Scientific name	Authority	First published in
Laurus teneriffae	Poir.	Encycl. , Suppl. 3: 322 (1813)
Laurus indica	L.	Sp. Pl. : 370 (1753)
Ocotea indica	(L.) Kostel.	Allg. Med.-Pharm. Fl. 2: 482 (1833)
Phoebe indica	(L.) Pax	Nat. Pflanzenfam. 3(2): 115 (1889)
Persea pseudoindica	Link	Handbuch 1: 389 (1829)
Persea teneriffae	F.Muell.	Select Pl. , ed. 2: 159 (1876)
Borbonia indica	(L.) J.Presl	Prir. Rostlin 2: 57 (1825)
Laurus americana	Nees	Syst. Laur.: 135 (1836)

Common names Top

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Filter by language:

Language	Common/alternative name
Spanish	viñatigo
Arabic	برساء هندية
Bulgarian	индийска персея
Czech	hruškovec indický
German	indische persea
Esperanto	makaronezia perseo
Finnish	makaronesianavokado
Russian	Персея индийская
Chinese	印度鳄梨

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

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000465062
Tropicos	17801323
INPN	968737
Flora of Italy	8565
KEW	urn:lsid:ipni.org:names:468067-1
The Plant List	kew-2529655
Open Tree Of Life	9684
Observations.org	129127
NCBI Taxonomy	136127
IUCN Red List	30329
IPNI	468067-1
iNaturalist	336802
GBIF	4181596
Freebase	/m/02xc4yv
EPPO	PEBIN
EOL	5394782
USDA GRIN	27402
Wikipedia	Persea_indica
CMAUP	NPO21875

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

Differential Volatile Organic Compound Expression in the Interaction of Daldinia eschscholtzii and Mycena citricolor

Escudero-Leyva E, Quirós-Guerrero L, Vásquez-Chaves V, Pereira-Reyes R, Chaverri P, Tamayo-Castillo G

ACS Omega

18-Aug-2023

PMCID:	PMC10468842
doi:	10.1021/acsomega.3c03865
PMID:	37663497

Chemical characteristics of the sesquiterpenes and diterpenes from Lauraceae family and their multifaceted health benefits: A review

Feng H, Jiang Y, Cao H, Shu Y, Yang X, Zhu D, Shao M

Heliyon

07-Dec-2022

PMCID:	PMC9801090
doi:	10.1016/j.heliyon.2022.e12013
PMID:	36590503

Antidiabetic Potential of Plants from the Caribbean Basin

Méril-Mamert V, Ponce-Mora A, Sylvestre M, Lawrence G, Bejarano E, Cebrián-Torrejón G

Plants (Basel)

20-May-2022

PMCID:	PMC9146409
doi:	10.3390/plants11101360
PMID:	35631785

Samarium(ii) iodide-mediated reactions applied to natural product total synthesis

Heravi MM, Nazari A

RSC Adv

30-Mar-2022

PMCID:	PMC8965710
doi:	10.1039/d1ra08163b
PMID:	35424959

Extraction and determination of flubendiamide insecticide in food samples: A review

Aghris S, Alaoui OT, Laghrib F, Farahi A, Bakasse M, Saqrane S, Lahrich S, El Mhammedi MA

Curr Res Food Sci

14-Feb-2022

PMCID:	PMC8861570
doi:	10.1016/j.crfs.2022.02.005
PMID:	35243353

Sustainable Production of Insecticidal Compounds from Persea indica

Gonzalez-Coloma A, Andrés MF, Contreras R, Zúñiga GE, Díaz CE

Plants (Basel)

03-Feb-2022

PMCID:	PMC8838882
doi:	10.3390/plants11030418
PMID:	35161399

Mechanisms of Action of Microbial Biocontrol Agents against Botrytis cinerea

Roca-Couso R, Flores-Félix JD, Rivas R

J Fungi (Basel)

