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Mansoa alliacea

Mansoa alliacea - 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 UUID6440274504db0644618636
Scientific name Mansoa alliacea
Authority (Lam.) A.H.Gentry
First published in Ann. Missouri Bot. Gard. 66: 782 (1979 publ. 1980)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pseudocalymma pachypus (K.Schum.) Sandwith Rec. Trav. Bot. Néerl. 34: 211 (1937)
Pseudocalymma alliaceum (Lam.) Sandwith Rec. Trav. Bot. Néerl. 34: 210 (1937)
Pseudocalymma sagotii (Bureau & K.Schum.) Sandwith Rec. Trav. Bot. Néerl. 34: 210 (1937)
Pachyptera alliacea (Lam.) A.H.Gentry Brittonia 25: 236 (1973)
Pseudocalymma sagotii var. macrocalyx (Sandwith) L.O.Williams Phytologia 25: 458 (1973)
Pseudocalymma alliaceum var. macrocalyx Sandwith Kew Bull. 8: 468 (1953 publ. 1954)
Anemopaegma pachypus K.Schum. Nat. Pflanzenfam. 4(3b): 215 (1894)
Adenocalymma alliaceum Miers Ann. Mag. Nat. Hist. , ser. 3, 7: 394 (1861)
Adenocalymma obovatum Urb. Repert. Spec. Nov. Regni Veg. 14: 307 (1916)
Adenocalymma pachypus Bureau & K.Schum. Fl. Bras. 8(2): 110 (1896)
Adenocalymma sagotii Bureau & K.Schum. Fl. Bras. 8(2): 110 (1896)
Bignonia alliacea Lam. Encycl. [J. Lamarck & al.] 1(2): 421. 1785 [1 Aug 1785]
Bignonia citrifolia Vitman Summa Pl. 3: 511 (1789)

Common names Top

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Language Common/alternative name
English garlicvine
English garlic vine
Spanish sacha de ajos
Arabic مانسوة ثومية
Bengali নীল-পারুল
Bengali পারুল লতা
Bengali রসুন্ধি
Bengali লতা-পারুল
Malayalam വെള്ളുള്ളിച്ചെടി
Marathi लसूण वेल (मानसोआ अलियासिया)
Punjab کاسنی ویل
Quechua ahus waska
Thai กระเทียมเถา
Chinese 蒜香藤

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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
    • Caribbean
      • Bahamas
      • Dominican Republic
      • Haiti
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000778999
UNII 5YWE11Y79T
USDA Plants MAAL13
Tropicos 3701394
INPN 630093
KEW urn:lsid:ipni.org:names:152672-2
The Plant List kew-317544
Open Tree Of Life 639521
NCBI Taxonomy 353996
IPNI 152672-2
iNaturalist 343814
GBIF 3172603
Freebase /m/0k0pcz1
EOL 486950
USDA GRIN 315387
Wikipedia Mansoa_alliacea

