Indigofera suffruticosa - Unknown
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Internal ID UUID643fdb6ab4eb8305576065
Scientific name Indigofera suffruticosa
Authority Mill.
First published in Gard. Dict. ed. 8: n.° 2 (1768)

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Synonyms Top

Scientific name Authority First published in
Indigofera tinctoria var. brachycarpa DC. Prodr.2: 224 (1825)
Indigofera micrantha Desv. Ann. Sci. Nat. (Paris)9: 410 (1826)
Indigofera guatimalensis Moc. & Sessé ex Prain & Baker f. J. Bot.40: 139 (1902)
Anil tinctoria var. brachycarpa (DC.) Kuntze Revis. Gen. Pl.1: 160 (1891)
Indigofera divaricata Jacq. Pl. Hort. Schoenbr.3: 61 (1798)
Indigofera guatimala Lunan Hort. Jamaic.1: 420 (1814)
Indigofera comezuelo DC.
Anila tinctoria var. vera Kuntze Revis. Gen. Pl. 1: 160. 1891 [5 Nov 1891]
Indigofera anil var. drepanocarpa O.Berg O.C.Berg & C.F.Schmidt, Darstell. Beschr. Off. Gew.4: 30d (1863)
Indigofera anil L. Mant. Pl.2: 272 (1771)
Indigofera tinctoria var. brachycarpa Vatke
Indigofera suffruticosa subsp. suffruticosa Mill. Blumea 30(1) 1984
Indigofera uncinata G.Don Gen. Hist.2: 208 (1832)
Indigofera angolensis D.Dietr. Syn. Plant.4: 1036 (1847)
Indigofera tinctoria var. anil (L.) Kurz
Indigofera suffruticosa var. uncinata Berhaut Fl. Senegal, ed. 2: 50 (1967)
Indigofera anil var. oligosperma Miq.
Ononis anil Mill. Gard. Dict. ed. 8: n.° 14 (1768)
Indigofera cornezuelo Moc. & Sessé ex DC. Prodr.2: 225 (1825)
Indigofera anil var. polyphylla DC. Prodr.2: 225 (1825)
Indigofera anil Sm. ex Wight & Arn. Prodr. Fl. Ind. Orient. 1: 202. 1834 [10 Oct 1834]
Indigofera anil var. drepanocarpa Berg Darst. Offiz. Gew. 4: 30d 1863
Indigofera suffruticosa f. obtusifolia Fawc. & Rendle Fl. Jamaica4: 16 (1920)
Indigofera suffruticosa subsp. guatemalensis (Moc. & Sessé ex Prain & Baker f.) de Kort & G.Thijsse Blumea30: 135 (1984)
Indigofera suffruticosa var. canescens (J.A.Schmidt) Lobin Courier Forschungsinst. Senckenberg81: 118 (1986)
Anil divaricata (Jacq.) Kuntze Revis. Gen. Pl.2: 939 (1891)
Anil tinctoria var. vera Kuntze Revis. Gen. Pl.1: 160 (1891)
Indigofera suffruticosa var. polyphylla DC. Prodr.2: 225 (1825)

Common names Top

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Language Common/alternative name
English anil de pasto
Arabic عظلم
Catalan anyil
Persian نیل وحشی
Irish ainil
Manx annyl
Japanese ナンバンコマツナギ
Lithuanian krūmokšninė indigažolė
Malayalam അമരി
pam tayum
Portuguese anileira
Portuguese Índigo
Quechua añil
Quechua tinaku
Thai ครามเถื่อน
Tonga ʻakauveli
Uzbek indigo yarim buta
Chinese 木蓝
Chinese 野青树
Chinese 野木藍
Chinese 假蓝靛
Chinese 雪人参

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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000195655
UNII 61XE6IT1XX
Florida Plant Atlas 392
USDA Plants INSU
Tropicos 13021076
INPN 629905
KEW urn:lsid:ipni.org:names:500063-1
The Plant List ild-4224
PFAF Indigofera suffruticosa
Open Tree Of Life 1026205
NCBI Taxonomy 100149
Nature Serve 2.141183
IPNI 30083265-2
iNaturalist 164064
GBIF 2971774
Freebase /m/0b_nwv
EOL 684285
USDA GRIN 20058
Wikipedia Indigofera_suffruticosa