06-Dec-2021

PMCID:	PMC8707566
doi:	10.3390/jof7121045
PMID:	34947027

Supercritical Antisolvent Fractionation of Antioxidant Compounds from Salvia officinalis

Mur R, Pardo JI, Pino-Otín MR, Urieta JS, Mainar AM

Int J Mol Sci

28-Aug-2021

PMCID:	PMC8431610
doi:	10.3390/ijms22179351
PMID:	34502255

Natural and Historical Heritage of the Lisbon Botanical Gardens: An Integrative Approach with Tree Collections

Cunha AR, Soares AL, Brilhante M, Arsénio P, Vasconcelos T, Espírito-Santo D, Duarte MC, Romeiras MM

Plants (Basel)

04-Jul-2021

PMCID:	PMC8309379
doi:	10.3390/plants10071367
PMID:	34371570

ROS and Oxidative Response Systems in Plants Under Biotic and Abiotic Stresses: Revisiting the Crucial Role of Phosphite Triggered Plants Defense Response

Mohammadi MA, Cheng Y, Aslam M, Jakada BH, Wai MH, Ye K, He X, Luo T, Ye L, Dong C, Hu B, Priyadarshani SV, Wang-Pruski G, Qin Y

Front Microbiol

01-Jul-2021

PMCID:	PMC8281016
doi:	10.3389/fmicb.2021.631318
PMID:	34276579

Biopesticide Encapsulation Using Supercritical CO2: A Comprehensive Review and Potential Applications

do Nascimento Junior DR, Tabernero A, Cabral Albuquerque EC, Vieira de Melo SA

Molecules

30-Jun-2021

PMCID:	PMC8272144
doi:	10.3390/molecules26134003
PMID:	34209179

Autochthonous Angiostrongylus cantonensis, Angiostrongylus vasorum and Aelurostrongylus abstrusus infections in native terrestrial gastropods from the Macaronesian Archipelago of Spain

Segeritz L, Cardona A, Taubert A, Hermosilla C, Ruiz A

Parasitol Res

28-Jun-2021

PMCID:	PMC8263545
doi:	10.1007/s00436-021-07203-x
PMID:	34180003

Exploring endophytes for in vitro synthesis of bioactive compounds similar to metabolites produced in vivo by host plants

Sharma H, Rai AK, Dahiya D, Chettri R, Nigam PS

AIMS Microbiol

26-May-2021

PMCID:	PMC8255908
doi:	10.3934/microbiol.2021012
PMID:	34250374

The Study of the Kinetics of Metalaxyl Accumulation and Dissipation in Durian (Durio zibethinus L.) Leaf Using High-Performance Liquid Chromatography (HPLC) Technique

Phetkhajone S, Pichakum A, Songnuan W

Plants (Basel)

06-Apr-2021

PMCID:	PMC8067542
doi:	10.3390/plants10040708
PMID:	33917640

Assessing the In Vitro Inhibitory Effects on Key Enzymes Linked to Type-2 Diabetes and Obesity and Protein Glycation by Phenolic Compounds of Lauraceae Plant Species Endemic to the Laurisilva Forest

