Brandegea bigelovii

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Ethnobotanical Use

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Details Top

Internal ID	UUID64400dba3204c281689060
Scientific name	Brandegea bigelovii
Authority	(S.Watson) Cogn.
First published in	Proc. Calif. Acad. Sci. , ser. 2, 3: 58 (1890)

Ethnobotanical Use Top

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Synonyms Top

Scientific name	Authority	First published in
Vaseyanthus palmeri	(S.Watson) Gentry	Allan Hancock Pacific Exped. 13(2): 171 (1949)
Brandegea minima	(S.Watson) Rose	Contr. U.S. Natl. Herb. 5: 121. 1897
Brandegea monosperma	(Brandegee) Cogn.	Proc. Calif. Acad. Sci. , ser. 2, 3: 59 (1890)
Brandegea palmeri	(S.Watson) Rose	Contr. U.S. Natl. Herb. 5: 120 (1897)
Brandegea parviflora	(S.Watson) S.Watson ex Rose	Contr. U.S. Natl. Herb. 5: 120 (1897)
Cyclanthera monosperma	Brandegee	Proc. Calif. Acad. Sci. , ser. 2, 2: 159 (1889)
Echinocystis bigelovii	(S.Watson) Cogn.	Monogr. Phan. 3: 804 (1881)
Echinocystis brandegeei	Cogn.	Proc. Calif. Acad. Sci. ser. 2, 2: 215. 1889 ; et 3: 59 (1890)
Echinocystis parviflora	S.Watson	Proc. Amer. Acad. Arts 17: 373 (1882)
Echinopepon bigelovii	(S.Watson) S.Watson	Proc. Amer. Acad. Arts 24: 52 (1889)
Echinopepon palmeri	S.Watson	Proc. Amer. Acad. Arts 24: 52 (1889)
Echinopepon parviflorus	(S.Watson) S.Watson	Proc. Amer. Acad. Arts 24: 52 (1889)
Elaterium bigelovii	S.Watson	Proc. Amer. Acad. Arts 12: 252 (1877)
Vaseyanthus brandegeei	(Cogn.) Rose	Contr. U.S. Natl. Herb. 5: 119 (1897)
Vaseyanthus insularis var. palmeri	(S.Watson) Gentry	Madroño 10: 149 (1950)
Vaseyanthus insularis var. brandegeei	(Cogn.) I.M.Johnst.	Proc. Calif. Acad. Sci. , ser. 4, 12: 1182 (1924)

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Language	Common/alternative name
English	desert starvine

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Varieties (abbr. var.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

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- Extinct

- Introduced

- Native

Northern America click to expand
- Mexico
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southwest
- Southwestern U.S.A.
  - Arizona
  - California

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000570771
USDA Plants	BRBI
Tropicos	9200457
KEW	urn:lsid:ipni.org:names:36082-2
The Plant List	kew-2681865
Nature Serve	2.153079
IPNI	36082-2
iNaturalist	75866
GBIF	2874558
EOL	585693
Calflora (Californian flora)	1140
USDA GRIN	420187
CMAUP	NPO3614
Open Tree Of Life	760212

Genomes (via NCBI) Top

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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 / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(1,3-benzodioxol-5-ylmethyl)-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one	10523042	Click to see	368.40	unknown	via CMAUP database
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3,4-dimethoxyphenyl)methyl]-2H-furan-5-one	20056151	Click to see	384.40	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
3-[(R)-1,3-benzodioxol-5-yl(hydroxy)methyl]-4-[(3-hydroxy-4-methoxyphenyl)methyl]-2H-furan-5-one	21592358	Click to see	370.40	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see	138.16	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Chinensin	5315827	Click to see	364.30	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C	11796268	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
4-[(3S,3aS,6S,6aS)-6-(4-hydroxy-3,5-dimethoxy-phenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxy-phenol	12309695	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(-)-Matairesinol	119205	Click to see	358.40	unknown	via CMAUP database
(3R,4R)-3-(4-Hydroxy-3-methoxy-benzyl)-4-(4-hydroxy-3,5-dimethoxybenzyl)dihydrofuran-2(3H)-one	10249666	Click to see COC1=CC(=CC(=C1O)OC)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC	388.40	unknown	via CMAUP database
(3R,4R)-3-[(3,4-dimethoxyphenyl)methyl]-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	11164637	Click to see	372.40	unknown	via CMAUP database
(3R,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methyl]oxolan-2-one	101630410	Click to see COC1=C(C=C(C=C1)CC2C(COC2=O)CC3=CC4=C(C=C3)OCO4)O	356.40	unknown	via CMAUP database
(3R,4R)-4-[(3-hydroxy-4-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	101097988	Click to see	358.40	unknown	via CMAUP database
(3R,4R)-4-[(3,4-dihydroxyphenyl)methyl]-3-[(3,4-dimethoxyphenyl)methyl]oxolan-2-one	14682324	Click to see	358.40	unknown	via CMAUP database
(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-3-hydroxyoxolan-2-one	14630578	Click to see	386.40	unknown	via CMAUP database
(3S,4S)-3-hydroxy-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	101681939	Click to see	404.40	unknown	via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]oxolan-2-one	101630409	Click to see	354.40	unknown	via CMAUP database
(3Z,4R)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methylidene]oxolan-2-one	6506046	Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC	368.40	unknown	via CMAUP database
(3Z,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methylidene]oxolan-2-one	643806	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O	356.40	unknown	via CMAUP database
[(3R,4S)-4-(1,3-benzodioxol-5-ylmethyl)-3-[(3,4-dimethoxyphenyl)methyl]-2-oxooxolan-3-yl] acetate	14630580	Click to see CC(=O)OC1(C(COC1=O)CC2=CC3=C(C=C2)OCO3)CC4=CC(=C(C=C4)OC)OC	428.40	unknown	via CMAUP database
Arctigenin methyl ether	384877	Click to see	386.40	unknown	via CMAUP database
Arctigenin, (+)-	28125531	Click to see	372.40	unknown	via CMAUP database
Bursehernin	94504	Click to see	370.40	unknown	via CMAUP database
Epinortrachelogenin	14159539	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
Hydroxymatairesinol	10948757	Click to see	374.40	unknown	via CMAUP database
Isosalicifolin	638390	Click to see	356.40	unknown	via CMAUP database
Kaerophyllin	6440534	Click to see COC1=C(C=C(C=C1)C=C2C(COC2=O)CC3=CC4=C(C=C3)OCO4)OC	368.40	unknown	via CMAUP database
Nortrachelogenin	394846	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
Salicifolin	101681940	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2=CC3=CC(=C(C=C3)O)OC)O	356.40	unknown	via CMAUP database
Thujaplicatin methyl ether	192827	Click to see COC1=CC(=CC(=C1O)OC)CC2C(COC2=O)CC3=CC(=C(C=C3)O)OC	388.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(3R,3aR,6aR)-3-(1,3-benzodioxol-5-yl)-3,3a,4,6a-tetrahydro-1H-furo[3,4-c]furan-6-one	16038940	Click to see	248.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,6,7-Trimethoxycoumarin	148724	Click to see COC1=C(C(=C2C=CC(=O)OC2=C1)OC)OC	236.22	unknown	via CMAUP database
5,7-Dimethoxycoumarin	2775	Click to see	206.19	unknown	via CMAUP database
6,7,8-Trimethoxycoumarin	3083928	Click to see	236.22	unknown	via CMAUP database
Methylumbelliferone	10748	Click to see	176.17	unknown	via CMAUP database
Scoparone	8417	Click to see	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database

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Brandegea bigelovii

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top