Genomes (via NCBI) Top

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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
Indigofera suffruticosa aerial parts extract induce G2/M arrest and ATR/CHK1 pathway in Jurkat cells Tran HL, Lai KH, Chang HS, Chen YS, Wang HC, Yang SS, Chang HW, Hsu CM, Yen CH, Hsiao HH BMC Complement Med Ther 09-Jan-2024
PMCID:PMC10775588
doi:10.1186/s12906-023-04325-w
PMID:38195460
Effect of the Aqueous Extract of Chrysobalanus icaco Leaves on Maternal Reproductive Outcomes and Fetal Development in Wistar Rats Rodrigues NE, Oliveira AR, Lima SM, Nunes DM, de Albuquerque PB, da Cunha MD, Wanderley AG, Júnior FM, Silva JB, Teixeira ÁA, da Silva TG Curr Issues Mol Biol 19-Sep-2023
PMCID:PMC10529352
doi:10.3390/cimb45090479
PMID:37754263
A critical review of textile industry wastewater: green technologies for the removal of indigo dyes Castillo-Suárez LA, Sierra-Sánchez AG, Linares-Hernández I, Martínez-Miranda V, Teutli-Sequeira EA Int J Environ Sci Technol (Tehran) 27-Mar-2023
PMCID:PMC10041522
doi:10.1007/s13762-023-04810-2
PMID:37360556
Evidence synthesis of Chinese medicine for monkeypox: Suggestions from other contagious pox-like viral diseases Rong HG, Zhang XW, Han M, Sun X, Wu XD, Lai XZ, Shen C, Yu WJ, Fang H, Fei YT, Liu JP Front Pharmacol 13-Mar-2023
PMCID:PMC10040637
doi:10.3389/fphar.2023.1121580
PMID:36992826
A review on pathogenicity of Aeromonas hydrophila and their mitigation through medicinal herbs in aquaculture Semwal A, Kumar A, Kumar N Heliyon 28-Feb-2023
PMCID:PMC10018484
doi:10.1016/j.heliyon.2023.e14088
PMID:36938468
Plants causing poisoning outbreaks of livestock in South America: A review Riet-Correa F, Machado M, Micheloud JF Toxicon X 21-Jan-2023
PMCID:PMC9898795
doi:10.1016/j.toxcx.2023.100150
PMID:36747993
Potent Bioactivity of Endophytic Fungi Isolated from Moringa oleifera Leaves Rehman B, Khan SA, Hamayun M, Iqbal A, Lee IJ Biomed Res Int 15-Dec-2022
PMCID:PMC9779999
doi:10.1155/2022/2461021
PMID:36567913
A Critical Appraisal of the Most Recent Investigations on the Hepatoprotective Action of Brazilian Plants Garcia-Manieri JA, Correa VG, Backes E, de Sá-Nakanishi AB, Bracht L, Comar JF, Corrêa RC, Peralta RM, Bracht A Plants (Basel) 12-Dec-2022
PMCID:PMC9785989
doi:10.3390/plants11243481
PMID:36559593
Kaempferol: Antimicrobial Properties, Sources, Clinical, and Traditional Applications Periferakis A, Periferakis K, Badarau IA, Petran EM, Popa DC, Caruntu A, Costache RS, Scheau C, Caruntu C, Costache DO Int J Mol Sci 30-Nov-2022
PMCID:PMC9740324
doi:10.3390/ijms232315054
PMID:36499380
In vitro synergistic interaction between Melaleuca armillaris essential oil and erythromycin against Staphylococcus aureus isolated from dairy cows Buldain D, Gortari Castillo L, Buchamer AV, Bandoni A, Marchetti L, Mestorino N Front Vet Sci 15-Nov-2022
PMCID:PMC9705979
doi:10.3389/fvets.2022.1005616
PMID:36458057
Anaemia in Ruminants Caused by Plant Consumption Ruiz H, Lacasta D, Ramos JJ, Quintas H, Ruiz de Arcaute M, Ramo MÁ, Villanueva-Saz S, Ferrer LM Animals (Basel) 11-Sep-2022
PMCID:PMC9495094
doi:10.3390/ani12182373
PMID:36139233
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Indigofera tinctoria L. leaf powder promotes initiation of indigo reduction by inducing of rapid transition of the microbial community Lopes HD, Tu Z, Sumi H, Yumoto I Front Microbiol 09-Aug-2022
PMCID:PMC9395713
doi:10.3389/fmicb.2022.957809
PMID:36016790
A Multistage In Silico Study of Natural Potential Inhibitors Targeting SARS-CoV-2 Main Protease Elkaeed EB, Eissa IH, Elkady H, Abdelalim A, Alqaisi AM, Alsfouk AA, Elwan A, Metwaly AM Int J Mol Sci 29-Jul-2022
PMCID:PMC9369012
doi:10.3390/ijms23158407
PMID:35955547
Exploring the Phytochemicals and Anti-Cancer Potential of the Members of Fabaceae Family: A Comprehensive Review Usman M, Khan WR, Yousaf N, Akram S, Murtaza G, Kudus KA, Ditta A, Rosli Z, Rajpar MN, Nazre M Molecules 16-Jun-2022
PMCID:PMC9230627
doi:10.3390/molecules27123863
PMID:35744986