Spínola V, Castilho PC

Molecules

01-Apr-2021

PMCID:	PMC8037948
doi:	10.3390/molecules26072023
PMID:	33916292

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
2-Hydroxy-3-methoxybenzoic acid	70140	Click to see COC1=CC=CC(=C1O)C(=O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid	7478	Click to see COC1=CC=C(C=C1)C(=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid	19	Click to see C1=CC(=C(C(=C1)O)O)C(=O)O	154.12	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron;phenoxide	20488062	Click to see [H+].C1=CC=C(C=C1)[O-]	94.11	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid	8215	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O	340.60	unknown	via CMAUP database
Hexacosanoic acid	10469	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	396.70	unknown	via CMAUP database
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2S,3S,6S,7R,9S,10S,11S,13R,14R)-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecane-2,6,9,11,13,14-hexol	101693754	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1O)O4)O)O)(C(C)C)O)C)O)C)O	384.50	unknown	https://doi.org/10.1021/JF9500593
(1R,6S,7R,9S,10S,11S,13R,14R)-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecane-2,6,9,11,13,14-hexol	137706047	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1O)O4)O)O)(C(C)C)O)C)O)C)O	384.50	unknown	https://doi.org/10.1021/JF9500593
(1R,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadec-3-en-2-one	101093085	Click to see CC1=CCC2(C3(CC4(C5(C(CC3(C5(C2(C1=O)O4)O)O)(C(C)C)O)C)O)C)O	380.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
(2,6,9,11,13,14-Hexahydroxy-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-12-yl) acetate	85235218	Click to see CC1CCC2(C3(CC4(C5(C(C(C3(C5(C2(C1O)O4)O)O)OC(=O)C)(C(C)C)O)C)O)C)O	442.50	unknown	https://doi.org/10.1021/JF9500593
[(1R,2R,3S,6S,7R,9S,10S,11S,13R,14R)-6,9,11,13,14-pentahydroxy-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-2-yl] acetate	101306938	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1OC(=O)C)O4)O)O)(C(C)C)O)C)O)C)O	426.50	unknown	https://doi.org/10.1021/JF9500593
[(1R,2R,3S,6S,7S,9S,10S,11S,12R,13S,14R)-2,6,9,11,13,14-hexahydroxy-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-12-yl] acetate	101693753	Click to see CC1CCC2(C3(CC4(C5(C(C(C3(C5(C2(C1O)O4)O)O)OC(=O)C)(C(C)C)O)C)O)C)O	442.50	unknown	https://doi.org/10.1021/JF9500593
3-Deoxyryanodol	75069470	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1O)O4)O)O)(C(C)C)O)C)O)C)O	384.50	unknown	https://doi.org/10.1021/JF9500593
3,7,10-Trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecane-2,6,9,11,12,13,14-heptol	14588812	Click to see CC1CCC2(C3(CC4(C5(C(C(C3(C5(C2(C1O)O4)O)O)O)(C(C)C)O)C)O)C)O	400.50	unknown	https://doi.org/10.1021/JF9500593
6,9,11,13,14-Pentahydroxy-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.01,6.07,13.010,14]pentadecan-2-one	73104216	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1=O)O4)O)O)(C(C)C)O)C)O)C)O	382.40	unknown	https://doi.org/10.1021/JF9500593
8,11,13-Abietatriene-3beta-ol	13996029	Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C	286.50	unknown	via CMAUP database
Cinnzeylanine	85379763	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1OC(=O)C)O4)O)O)(C(C)C)O)C)O)C)O	426.50	unknown	https://doi.org/10.1021/JF9500593
Cinnzeylanol	44559448	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1O)O4)O)O)(C(C)C)O)C)O)C)O	384.50	unknown	https://doi.org/10.1021/JF9500593
Cinnzeylanone	101693755	Click to see CC1CCC2(C3(CC4(C5(C(CC3(C5(C2(C1=O)O4)O)O)(C(C)C)O)C)O)C)O	382.40	unknown	https://doi.org/10.1021/JF9500593
Ryanodol	14588813	Click to see CC1CCC2(C3(CC4(C5(C(C(C3(C5(C2(C1O)O4)O)O)O)(C(C)C)O)C)O)C)O	400.50	unknown	https://doi.org/10.1016/0031-9422(92)83104-7 https://doi.org/10.1016/0031-9422(93)80016-L https://doi.org/10.1021/JF9500593
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Dihydrosolidagenone	101717490	Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C	318.40	unknown	via CMAUP database
Rotundifuran	9841926	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	362.50	unknown	via CMAUP database
Vitetrifolin B	15543011	Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	362.50	unknown	via CMAUP database
