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Internal ID UUID643fdba7b70c7962623382
Scientific name Cicer cuneatum
Authority Hochst. ex A.Rich.
First published in Tent. Fl. Abyss.1: 195 (1847)

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Arabic حمص إسفيني

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
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • Northern Africa
      • Egypt

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000196646
Tropicos 13045577
KEW urn:lsid:ipni.org:names:486343-1
The Plant List ild-4321
Open Tree Of Life 192991
NCBI Taxonomy 92720
IPNI 486343-1
GBIF 2947295
EOL 685211
USDA GRIN 104849
CMAUP NPO29028

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
Exploring Chickpea Germplasm Diversity for Broadening the Genetic Base Utilizing Genomic Resourses Singh RK, Singh C, Ambika, Chandana BS, Mahto RK, Patial R, Gupta A, Gahlaut V, Gayacharan, Hamwieh A, Upadhyaya HD, Kumar R Front Genet 04-Aug-2022
PMCID:PMC9416867
doi:10.3389/fgene.2022.905771
PMID:36035111
A chickpea genetic variation map based on the sequencing of 3,366 genomes Varshney RK, Roorkiwal M, Sun S, Bajaj P, Chitikineni A, Thudi M, Singh NP, Du X, Upadhyaya HD, Khan AW, Wang Y, Garg V, Fan G, Cowling WA, Crossa J, Gentzbittel L, Voss-Fels KP, Valluri VK, Sinha P, Singh VK, Ben C, Rathore A, Punna R, Singh MK, Tar’an B, Bharadwaj C, Yasin M, Pithia MS, Singh S, Soren KR, Kudapa H, Jarquín D, Cubry P, Hickey LT, Dixit GP, Thuillet AC, Hamwieh A, Kumar S, Deokar AA, Chaturvedi SK, Francis A, Howard R, Chattopadhyay D, Edwards D, Lyons E, Vigouroux Y, Hayes BJ, von Wettberg E, Datta SK, Yang H, Nguyen HT, Wang J, Siddique KH, Mohapatra T, Bennetzen JL, Xu X, Liu X Nature 10-Nov-2021
PMCID:PMC8612933
doi:10.1038/s41586-021-04066-1
PMID:34759320
Current Perspectives on Introgression Breeding in Food Legumes Pratap A, Das A, Kumar S, Gupta S Front Plant Sci 21-Jan-2021
PMCID:PMC7858677
doi:10.3389/fpls.2020.589189
PMID:33552095
Breeding, Genetics, and Genomics Approaches for Improving Fusarium Wilt Resistance in Major Grain Legumes Jha UC, Bohra A, Pandey S, Parida SK Front Genet 23-Oct-2020
PMCID:PMC7644945
doi:10.3389/fgene.2020.01001
PMID:33193586
Legumes Protease Inhibitors as Biopesticides and Their Defense Mechanisms against Biotic Factors Rodríguez-Sifuentes L, Marszalek JE, Chuck-Hernández C, Serna-Saldívar SO Int J Mol Sci 08-May-2020
PMCID:PMC7246880
doi:10.3390/ijms21093322
PMID:32397104
Developing Climate-Resilient Chickpea Involving Physiological and Molecular Approaches With a Focus on Temperature and Drought Stresses Rani A, Devi P, Jha UC, Sharma KD, Siddique KH, Nayyar H Front Plant Sci 25-Feb-2020
PMCID:PMC7052492
doi:10.3389/fpls.2019.01759
PMID:32161601
Identification and Validation of Reference Genes and Their Impact on Normalized Gene Expression Studies across Cultivated and Wild Cicer Species Reddy DS, Bhatnagar-Mathur P, Reddy PS, Sri Cindhuri K, Sivaji Ganesh A, Sharma KK PLoS One 10-Feb-2016
PMCID:PMC4749333
doi:10.1371/journal.pone.0148451
PMID:26863232
The distribution of isoflavonoids in cicer Philip C. Stevenson, Nigel C. Veitch Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(97)00798-X

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
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
2-hydroxy-6-methoxy-9H-carbazole-3-carbaldehyde 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown via CMAUP database
2-Hydroxy-7-methoxy-9H-carbazole-3-carbaldehyde 189687 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)O 241.24 unknown via CMAUP database
2-Hydroxy-9H-carbazole-3-carbaldehyde 504068 Click to see C1=CC=C2C(=C1)C3=C(N2)C=C(C(=C3)C=O)O 211.22 unknown via CMAUP database
2-methoxy-9H-carbazol-3-ol 15182256 Click to see COC1=C(C=C2C3=CC=CC=C3NC2=C1)O 213.23 unknown via CMAUP database
2-methoxy-9H-carbazole-3-carbaldehyde 6483032 Click to see COC1=CC2=C(C=C1C=O)C3=CC=CC=C3N2 225.24 unknown via CMAUP database
7-Hydroxyheptaphylline 15767846 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)O)C=O)O)C 295.30 unknown via CMAUP database
7-methoxy-9H-carbazole-3-carbaldehyde 10537169 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=CC(=C3)C=O 225.24 unknown via CMAUP database
7-Methoxyheptaphylline 189688 Click to see CC(=CCC1=C(C(=CC2=C1NC3=C2C=CC(=C3)OC)C=O)O)C 309.40 unknown via CMAUP database
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown via CMAUP database
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown via CMAUP database
Clauraila D 51039828 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)C 293.30 unknown via CMAUP database
Clausenawalline G 71623800 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C(=CC(=C3)C(=O)OC)O)O)C 325.40 unknown via CMAUP database
Clausenawalline H 71623801 Click to see CC(=CCC1=C(C=CC2=C1C3=C(N2)C=C(C(=C3)C=O)O)O)C 295.30 unknown via CMAUP database
Clausenawalline I 71623858 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C=CC(=C4)C=O)C 277.30 unknown via CMAUP database
Clausenawalline K 71623860 Click to see CC1(C(C(C2=C(O1)C=CC3=C2C4=C(N3)C=C(C(=C4)C=O)O)O)O)C 327.30 unknown via CMAUP database
Clausine H 5315952 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)OC 285.29 unknown via CMAUP database
Clausine K 504070 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3N2)OC)C(=O)O 271.27 unknown via CMAUP database
Clauszoline N 101508363 Click to see C1=CC2=C(C=C1O)C3=C(N2)C=C(C(=C3)C=O)O 227.21 unknown via CMAUP database
Girinimbine 96943 Click to see CC1=CC2=C(C3=C1OC(C=C3)(C)C)NC4=CC=CC=C42 263.30 unknown via CMAUP database
Heptaphylline 5318015 Click to see CC(=CCC1=C(C(=CC2=C1NC3=CC=CC=C32)C=O)O)C 279.30 unknown via CMAUP database
Methyl 3-carbazolecarboxylate 504069 Click to see COC(=O)C1=CC2=C(C=C1)NC3=CC=CC=C32 225.24 unknown via CMAUP database
methyl 8-hydroxy-3,3-dimethyl-7H-pyrano[2,3-c]carbazole-10-carboxylate 71623859 Click to see CC1(C=CC2=C(O1)C=CC3=C2C4=C(N3)C(=CC(=C4)C(=O)OC)O)C 323.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1016/S0031-9422(97)00798-X

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