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 / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097430
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0028-1097430
> Organic 1,3-dipolar compounds / Allyl-type 1,3-dipolar organic compounds / Organic nitro compounds / C-nitro compounds
3-Nitropropionic acid 1678 Click to see C(C[N+](=O)[O-])C(=O)O 119.08 unknown https://doi.org/10.1016/S0305-1978(02)00087-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3-dihydroindol-2-one 162958517 Click to see C1=CC=C2C(=C1)C(C(=O)N2)OC3C(C(C(C(O3)CO)O)O)O 311.29 unknown https://doi.org/10.1080/14786419.2010.488624
Indican 441564 Click to see C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O 295.29 unknown https://doi.org/10.1080/14786419.2010.488624
Uroxanthin 258533 Click to see C1=CC=C2C(=C1)C(=CN2)OC3C(C(C(C(O3)CO)O)O)O 295.29 unknown https://doi.org/10.1080/14786419.2010.488624
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
Coronarian 441560 Click to see C(C[N+](=O)[O-])C(=O)OCC1C(C(C(C(O1)O)OC(=O)CC[N+](=O)[O-])O)O 382.28 unknown https://doi.org/10.1016/S0305-1978(02)00087-X
> Organoheterocyclic compounds / Azoles / Imidazoles
Allantoin 204 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1080/14786419.2010.488624
> Organoheterocyclic compounds / Azolidines / Imidazolidines / Hydantoins / Allantoins
(S)-(+)-allantoin 439714 Click to see C1(C(=O)NC(=O)N1)NC(=O)N 158.12 unknown https://doi.org/10.1080/14786419.2010.488624
> Organoheterocyclic compounds / Indoles and derivatives / Hydroxyindoles
Indigotine 135436515 Click to see C1=CC2=C(C=C1S(=O)(=O)O)C(=C(N2)C3=NC4=C(C3=O)C=C(C=C4)S(=O)(=O)O)O.[Na+] 445.40 unknown https://doi.org/10.1080/14786419.2010.488624
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(3Z)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one 5318433 Click to see C1=CC=C2C(=C1)C(=C3C(=O)C4=CC=CC=C4N3)C(=O)N2 262.26 unknown https://doi.org/10.1080/14786419.2010.488624
2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one 5464295 Click to see C1=CC=C2C(=C1)C(=O)C(=C3C(=O)C4=CC=CC=C4N3)N2 262.26 unknown https://doi.org/10.1080/14786419.2010.488624

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