Peperomia obtusifolia - Unknown
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Internal ID UUID6440019b0c138417868001
Scientific name Peperomia obtusifolia
Authority (L.) A.Dietr.
First published in Sp. Pl., ed. 6. 1: 154.

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Synonyms Top

Scientific name Authority First published in
Peperomia macropoda Miq. Linnaea 20: 128 (1847)
Peperomia puteolifera Trel. in Standl. Publ. Field Columb. Mus., Bot. Ser. 10: 157 (1931)
Peperomia cuneata Miq. London J. Bot. 4: 429 (1845)
Peperomia gollii Trel. in Standl. Publ. Field Columb. Mus., Bot. Ser. 10: 156 (1931)
Peperomia emarginata Ruiz & Pav. Fl. Peruv. [Ruiz & Pavon] 1: 33. t. 49. f. a. 1798
Piper hemionitidifolium D.Dietr. Syn. Pl. 1: 114 (1839)
Piper emarginatum Vahl Enum. Pl. 1: 339 (1804)
Piper obtusifolium L. Sp. Pl. : 30 (1753)
Piper tithymaloides Vahl Enum. Pl. 1: 340 (1804)
Peperomia magnoliifolia var. emarginulata C.DC. Prodr. 16(1): 427 (1869)
Peperomia obtusifolia var. emarginulata (C.DC.) C.DC. Bot. Jahrb. Syst. 40(3): 264. 1908 [24 Jan 1908]
Peperomia obtusifolia var. emarginata Dahlst. Kongl. Svenska Vetensk. Acad. Handl. , n.s., 33(2): 66 (1900)
Peperomia floridana Small Torreya 26: 109 (1926)
Peperomia cruciata Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 34 (1936)
Peperomia fieldiana Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 45 (1936)
Peperomia antoni var. reducta Trel. in Woodson & Schery Ann. Missouri Bot. Gard. 27: 299 (1940)
Peperomia bayatana Trel. Repert. Spec. Nov. Regni Veg. 23: 22, 30. 1926
Peperomia cuneifolia A.Dietr. Sp. Pl. ed. 6 , 1: 146 (1831)
Peperomia daiquiriana Trel. Repert. Spec. Nov. Regni Veg. 23: 30 (1926)
Peperomia dodecatheontophylla Trel. Contr. U.S. Natl. Herb. 26: 48 (1927)
Peperomia earlei Trel. Repert. Spec. Nov. Regni Veg. 23: 31. 1926
Peperomia hemionitidifolia Ham. Prodr. Pl. Ind. Occid. : 2 (1825)
Peperomia lunana Trel. Repert. Spec. Nov. Regni Veg. 23: 30 (1926)
Piper cuneifolium Jacq. Collectanea 4: 127 (1791)
Piper milleri Roem. & Schult. Syst. Veg., ed. 15 bis [Roemer & Schultes] 1: 337. 1817 [Jan-Jun 1817]
Rhynchophorum obtusifolium (L.) Small Man. S.E. Fl. [Small] 401. 1933 [30 Nov 1933]
Rhynchophorum floridanum (Small) Small Man. S.E. Fl. [Small] 401. 1933 [30 Nov 1933]
Peperomia valerioi Trel. J. Wash. Acad. Sci. 15: 458. 1925
Peperomia mentiens Trel. Contr. U.S. Natl. Herb. 26: 217 (1929)
Peperomia pyrolifolia Trel. Contr. U.S. Natl. Herb. 26: 217 (1929)
Peperomia palmae Trel. in Publ. Field Mus. Nat. Hist. Chicago, Bot. Ser. xviii. 320(1937).
Peperomia obtusifolia var. emarginulata (C.DC.) Trel. & Yunck. Piperac. N. South Amer. 2: 680–681, f. 596 1950
Piper humile Mill. Gard. Dict. ed. 8 : n.º 4 (1768)
Peperomia peninsularis Trel. Contr. U.S. Natl. Herb. 26: 216 (1929)
Peperomia galeottii Miq. Syst. Piperac. : 190 (1843)
Peperomia tithymaloides A.Dietr. Sp. Pl. ed. 6 , 1: 152 (1831)
Peperomia obtusifolia f. oblongifolia Miq. Fl. Bras. 4(1): 24 (1852)
Peperomia obtusifolia var. macropoda Dahlst. Kongl. Svenska Vetensk. Acad. Handl. , n.s., 33(2): 65 (1900)
Peperomia obtusifolia var. papyracea Griseb. Fl. Brit. W. I. : 166 (1859)
Peperomia obtusifolia var. petiolata Dahlst. Kongl. Svenska Vetensk. Acad. Handl. , n.s., 33(2): 67 (1900)
Peperomia obtusifolia var. floridana (Small) D.B.Ward Phytologia 94: 477 (2012)

