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Caryodaphnopsis baviensis

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64400f851f6a1714095483
Scientific name Caryodaphnopsis baviensis
Authority (Lecomte) Airy Shaw
First published in Bull. Misc. Inform. Kew 1940: 76 (1940)

Description Top

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Synonyms Top

Scientific name Authority First published in
Persea baviensis (Lecomte) Kosterm. J. Sci. Res. (Jakarta) 1: 151 (1952)
Nothaphoebe baviensis Lecomte Nouv. Arch. Mus. Hist. Nat. sér. 5, 5: 107. 1913

Common names Top

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Language Common/alternative name
Vietnamese cà lồ ba vì
Chinese 巴围假檬果
Chinese 巴围檬果樟

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000588872
Tropicos 17802627
KEW urn:lsid:ipni.org:names:463181-1
The Plant List kew-2701886
Open Tree Of Life 6025616
IUCN Red List 172582665
IPNI 463181-1
GBIF 4180210
EOL 5400418

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)!
Title Authors Publication Released IDs
Neolignans from Caryodaphnopsis baviensis Nguyen Hoang Anh, Helmut Ripperger, Andrea Porzel, Tran Van Sung, Günter Adam Elsevier BV 13-May-2003
doi:10.1016/S0031-9422(97)00209-4

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
> Lignans, neolignans and related compounds / Furanoid lignans
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Icariside D1 13893575 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)(CO)O 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Phenylethanol + Hex-Pen 13893574 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)(CO)O 416.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2S)-1-(4-hydroxyphenyl)-2-[4-[(E)-prop-1-enyl]phenoxy]propan-1-one 163193944 Click to see CC=CC1=CC=C(C=C1)OC(C)C(=O)C2=CC=C(C=C2)O 282.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
1-(4-Hydroxyphenyl)-2-(4-prop-1-enylphenoxy)propan-1-one 85754270 Click to see CC=CC1=CC=C(C=C1)OC(C)C(=O)C2=CC=C(C=C2)O 282.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
> Organoheterocyclic compounds / Oxolanes
(3E,4S)-3-Hexadecylidenedihydro-4-hydroxy-5-methylene-2(3H)-furanone 44576045 Click to see CCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 336.50 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
3-Hexadecylidenedihydro-4-hydroxy-5-methylene-2(3h)-furanone 73200728 Click to see CCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 336.50 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Linderanolide 44576054 Click to see CCCCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 336.50 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(E)-3-[2-(1,3-benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]prop-2-enal 101936059 Click to see CC1=C(OC2=C1C=C(C=C2)C=CC=O)C3=CC4=C(C=C3)OCO4 306.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
2-Methoxy-4-[3-methyl-5-(1-propenyl)-2-benzofuranyl]-phenol 193821 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
3-[2-(1,3-Benzodioxol-5-yl)-3-methyl-1-benzofuran-5-yl]prop-2-enal 85754125 Click to see CC1=C(OC2=C1C=C(C=C2)C=CC=O)C3=CC4=C(C=C3)OCO4 306.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
4-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)phenol 3001232 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
4-(3-Methyl-5-prop-1-enyl-2,3-dihydro-1-benzofuran-2-yl)phenol 70414118 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
5-(3-Methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole 261729 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
5-(7-Methoxy-3-methyl-5-prop-1-enyl-1-benzofuran-2-yl)-1,3-benzodioxole 71436237 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC4=C(C=C3)OCO4 322.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
5-[3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole 6051545 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC4=C(C=C3)OCO4 292.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
5-[7-methoxy-3-methyl-5-[(E)-prop-1-enyl]-1-benzofuran-2-yl]-1,3-benzodioxole 5315032 Click to see CC=CC1=CC2=C(C(=C1)OC)OC(=C2C)C3=CC4=C(C=C3)OCO4 322.40 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Conocarpan 10999992 Click to see CC=CC1=CC2=C(C=C1)OC(C2C)C3=CC=C(C=C3)O 266.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Eupomatenoid 5 6443783 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC(=C(C=C3)O)OC 294.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4
Eupomatenoid 6 6261723 Click to see CC=CC1=CC2=C(C=C1)OC(=C2C)C3=CC=C(C=C3)O 264.30 unknown https://doi.org/10.1016/S0031-9422(97)00209-4

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