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Alluaudia humbertii

Alluaudia humbertii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64403875ec806005506638
Scientific name Alluaudia humbertii
Authority Choux
First published in Mém. Acad. Malgache 17: 30, 60 (1934)

Description Top

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Synonyms Top

Scientific name Authority First published in
Alluaudia decaryi Jacobs Handb. Sukk. Pfl. 1: 175 1954

Common names Top

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Language Common/alternative name
Chinese 七贤人
Chinese 亚蜡木
Chinese 细枝龙

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000943930
Tropicos 10700004
KEW urn:lsid:ipni.org:names:316433-1
The Plant List kew-6236
Missouri Botanical Garden 279837
Open Tree Of Life 369290
NCBI Taxonomy 86290
IPNI 316433-1
iNaturalist 480197
GBIF 5687103
EOL 6860121
USDA GRIN 444136
CMAUP NPO14434

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
CAM photosynthesis: the acid test Winter K, Smith JA New Phytol 05-Nov-2021
PMCID:PMC9298356
doi:10.1111/nph.17790
PMID:34637529
Essential Oil Composition of Alluaudia procera and in Vitro Biological Activity on Two Drug-Resistant Models Poma P, Labbozzetta M, Zito P, Alduina R, Ramarosandratana AV, Bruno M, Rosselli S, Sajeva M, Notarbartolo M Molecules 07-Aug-2019
PMCID:PMC6720003
doi:10.3390/molecules24162871
PMID:31394879
An efficient field and laboratory workflow for plant phylotranscriptomic projects Yang Y, Moore MJ, Brockington SF, Timoneda A, Feng T, Marx HE, Walker JF, Smith SA Appl Plant Sci 14-Mar-2017
PMCID:PMC5357122
doi:10.3732/apps.1600128
PMID:28337391
Competition for food in a solitarily foraging folivorous primate (Lepilemur leucopus)? Dröscher I, Kappeler PM Am J Primatol 26-Mar-2014
PMCID:PMC4229058
doi:10.1002/ajp.22272
PMID:24677259
6,8-Di-C-methyldihydromyricetin from Alluaudia humbertii Bernard Voirin, Richard Rasamoelisendra, Jean Favre-Bonvin, Marta Andriantsiferana, Zafera Rabesa Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)85532-6

