Pachylobus normandii

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Scientific Literature

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Details Top

Internal ID	UUID644068c4a23ab449907725
Scientific name	Pachylobus normandii
Authority	(Aubrév. & Pellegr.) Byng & Christenh.
First published in	Global Fl. 0.259722222. 2018

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Dacryodes normandii	Aubrév. & Pellegr.	Fl. Gabon 3: 72 (1962)

Common names Top

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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

Africa click to expand
- West-central Tropical Africa
  - Congo
  - Equatorial Guinea
  - Gabon

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0001423920
KEW	urn:lsid:ipni.org:names:77183903-1
IPNI	77183903-1
iNaturalist	935839
GBIF	9723031
CMAUP	NPO14027
Open Tree Of Life	1086281

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

Seco ring-A triterpene acids from the resin of Dacryodes normandii

Ian C. Parsons, Alexander I. Gray, Peter G. Waterman, Catherine Lavaud, Georges Massiot

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)95205-1

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 / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)-	67179	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	via CMAUP database
Sabinene	10887971	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
beta-Cadinene	10657	Click to see CC1=CCC2C(C1)C(CC=C2C)C(C)C	204.35	unknown	via CMAUP database
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Copaene	12303902	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	via CMAUP database
delta-Cadinol	3084311	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(-)-Alloaromadendrene	10899740	Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C	204.35	unknown	via CMAUP database
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
Bicyclogermacrene	13894537	Click to see CC1=CCCC(=CC2C(C2(C)C)CC1)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(-)-Germacrene A	9548706	Click to see CC1=CCCC(=CCC(CC1)C(=C)C)C	204.35	unknown	via CMAUP database
Germacrene B	5281519	Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C	204.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	40469638	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
3-(1,4a,4b,6a,9,10-hexamethyl-8-oxo-2-prop-1-en-2-yl-3,4,5,6,7,9,10,10a,12,12a-decahydro-2H-chrysen-1-yl)propanoic acid	162912803	Click to see CC1C(C(=O)CC2(C1C3=CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)O)C(=C)C)C)C)C	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)95205-1
3-[(1S,2S,4aR,4bS,6aS,9S,10R,10aR,12aR)-1,4a,4b,6a,9,10-hexamethyl-8-oxo-2-prop-1-en-2-yl-3,4,5,6,7,9,10,10a,12,12a-decahydro-2H-chrysen-1-yl]propanoic acid	101606409	Click to see CC1C(C(=O)CC2(C1C3=CCC4C(C3(CC2)C)(CCC(C4(C)CCC(=O)O)C(=C)C)C)C)C	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)95205-1
CID 3003153	3003153	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C	470.70	unknown	via CMAUP database
Lantadene B	15560077	Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)(C)C)C	552.80	unknown	via CMAUP database
Lantanilic acid	101316804	Click to see CC(=CC(=O)OC1CC(CC2C1(CCC3(C2=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C)C(=O)O)(C)C)C	568.80	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 / Steroid acids
3-(1,4a,4b,6a,9,9-Hexamethyl-8-oxo-2-prop-1-en-2-yl-2,3,4,5,6,7,10,10a,12,12a-decahydrochrysen-1-yl)propanoic acid	163059088	Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(C(=O)C4)(C)C)C)C)C	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)95205-1
3-[(1S,2S,4aR,4bS,6aS,10aR,12aR)-1,4a,4b,6a,9,9-hexamethyl-8-oxo-2-prop-1-en-2-yl-2,3,4,5,6,7,10,10a,12,12a-decahydrochrysen-1-yl]propanoic acid	101606408	Click to see CC(=C)C1CCC2(C(C1(C)CCC(=O)O)CC=C3C2(CCC4(C3CC(C(=O)C4)(C)C)C)C)C	454.70	unknown	https://doi.org/10.1016/S0031-9422(00)95205-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin	5317284	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	via CMAUP database
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4',5-Dihydroxy-3',5',6,7-tetramethoxyflavone	16681753	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	374.30	unknown	via CMAUP database
5,3',4'-Trihydroxy-6,7,5'-trimethoxyflavone	14104185	Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	360.30	unknown	via CMAUP database
5,6-Dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-7-methoxychromen-4-one	91602946	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O	360.30	unknown	via CMAUP database
5,6-Dihydroxy-7,3',4'-Trimethoxyflavone	10020367	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC	344.30	unknown	via CMAUP database
Cirsiliol	160237	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC	330.29	unknown	via CMAUP database
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database
Fastigenin	162464	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	via CMAUP database
Nuchensin	373260	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O)O	330.29	unknown	via CMAUP database

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Pachylobus normandii

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top