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
From Plant to Chemistry: Sources of Active Opioid Antinociceptive Principles for Medicinal Chemistry and Drug Design Turnaturi R, Piana S, Spoto S, Costanzo G, Reina L, Pasquinucci L, Parenti C Molecules 14-Oct-2023
PMCID:PMC10609244
doi:10.3390/molecules28207089
PMID:37894567
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Saussurea costus extract as bio mediator in synthesis iron oxide nanoparticles (IONPs) and their antimicrobial ability Al-brahim JS PLoS One 09-Mar-2023
PMCID:PMC9997948
doi:10.1371/journal.pone.0282443
PMID:36893115
A nuclear target sequence capture probe set for phylogeny reconstruction of the charismatic plant family Bignoniaceae Fonseca LH, Carlsen MM, Fine PV, Lohmann LG Front Genet 09-Jan-2023
PMCID:PMC9869424
doi:10.3389/fgene.2022.1085692
PMID:36699458
The Development of Pharmacophore Models for the Search of New Natural Inhibitors of SARS-CoV-2 Spike RBD–ACE2 Binding Interface Semenov VA, Krivdin LB Molecules 15-Dec-2022
PMCID:PMC9788546
doi:10.3390/molecules27248938
PMID:36558067
The Ethnographic Quest in the Midst of COVID-19 Abad Espinoza LG Int J Qual Methods 25-Oct-2022
PMCID:PMC9597281
doi:10.1177/16094069221135967
PMID:36317083
Greener synthesis of nanostructured iron oxide for medical and sustainable agro-environmental benefits Poh Yan L, Gopinath SC, Subramaniam S, Chen Y, Velusamy P, Chinni SV, Gobinath R, Lebaka VR Front Chem 20-Sep-2022
PMCID:PMC9533193
doi:10.3389/fchem.2022.984218
PMID:36212054
The Free Radical Scavenging Property of the Leaves, Branches, and Roots of Mansoa hirsuta DC: In Vitro Assessment, 3D Pharmacophore, and Molecular Docking Study Alves PE, Preet G, Dias L, Oliveira M, Silva R, Castro I, Silva G, Júnior J, Lima N, Silva DH, Andrade T, Jaspars M, Feitosa C Molecules 15-Sep-2022
PMCID:PMC9506257
doi:10.3390/molecules27186016
PMID:36144751
Exploring Foods of the Pacific: Cultural Food Identity in the US Affiliated Pacific Region Dela Cruz R, Wolfe E, Yonemori KM, Fialkowski MK, Wilkens LR, Coleman P, Lameko-Mua S, Johnson E, Gilmatam D, Sigrah C, Shomour M, Remengesau S, Alfred J, Acosta M, Ettienne R, Deenik J, Tanisha A, Salazar KA, Novotny R, Boushey CJ Hawaii J Health Soc Welf 01-Sep-2022
PMCID:PMC9460762
PMID:36118154
Diversity of endophytic fungal community in Huperzia serrata from different ecological areas and their correlation with Hup A content Pang B, Yin D, Zhai Y, He A, Qiu L, Liu Q, Ma N, Shen H, Jia Q, Liang Z, Wang D BMC Microbiol 05-Aug-2022
PMCID:PMC9354316
doi:10.1186/s12866-022-02605-y
PMID:35931950
Pharmacology and Phytochemistry of Ecuadorian Medicinal Plants: An Update and Perspectives Armijos C, Ramírez J, Salinas M, Vidari G, Suárez AI Pharmaceuticals (Basel) 11-Nov-2021
PMCID:PMC8624270
doi:10.3390/ph14111145
PMID:34832927
Migrant Pharmacopoeias: An Ethnobotanical Survey of Four Caribbean Communities in Amazonia (French Guiana) Tareau MA, Greene A, Palisse M, Odonne G Econ Bot 20-Oct-2021
PMCID:PMC8528477
doi:10.1007/s12231-021-09529-0
PMID:34697504
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
Assessment of biodiversity goods for the sustainable development of the chagra in an indigenous community of the Colombian Amazon: local values of crops Garavito G, Clavijo R, Luengas P, Palacios P, Arias MH J Ethnobiol Ethnomed 01-Apr-2021
PMCID:PMC8017740
doi:10.1186/s13002-021-00453-0
PMID:33794940
What’s in a name? Revisiting medicinal and religious plants at an Amazonian market Geertsma IP, Françozo M, van Andel T, Rodríguez MA J Ethnobiol Ethnomed 05-Feb-2021
PMCID:PMC7866673
doi:10.1186/s13002-021-00433-4
PMID:33546714

