Cylindrolobus lindleyi

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Internal ID UUID68f8fcb1cce48694055648
Scientific name Cylindrolobus lindleyi
Authority (Thwaites) Ormerod & C.S.Kumar
First published in Harvard Pap. Bot. 23: 282 (2018)

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Scientific name Authority First published in
Pinalia lindlyei (Thwaites) Kuntze Revis. Gen. Pl. 2: 679 (1891)
Cylindrolobus bicolor Rauschert Feddes Repert. 94: 445 (1983)
Eria ephemera Rchb.f. Ann. Bot. Syst. 6: 272 (1861)
Dendrobium bicolor Lindl. Gen. Sp. Orchid. Pl. : 90 (1830)
Eria lindleyi Thwaites Enum. Pl. Zeyl. : 299 (1861)
Eria bicolor Lindl. J. Proc. Linn. Soc., Bot. 3: 58 (1858)

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Database ID/link to page
Tropicos 50027801
KEW urn:lsid:ipni.org:names:633829-1
The Plant List kew-71258
Open Tree Of Life 3979493
NCBI Taxonomy 2058705
IPNI 633829-1
iNaturalist 1229686
GBIF 2815553
EOL 1112026
World Flora Online wfo-0001354508
KEW urn:lsid:ipni.org:names:77202327-1
NCBI Taxonomy 2732813
IPNI 60478803-2
GBIF 11108263

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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
Structural modifications of plumieride isolated from Plumeria bicolor and the effect of these modifications on in vitro anticancer activity. Dobhal MP, Li G, Gryshuk A, Graham A, Bhatanager AK, Khaja SD, Joshi YC, Sharma MC, Oseroff A, Pandey RK J Org Chem 17-Sep-2004
doi:10.1021/JO0491408
PMID:15357574
Ferulic acid esters from Plumeria bicolor M Dobhal Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00006-0
Three dihydroanthracenones from Gasteria bicolor. Dagne E, Van Wyk BE, Mueller M, Steglich W Phytochemistry 01-Feb-1996
doi:10.1016/0031-9422(95)00704-0
PMID:8835456

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 / Anthracenes
(2S,4R)-2,4,9-trihydroxy-6-methoxy-8-methyl-3,4-dihydro-2H-anthracen-1-one 162881114 Click to see 288.29 unknown https://doi.org/10.1016/0031-9422(95)00704-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
methyl 4'-(1-hydroxyethyl)-5'-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[4a,7a-dihydro-1H-cyclopenta[c]pyran-7,2'-furan]-4-carboxylate 3453259 Click to see 470.40 unknown https://doi.org/10.1021/JO0491408
Plumieride 72319 Click to see CC(C1=CC2(C=CC3C2C(OC=C3C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)OC1=O)O 470.40 unknown https://doi.org/10.1021/JO0491408
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Isoplumericin 5281543 Click to see CC=C1C2C3(C=CC4C3C(O2)OC=C4C(=O)OC)OC1=O 290.27 unknown https://doi.org/10.1021/JO0491408
Methyl 3-ethylidene-2-oxo-3,3a,7a,9b-tetrahydro-2H,4aH-1,4,5-trioxadicyclopenta[a,hi]indene-7-carboxylate 533578 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(99)00006-0
https://doi.org/10.1021/JO0491408
Plumericin 5281545 Click to see 290.27 unknown https://doi.org/10.1021/JO0491408
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1021/JO0491408
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1021/JO0491408
alpha-Amyrin acetate 92842 Click to see 468.80 unknown https://doi.org/10.1021/JO0491408
Npc25529 293754 Click to see 468.80 unknown https://doi.org/10.1021/JO0491408
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
34-acetyloxytetratriacontyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 100978501 Click to see 729.10 unknown https://doi.org/10.1016/S0031-9422(99)00006-0
34-Acetyloxytetratriacontyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 163000420 Click to see 729.10 unknown https://doi.org/10.1016/S0031-9422(99)00006-0
34-hydroxytetratriacontyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 100978500 Click to see 687.10 unknown https://doi.org/10.1016/S0031-9422(99)00006-0
34-Hydroxytetratriacontyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162985259 Click to see 687.10 unknown https://doi.org/10.1016/S0031-9422(99)00006-0

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