OC	470.70	unknown	https://doi.org/10.1021/NP50059A035
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/10.1021/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
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/10.1021/NP50059A035

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Cantinoa mutabilis

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top