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 436.80 unknown https://doi.org/10.1006/BIOO.1993.1007
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown https://doi.org/10.1006/BIOO.1993.1007
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown https://doi.org/10.1006/BIOO.1993.1007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(32S)-32-hydroxyhexatriacontan-4-one 163188296 Click to see CCCCC(CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)CCC)O 537.00 unknown https://doi.org/10.1016/0031-9422(89)80147-5
(8R,34R)-34-hydroxy-8-methylheptatriacontan-5-one 163085638 Click to see CCCCC(=O)CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCC(CCC)O 565.00 unknown https://doi.org/10.1016/0031-9422(91)83723-X
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1006/BIOO.1993.1007
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1006/BIOO.1993.1007
32-Hydroxyhexatriacontan-4-one 14237689 Click to see CCCCC(CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)CCC)O 537.00 unknown https://doi.org/10.1016/0031-9422(89)80147-5
34-Hydroxy-8-methylheptatriacontan-5-one 14779585 Click to see CCCCC(=O)CCC(C)CCCCCCCCCCCCCCCCCCCCCCCCCC(CCC)O 565.00 unknown https://doi.org/10.1016/0031-9422(91)83723-X
Dotriacontanol 96117 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 466.90 unknown https://doi.org/10.1006/BIOO.1993.1007
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(17S)-pentatriacont-1-en-17-ol 162880162 Click to see CCCCCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCC=C)O 506.90 unknown https://doi.org/10.1016/0031-9422(91)83723-X
(19R)-19-hydroxyhexatriacontan-18-one 163044916 Click to see CCCCCCCCCCCCCCCCCC(C(=O)CCCCCCCCCCCCCCCCC)O 537.00 unknown https://doi.org/10.1016/0031-9422(89)80147-5
19-Hydroxyhexatriacontan-18-one 14237691 Click to see CCCCCCCCCCCCCCCCCC(C(=O)CCCCCCCCCCCCCCCCC)O 537.00 unknown https://doi.org/10.1016/0031-9422(89)80147-5
Pentatriacont-1-en-17-ol 14779583 Click to see CCCCCCCCCCCCCCCCCCC(CCCCCCCCCCCCCCC=C)O 506.90 unknown https://doi.org/10.1016/0031-9422(91)83723-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aS,6aS,6bS,8aS,10R,12aS,14bS)-10-hydroxy-2,2,4a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid 133611880 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C(=O)O)C)C 456.70 unknown https://doi.org/10.1055/S-2006-961437
30-Hydroxy-11-oxo-beta-amyrin 12310283 Click to see CC1(C2CCC3(C(C2(CCC1O)C)C(=O)C=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C 456.70 unknown https://doi.org/10.1055/S-2006-961437
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-((R,Z)-5-isopropylhept-5-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 134687892 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1006/BIOO.1993.1007
> Organoheterocyclic compounds / Dithiins
3-Vinyl-1,2-dithiacyclohex-4-ene 525328 Click to see C=CC1C=CCSS1 144.30 unknown https://doi.org/10.1021/JF00125A014
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(4S)-4-hydroxy-9-methoxy-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione 15735859 Click to see CC1(CC(C2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC)O)C 288.29 unknown https://doi.org/10.1016/0031-9422(92)80077-R
4-Hydroxy-9-methoxy-2,2-dimethyl-3,4-dihydrobenzo[g]chromene-5,10-dione 386660 Click to see CC1(CC(C2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC)O)C 288.29 unknown https://doi.org/10.1016/0031-9422(92)80077-R
9-Methoxy-alpha-lapachone 442754 Click to see CC1(CCC2=C(O1)C(=O)C3=C(C2=O)C=CC=C3OC)C 272.29 unknown https://doi.org/10.1016/0031-9422(92)80077-R
https://doi.org/10.1016/0031-9422(92)80223-2
> Organosulfur compounds / Allyl sulfur compounds
Allyl methyl disulfide 62434 Click to see CSSCC=C 120.20 unknown https://doi.org/10.1021/JF00125A014
Allyl methyl tetrasulfide 525329 Click to see CSSSSCC=C 184.40 unknown https://doi.org/10.1021/JF00125A014
Allyl propyl disulfide 16591 Click to see CCCSSCC=C 148.30 unknown https://doi.org/10.1021/JF00125A014
Diallyl disulfide 16590 Click to see C=CCSSCC=C 146.30 unknown https://doi.org/10.1021/JF00125A014
Diallyl sulfide 11617 Click to see C=CCSCC=C 114.21 unknown https://doi.org/10.1021/JF00125A014
Diallyl tetrasulfide 75552 Click to see C=CCSSSSCC=C 210.40 unknown https://doi.org/10.1021/JF00125A014
> Organosulfur compounds / Organic disulfides
3-Vinyl-4H-1,2-dithiin 150636 Click to see C=CC1CC=CSS1 144.30 unknown https://doi.org/10.1021/JF00125A014
Trithiacyclohexene 525332 Click to see C1CSSC=C1 118.20 unknown https://doi.org/10.1021/JF00125A014
> Organosulfur compounds / Organic trisulfides
Allyl methyl trisulfide 61926 Click to see CSSSCC=C 152.30 unknown https://doi.org/10.1021/JF00125A014
Allyl propyl trisulfide 525330 Click to see CCCSSSCC=C 180.40 unknown https://doi.org/10.1021/JF00125A014
Diallyl trisulfide 16315 Click to see C=CCSSSCC=C 178.30 unknown https://doi.org/10.1021/JF00125A014

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