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Language Common/alternative name
English baby rubberplant
Persian پپرومیا ابلق
Polish pieprzówka tępolistna
Chinese 圆叶椒草
Chinese 圓葉椒草
Chinese 花叶豆瓣绿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Peperomia obtusifolia var. alveolata (Trel.) Alain Brittonia 20: 160 (1968)
Peperomia obtusifolia var. cuneata (Miq.) Griseb. Fl. Brit. W. I. 166 1864

Subvarieties (abbr. subvar.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000477916
Florida Plant Atlas 516
USDA Plants PEOB2
Tropicos 25001097
INPN 447438
KEW urn:lsid:ipni.org:names:679269-1
The Plant List kew-2556304
Missouri Botanical Garden 285088
Observations.org 349951
NCBI Taxonomy 69414
Nature Serve 2.134039
IPNI 679270-1
iNaturalist 166493
GBIF 3086423
Freebase /m/0qb4p31
EPPO PEOOB
Elurikkus 365376
USDA GRIN 27341
Wikipedia Peperomia_obtusifolia
Open Tree Of Life 242356

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
Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus Moreno Cardenas C, Çiçek SS Front Microbiol 15-Aug-2023
PMCID:PMC10463185
doi:10.3389/fmicb.2023.1234115
PMID:37649631
Special Issue—“Isolation, Structure Elucidation and Biological Activity of Natural Products” Takahashi JA Molecules 14-Jul-2023
PMCID:PMC10383114
doi:10.3390/molecules28145392
PMID:37513264
Phytoremediation for the indoor environment: a state-of-the-art review Matheson S, Fleck R, Irga PJ, Torpy FR Rev Environ Sci Biotechnol 27-Feb-2023
PMCID:PMC9968648
doi:10.1007/s11157-023-09644-5
PMID:36873270
Antimicrobial properties and biotransforming ability of fungal endophytes from Ficus carica L. (Moraceae) Barolo MI, Castelli MV, López SN Mycology 17-Feb-2023
PMCID:PMC10161954
doi:10.1080/21501203.2023.2175500
PMID:37152850
Submerged leaves of live indoor foliage plants adsorb H1N1 influenza virus from suspension Song HJ, Yang SW, Jo JW, Choi YK, Lee IS, Lee BU, Lee SH, Kim HH, Kim KJ, Kim HJ Plant Signal Behav 12-Jan-2023
PMCID:PMC9851199
doi:10.1080/15592324.2022.2163869
PMID:36635991
Cross-School Collaboration to Develop and Implement Self-Construction Greening Systems for Schools Teichmann F, Kirchengast I, Korjenic A Plants (Basel) 10-Jan-2023
PMCID:PMC9860625
doi:10.3390/plants12020327
PMID:36679040
Monitoring of Indoor Farming of Lettuce Leaves for 16 Hours Using Electrical Impedance Spectroscopy (EIS) and Double-Shell Model (DSM) Nouaze JC, Kim JH, Jeon GR, Kim JH Sensors (Basel) 10-Dec-2022
PMCID:PMC9788501
doi:10.3390/s22249671
PMID:36560040
Bioactive Phenolic Compounds from Peperomia obtusifolia Ware I, Franke K, Hussain H, Morgan I, Rennert R, Wessjohann LA Molecules 07-Jul-2022
PMCID:PMC9315869
doi:10.3390/molecules27144363
PMID:35889234
Multi-Omics-Based Discovery of Plant Signaling Molecules Luo F, Yu Z, Zhou Q, Huang A Metabolites 13-Jan-2022
PMCID:PMC8777911
doi:10.3390/metabo12010076
PMID:35050197
Evaluation of Protection by Caffeic Acid, Chlorogenic Acid, Quercetin and Tannic Acid against the In Vitro Neurotoxicity and In Vivo Lethality of Crotalus durissus terrificus (South American Rattlesnake) Venom Oliveira IC, Yoshida EH, Dini MM, Paschoal AB, Cogo JC, da Cruz-Höfling MA, Hyslop S, Oshima-Franco Y Toxins (Basel) 13-Nov-2021
PMCID:PMC8623703
doi:10.3390/toxins13110801
PMID:34822584
Anti-trypanosomal screening of Salvadoran flora Castillo UG, Komatsu A, Martínez ML, Menjívar J, Núñez MJ, Uekusa Y, Narukawa Y, Kiuchi F, Nakajima-Shimada J J Nat Med 16-Sep-2021
PMCID:PMC8732892
doi:10.1007/s11418-021-01562-6
PMID:34529189
Biosynthesis of Pellucidin A in Peperomia pellucida (L.) HBK de Moraes MM, Kato MJ Front Plant Sci 22-Mar-2021
PMCID:PMC8020151
doi:10.3389/fpls.2021.641717
PMID:33828573
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969
Life Cycle-Based Host Range Analysis for Tomato Spotted Wilt Virus in Korea Kil EJ, Chung YJ, Choi HS, Lee S, Kim CS Plant Pathol J 01-Feb-2020
PMCID:PMC7012576
doi:10.5423/PPJ.FT.12.2019.0290
PMID:32089662