Vitetrifolin C	15543012	Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C	360.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
Garajonone	101093084	Click to see CC1CC23C(CC1=O)(C4(CC(O2)(C5(C3(C4(C(C5(C(C)C)O)OC(=O)C)O)O)C)O)C)O	440.50	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate	93317	Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C	196.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
gamma-Tocopherol	92729	Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O	416.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R,6S,7S,9S,10S,11S,13R,14S)-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-2,6,9,11,13,14-hexol	21672106	Click to see CC1CCC2(C1(C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O)O	384.50	unknown	https://doi.org/10.1021/NP970167E
(1R,2S,3R,6R,7R,9S,10S,11S,13S,14S)-3,7,10-Trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-6,9,14-triol	21672104	Click to see CC1CCC2(C1C3C4(C5C2(CC(C4(C(C5)C(C)C)C)(O3)O)C)O)O	336.50	unknown	https://doi.org/10.1021/NP970167E
(1R,2S,3R,6R,7S,9S,10S,11S,13R,14S)-3,7,10-trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-6,9,11,13,14-pentol	21672105	Click to see CC1CCC2(C1C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O	368.50	unknown	https://doi.org/10.1021/NP970167E
3,7,10-Trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-2,6,9,11,13,14-hexol	73820792	Click to see CC1CCC2(C1(C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O)O	384.50	unknown	https://doi.org/10.1021/NP970167E
3,7,10-Trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-6,9,11,13,14-pentol	73820791	Click to see CC1CCC2(C1C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O	368.50	unknown	https://doi.org/10.1021/NP970167E
3,7,10-Trimethyl-11-propan-2-yl-15-oxapentacyclo[7.5.1.02,6.07,13.010,14]pentadecane-6,9,14-triol	73820790	Click to see CC1CCC2(C1C3C4(C5C2(CC(C4(C(C5)C(C)C)C)(O3)O)C)O)O	336.50	unknown	https://doi.org/10.1021/NP970167E
Perseanol	44559454	Click to see CC1CCC2(C1(C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O)O	384.50	unknown	https://doi.org/10.1021/NP970167E
Vignaticol	44559450	Click to see CC1CCC2(C1C3C4(C5(C(CC4(C2(CC5(O3)O)C)O)(C(C)C)O)C)O)O	368.50	unknown	https://doi.org/10.1021/NP970167E
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerone	92785	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1R,4aS,5R,7aR)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate	51346123	Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O	466.40	unknown	via CMAUP database
6'-O-p-Hydroxybenzoylmussaenosidic acid	23955877	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)COC(=O)C4=CC=C(C=C4)O)O)O)O)O	496.50	unknown	via CMAUP database
Mussaenosidic acid	21633105	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	via CMAUP database
Negundoside	9935561	Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O	496.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2R,6R,7R,8S,11R,12R)-2,6,8,12-tetrahydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-en-14-one	162954764	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	366.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
(1R,2R,6R,7R,8S,11S)-2,6,8-trihydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-ene-12,14-dione	637209	Click to see CC1CCC2(C3(CC(=O)OC2(C1=O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	364.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
(1R,2R,6R,7R,8S)-2,6,8-trihydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-ene-12,14-dione	10808762	Click to see CC1CCC2(C3(CC(=O)OC2(C1=O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	364.40	unknown	via CMAUP database
(1R,2R,6R,8R,9S,12S,13R)-2,6,9,13-tetrahydroxy-3,8,12-trimethyl-4-propan-2-yl-14-oxatetracyclo[6.5.3.01,9.02,6]hexadec-3-en-15-one	162980184	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C(=C(CC4(C3)O)C(C)C)C)O)C)O	380.50	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
(1S,2R,6R,7R,8S,11S,12R)-2,6,8,12-tetrahydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-en-14-one	162954765	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	366.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