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 / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
(5Z)-9,15-Dioxoprosta-5,8(12)-diene-1-oic acid methyl ester 21609756 Click to see CCCCCC(=O)CCC1=C(C(=O)CC1)CC=CCCCC(=O)OC 348.50 unknown via CMAUP database
methyl (Z)-7-[2-[(E,3S)-3-hydroxyoct-1-enyl]-5-oxocyclopenten-1-yl]hept-5-enoate 21160888 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)OC)O 348.50 unknown via CMAUP database
prostaglandin B2 5280881 Click to see CCCCCC(C=CC1=C(C(=O)CC1)CC=CCCCC(=O)O)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidonic Acid 444899 Click to see CCCCCC=CCC=CCC=CCC=CCCCC(=O)O 304.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
2-[(1R,4E,6E,10E,14R)-4,10,14-trimethyl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-trien-7-yl]propan-2-ol 23247586 Click to see CC1=CCCC2(C(O2)CCC(=CC=C(CC1)C(C)(C)O)C)C 304.50 unknown via CMAUP database
dimethyl (1S,4E,6Z,10Z,14S)-14-methyl-7-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-4,6,10-triene-4,10-dicarboxylate 16091634 Click to see CC(C)C1=CC=C(CCC2C(O2)(CCC=C(CC1)C(=O)OC)C)C(=O)OC 376.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Secogorgosterol 386853 Click to see CC(C)C(C)C1(CC1C(C)C2CCC(C2(C)CCO)C3CC=C4CC(CCC4(C3=O)C)O)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,2S,5E,7E)-2-acetyloxy-1-methyl-16-oxo-8-propan-2-yl-15-oxabicyclo[9.3.2]hexadeca-5,7,11-triene-5-carboxylate 16059808 Click to see CC(C)C1=CC=C(CCC(C2(CCC=C(CC1)C(=O)O2)C)OC(=O)C)C(=O)OC 404.50 unknown via CMAUP database
Sarcrassin E 16091635 Click to see CC(C)C1=CC=C(CCC(=O)C2(CCC=C(CC1)C(=O)O2)C)C(=O)OC 360.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones / Cembranolides
Crassocolide A 11995173 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)O)(C)O 392.50 unknown via CMAUP database
Crassocolide B 11995280 Click to see CC1=CCCC(C(CC2C(C(C(=CCC1)C)OC(=O)C)OC(=O)C2=C)OC(=O)C)(C)O 434.50 unknown via CMAUP database
Crassocolide C 11995174 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C)(C)O 376.50 unknown via CMAUP database
Crassocolide D 11995281 Click to see CC1=CCCC(C(CC2C(CC(=CCC1)C)OC(=O)C2=C)O)(C)O 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
25-Acetoxy-ergosta-3beta,5alpha,6beta-triol 14034721 Click to see CC(CCC(C)C(C)(C)OC(=O)C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 492.70 unknown via CMAUP database
5alpha-Ergostane-3beta,5,6beta-triol 44558918 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC(C4(C3(CCC(C4)O)C)O)O)C 434.70 unknown via CMAUP database
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 101007150 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22R,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007149 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 54586888 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)(C)O)OC1(C)C 444.60 unknown via CMAUP database
(22S,24S)-24-Methyl-22,25-epoxyfurosta-5-ene-3beta,20-diol 3-acetate 101007148 Click to see CC1CC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)(C)O)OC1(C)C 486.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Gorgostanes and derivatives
11alpha-Hydroxygorgosterol 10599347 Click to see CC(C)C(C)C1(CC1C(C)C2CCC3C2(CC(C4C3CC=C5C4(CCC(C5)O)C)O)C)C 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
24-Propylidenecholest-5-en-3beta-ol 193212 Click to see CCC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 426.70 unknown via CMAUP database
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans
(1R,2E,6R,8S,11E)-3,8,12,16-tetramethyl-7,18-dioxatricyclo[13.3.0.06,8]octadeca-2,11,15-triene 54585297 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(CO3)C)CC1)C)C 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Sarcocrassocolide A 70691856 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
Sarcocrassocolide B 70696020 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1OC(=O)C)OC(=O)C3=C)O)C 390.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2R,3R)-3,5,7-trihydroxy-6,8-dimethyl-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162970165 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=CC(=C(C(=C3)O)O)O)O)C)O 348.30 unknown https://doi.org/10.1016/S0031-9422(00)85532-6
3,5,7-Trihydroxy-6,8-dimethyl-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162970164 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=CC(=C(C(=C3)O)O)O)O)C)O 348.30 unknown https://doi.org/10.1016/S0031-9422(00)85532-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
6,8-Di-C-methylmyricetin 3-methyl ether 44259708 Click to see CC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)C)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)85532-6
> Phenylpropanoids and polyketides / Macrolides and analogues
(1aS,4E,8E,10aR,13aR,14aS)-4,8,14a-trimethyl-11-methylene-1a,3,6,7,10,10a,11,13a,14,14a-decahydrooxireno[12,13]cyclotetradeca[1,2-b]furan-12(2H)-one 643720 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,14S,15R)-14-hydroxy-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 21574172 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)O)OC(=O)C3=C)C 332.40 unknown via CMAUP database
(1R,3R,5R,8E,12E,15S)-5,9,13-trimethyl-18-methylidene-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-17-one 643718 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database
[(1R,3R,5R,8E,12E,14S,15R)-5,9,13-trimethyl-18-methylidene-17-oxo-4,16-dioxatricyclo[13.3.0.03,5]octadeca-8,12-dien-14-yl] acetate 21638415 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
13-Acetoxysarcocrassolide 21775908 Click to see CC1=CCCC2(C(O2)CC3C(C(C(=CCC1)C)OC(=O)C)OC(=O)C3=C)C 374.50 unknown via CMAUP database
Crassocolide E 11995175 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Crassocolide F 11995282 Click to see CC1=CCC(C(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C)OC(=O)C 374.50 unknown via CMAUP database
Crassocolide N 54764414 Click to see CC1=CCCC(=CC2C(CC3C(O3)(C(=O)CC1)C)C(=C)C(=O)O2)C 330.40 unknown via CMAUP database
ent-Sarcophine 101472593 Click to see CC1=CCCC2(C(O2)CCC(=CC3C(=C(C(=O)O3)C)CC1)C)C 316.40 unknown via CMAUP database
Lobophytolide 23425511 Click to see CC1=CCCC(=CCC2C(CC3(C(O3)CC1)C)OC(=O)C2=C)C 316.40 unknown via CMAUP database
Sarcocrassocolide C 46233394 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassocolide D 46233452 Click to see CC1=CCCC(=C)C2CCC(O2)(C(CC3C(C1)OC(=O)C3=C)O)C 332.40 unknown via CMAUP database
Sarcocrassolide 643719 Click to see CC1=CCCC2(C(O2)CC3C(CC(=CCC1)C)OC(=O)C3=C)C 316.40 unknown via CMAUP database

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