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 / Hydroxybenzoic acid derivatives
3,4-Dihydroxy-5-(3-methylbut-2-en-1-yl)benzoic acid 57339269 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)O)O)C 222.24 unknown https://doi.org/10.1080/14786410903244954
https://doi.org/10.1055/S-0029-1185364
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives
(2R)-5-hydroxy-2,7-dimethyl-8-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromene-6-carboxylic acid 636927 Click to see CC1=C(C2=C(CCC(O2)(C)C=CC=C(C)C)C(=C1C(=O)O)O)CC=C(C)C 370.50 unknown https://doi.org/10.1016/J.TETASY.2010.09.004
5-Hydroxy-2,7-dimethyl-8-(3-methylbut-2-enyl)-2-(4-methylpenta-1,3-dienyl)-3,4-dihydrochromene-6-carboxylic acid 73805517 Click to see CC1=C(C2=C(CCC(O2)(C)C=CC=C(C)C)C(=C1C(=O)O)O)CC=C(C)C 370.50 unknown https://doi.org/10.1055/S-0029-1185364
https://doi.org/10.1016/J.TETASY.2010.09.004
> Lignans, neolignans and related compounds / Furanoid lignans
1,4-Bis(3,4,5-trimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 99091 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1080/14786410903244954
Diayangambin 167452 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1080/14786410903244954
Episesartemin A 3732009 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1055/S-0029-1185364
EpisesarteminA 12697529 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1055/S-0029-1185364
Sesartemin 342737 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1055/S-0029-1185364
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
9-[[3-Hydroxy-4-[(7-hydroxy-4-methylhexadeca-3,5-dienoyl)amino]-2-methylbutanoyl]amino]nona-2,4,6-trienoic acid 73002902 Click to see CCCCCCCCCC(C=CC(=CCC(=O)NCC(C(C)C(=O)NCCC=CC=CC=CC(=O)O)O)C)O 546.70 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1080/14786410903244954
Corchoionoside C 10317980 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1080/14786410903244954
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Piperogalin 10336642 Click to see CC1=CC(=C(C(=C1CC=C(C)C)O)CC=C(C)CCC=C(C)C)O 328.50 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
8alpha-monoacetoxyphomadecalin D 132556713 Click to see CC1C(C=CC2=CC(C3(C(C12C)O3)C(=C)CO)OC(=O)C)O 306.40 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
> Organoheterocyclic compounds / Benzopyrans