(1S,2R,6R,8S,11S,12R)-2,6,8,12-tetrahydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-en-14-one	163186632	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	366.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
2,6,8-Trihydroxy-3,7,11-trimethyl-4-propan-2-yl-13-oxatetracyclo[5.5.3.01,8.02,6]pentadec-3-ene-12,14-dione	78200734	Click to see CC1CCC2(C3(CC(=O)OC2(C1=O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	364.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
2,6,9,13-Tetrahydroxy-3,8,12-trimethyl-4-propan-2-yl-14-oxatetracyclo[6.5.3.01,9.02,6]hexadec-3-en-15-one	162980183	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C(=C(CC4(C3)O)C(C)C)C)O)C)O	380.50	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
Anhydrocinnzeylanine	131752069	Click to see CC1CCC2(C3(CC(=O)OC2(C1OC(=O)C)C4(C3(CC(=C4C)C(C)C)O)O)C)O	408.50	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
Anhydrocinnzeylanol	73099741	Click to see CC1CCC2(C3(CC(=O)OC2(C1O)C4(C3(CC(=C4C)C(C)C)O)O)C)O	366.40	unknown	https://doi.org/10.1016/S0031-9422(00)00376-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(5S,6R,8R,9R,10S)-6-Acetoxy-9,15-dihydroxylabda-13-ene-16-oic acid 16,15-lactone	10022565	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
(8alpha)-9,16-Dihydroxylabda-13-ene-15-oic acid gamma-lactone	102105798	Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C	320.50	unknown	via CMAUP database
Previtexilactone	21636179	Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
Vitexilactone	21636178	Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C	378.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-Epiursolic acid	7163177	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	via CMAUP database
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	via CMAUP database
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	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
[(1R,2R,4aalpha,5'E)-2alpha,5,5,8abeta-Tetramethyl-4beta-acetoxy-4',5'-dihydrospiro[decalin-1,2'(3'H)-furan]-5'-ylidene]acetic acid	101357917	Click to see CC1CC(C2C(CCCC2(C13CCC(=CC(=O)O)O3)C)(C)C)OC(=O)C	364.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
2-(1-Pentadecenyl)furan	11514626	Click to see CCCCCCCCCCCCCC=CC1=CC=CO1	276.50	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
2-(1-Tridecen-12-ynyl)furan	86136794	Click to see C#CCCCCCCCCCC=CC1=CC=CO1	244.37	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
2-[(1E)-trideca-1,12-dienyl]furan	11708580	Click to see C=CCCCCCCCCCC=CC1=CC=CO1	246.40	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
2-[(E)-tridec-1-en-12-ynyl]furan	101687157	Click to see C#CCCCCCCCCCC=CC1=CC=CO1	244.37	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
2-Pentadec-1-enylfuran	54061814	Click to see CCCCCCCCCCCCCC=CC1=CC=CO1	276.50	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
Furan, 2-(1,12-tridecadienyl)-	73069201	Click to see C=CCCCCCCCCCC=CC1=CC=CO1	246.40	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5S)-3-dodec-11-enylidene-5-(hydroxymethyl)oxolan-2-one	163057659	Click to see C=CCCCCCCCCCC=C1CC(OC1=O)CO	280.40	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
2H-Pyran-2-one, 3-(11-dodecenylidene)tetrahydro-5-hydroxy-, (E)-(-)-	124391	Click to see C=CCCCCCCCCCC=C1CC(OC1=O)CO	280.40	unknown	https://doi.org/10.1016/0031-9422(95)00518-8
Isoambreinolide	15559824	Click to see CC1CCC2C(CCCC2(C13CCC(=O)O3)C)(C)C	264.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1	11208535	Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C	290.40	unknown	via CMAUP database
Vitex norditerpenoid 2	11462191	Click to see CC1CC(C2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C)OC(=O)C	348.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin	5280441	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone	5379563	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC	374.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	via CMAUP database
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	via CMAUP database
chrysoplenol D	5280699	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC	360.30	unknown	via CMAUP database

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Persea indica

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