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Internal ID UUID64400f188aa1f057637412
Scientific name Campylanthus glaber
Authority Benth.
First published in Prodr. 10: 508 (1846)

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Synonyms Top

Scientific name Authority First published in
Campylanthus benthamii Webb Niger Fl. [W. J. Hooker]. 163. 1849 [Nov-Dec 1849]
Campylanthus benthamii var. hirsutus Webb Hooker's Icon. Pl. 8: t. 776 1848
Campylanthus glaber var. puberulus Cout. Arq. Univ. Lisboa 1: 310 1914
Campylanthus glaber var. pumilus Pett. Commentat. Biol. 22(9): 43 1960
Campylanthus glaber subsp. spathulatus (A.Chev.) Brochmann, N.Kilian, Lobin & Rustan Sommerfeltia 24: 277 (1997)
Campylanthus spathulatus A.Chev. Rev. Bot. Appl. Agric. Trop. 15: 897 (1935)

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Distribution (via POWO/KEW) Top

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Database ID/link to page
World Flora Online wfo-0000583145
Tropicos 100304367
KEW urn:lsid:ipni.org:names:800758-1
The Plant List kew-2695410
Open Tree Of Life 68974
NCBI Taxonomy 554952
IUCN Red List 107423655
iNaturalist 506242
GBIF 7333177

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)!
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Title Authors Publication Released IDs
Characteristics, Isolation Methods, and Biological Properties of Aucubin Kartini K, Irawan MA, Setiawan F, Jayani NI Molecules 17-May-2023
PMCID:PMC10222036
doi:10.3390/molecules28104154
PMID:37241895
Diversity and biological activities of medicinal plants of Santiago island (Cabo Verde) Romeiras MM, Essoh AP, Catarino S, Silva J, Lima K, Varela E, Moura M, Gomes I, Duarte MC, Duarte MP Heliyon 21-Mar-2023
PMCID:PMC10060590
doi:10.1016/j.heliyon.2023.e14651
PMID:37009246
Multitarget in silico studies of Ocimum menthiifolium, family Lamiaceae against SARS-CoV-2 supported by molecular dynamics simulation Albohy A, Zahran EM, Abdelmohsen UR, Salem MA, Al-Warhi T, Al-Sanea MM, Abelyan N, Khalil HE, Desoukey SY, Fouad MA, Kamel MS J Biomol Struct Dyn 15-Dec-2020
PMCID:PMC7784784
doi:10.1080/07391102.2020.1852964
PMID:33317409
Patterns of genetic diversity in three plant lineages endemic to the Cape Verde Islands Romeiras MM, Monteiro F, Duarte MC, Schaefer H, Carine M AoB Plants 15-May-2015
PMCID:PMC4501515
doi:10.1093/aobpla/plv051
PMID:25979965
Iridoid glucosides and caffeoyl phenylethanoid glycosides from Campylanthus salsaloides and Campylanthus glaber Nina Rønsted, Søren Rosendal Jensen Elsevier BV 04-Nov-2002
doi:10.1016/S0305-1978(02)00061-3

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganic acid 158144 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
Melittoside 11968737 Click to see C1=COC(C2C1(C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 524.50 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
Monomelittoside 11968396 Click to see C1=COC(C2C1(C(C=C2CO)O)O)OC3C(C(C(C(O3)CO)O)O)O 362.33 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Gardoside 46173850 Click to see C=C1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 374.34 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[4-[4,5-dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate 131752795 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0305-1978(02)00061-3
Stachysoside A 14034195 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0305-1978(02)00061-3

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