(2R)-2,7-dimethyl-8-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromene-5,6-dione 163004757 Click to see CC1=C(C2=C(CCC(O2)(C)C=CC=C(C)C)C(=O)C1=O)CC=C(C)C 340.50 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(2R)-2,7-dimethyl-8-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromen-5-ol 163026954 Click to see CC1=CC(=C2CCC(OC2=C1CC=C(C)C)(C)C=CC=C(C)C)O 326.50 unknown https://doi.org/10.1016/J.TETASY.2010.09.004
(2S)-2,7-dimethyl-6-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromen-5-ol 163024638 Click to see CC1=CC2=C(CCC(O2)(C)C=CC=C(C)C)C(=C1CC=C(C)C)O 326.50 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
(2S)-2,7-dimethyl-8-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromen-5-ol 139248618 Click to see CC1=CC(=C2CCC(OC2=C1CC=C(C)C)(C)C=CC=C(C)C)O 326.50 unknown https://doi.org/10.1016/J.TETASY.2010.09.004
https://doi.org/10.1016/S0031-9422(97)01050-9
2,7-Dimethyl-6-(3-methylbut-2-enyl)-2-(4-methylpenta-1,3-dienyl)-3,4-dihydrochromen-5-ol 72761752 Click to see CC1=CC2=C(CCC(O2)(C)C=CC=C(C)C)C(=C1CC=C(C)C)O 326.50 unknown https://doi.org/10.1055/S-0029-1185364
2,7-dimethyl-6-(3-methylbut-2-enyl)-2-[(1E)-4-methylpenta-1,3-dienyl]-3,4-dihydrochromen-5-ol 100926761 Click to see CC1=CC2=C(CCC(O2)(C)C=CC=C(C)C)C(=C1CC=C(C)C)O 326.50 unknown https://doi.org/10.1016/S0031-9422(97)01050-9
https://doi.org/10.1055/S-0029-1185364
2,7-Dimethyl-8-(3-methylbut-2-enyl)-2-(4-methylpenta-1,3-dienyl)-3,4-dihydrochromen-5-ol 163026951 Click to see CC1=CC(=C2CCC(OC2=C1CC=C(C)C)(C)C=CC=C(C)C)O 326.50 unknown https://doi.org/10.1055/S-0029-1185364
https://doi.org/10.1016/J.TETASY.2010.09.004
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
7,4'-Di-O-methylvitexin 2''-O-rhamnoside 101458317 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)CO)O)O)O)O)O 606.60 unknown https://doi.org/10.1055/S-0029-1185364
https://doi.org/10.1080/14786410903244954
Isoswertisin 2''-rhamnoside 443901 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)OC)CO)O)O)O)O)O 592.50 unknown https://doi.org/10.1055/S-0029-1185364
https://doi.org/10.1080/14786410903244954
Isowertin 2''-rhamnoside 14427340 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)OC)CO)O)O)O)O)O 592.50 unknown https://doi.org/10.1055/S-0029-1185364
https://doi.org/10.1080/14786410903244954
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2'-Hydroxy-3-phenylpropiophenone 77052 Click to see C1=CC=C(C=C1)CCC(=O)C2=CC=CC=C2O 226.27 unknown https://doi.org/10.1016/S0031-9422(97)01050-9

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