Artocarpus gomezianus - Unknown
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Internal ID UUID64400aea2bc91067359494
Scientific name Artocarpus gomezianus
Authority Wall. ex Trécul
First published in Ann. Sci. Nat., Bot. , sér. 3, 8: 118 (1847)

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Synonyms Top

Scientific name Authority First published in
Saccus gomerianus Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus petiolaris Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Artocarpus masticatus Gagnep. Bull. Soc. Bot. France 73: 88 (1926)
Artocarpus petiolaris Miq. Fl. Ned. Ind., Eerste Bijv. : 422 (1861)
Artocarpus pomiformis Teijsm. & Binn. Natuurk. Tijdschr. Ned.-Indië 25: 400 (1863)
Artocarpus rigidus Wall. Numer. List : n.º 4658 (1831)

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Language Common/alternative name
Chinese 长圆叶波罗蜜

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000550486
Tropicos 50131969
KEW urn:lsid:ipni.org:names:850388-1
The Plant List kew-2653977
Open Tree Of Life 6107965
NCBI Taxonomy 1867283
IPNI 850388-1
iNaturalist 427961
GBIF 3764819
USDA GRIN 4328
Wikipedia Artocarpus_gomezianus

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
Efficacy of jackfruit components in prevention and control of human disease: A scoping review Tripathi K, Kumar P, Kumar R, Saxena R, Kumar A, Badoni H, Goyal B, Mirza AA J Educ Health Promot 31-Oct-2023
PMCID:PMC10743863
doi:10.4103/jehp.jehp_1683_22
PMID:38144022
Green Synthesis of Zinc Oxide (ZnO) Nanoparticles from Green Algae and Their Assessment in Various Biological Applications Hameed H, Waheed A, Sharif MS, Saleem M, Afreen A, Tariq M, Kamal A, Al-onazi WA, Al Farraj DA, Ahmad S, Mahmoud RM Micromachines (Basel) 25-Apr-2023
PMCID:PMC10224014
doi:10.3390/mi14050928
PMID:37241552
Biogenic Zinc Oxide Nanoparticles and Their Biomedical Applications: A Review Jha S, Rani R, Singh S J Inorg Organomet Polym Mater 20-Apr-2023
PMCID:PMC10118236
doi:10.1007/s10904-023-02550-x
PMID:37359387
Green synthesis of zinc oxide nanoparticles using Sea Lavender (Limonium pruinosum L. Chaz.) extract: characterization, evaluation of anti-skin cancer, antimicrobial and antioxidant potentials Naiel B, Fawzy M, Halmy MW, Mahmoud AE Sci Rep 27-Nov-2022
PMCID:PMC9701696
doi:10.1038/s41598-022-24805-2
PMID:36437355
Green synthesis of zinc oxide nanoparticles using Cocos nucifera leaf extract: characterization, antimicrobial, antioxidant and photocatalytic activity Rahman F, Majed Patwary MA, Bakar Siddique MA, Bashar MS, Haque MA, Akter B, Rashid R, Haque MA, Royhan Uddin AK R Soc Open Sci 23-Nov-2022
PMCID:PMC9682308
doi:10.1098/rsos.220858
PMID:36425517
Cycloartocarpin Inhibits Migration through the Suppression of Epithelial-to-Mesenchymal Transition and FAK/AKT Signaling in Non-Small-Cell Lung Cancer Cells Tungsukruthai S, Sritularak B, Chanvorachote P Molecules 22-Nov-2022
PMCID:PMC9737129
doi:10.3390/molecules27238121
PMID:36500213
Anoikis-Associated Lung Cancer Metastasis: Mechanisms and Therapies Wang J, Luo Z, Lin L, Sui X, Yu L, Xu C, Zhang R, Zhao Z, Zhu Q, An B, Wang Q, Chen B, Leung EL, Wu Q Cancers (Basel) 30-Sep-2022
PMCID:PMC9564242
doi:10.3390/cancers14194791
PMID:36230714
Green Synthesis and Characterization of ZnO Nanoparticles Using Pelargonium odoratissimum (L.) Aqueous Leaf Extract and Their Antioxidant, Antibacterial and Anti-inflammatory Activities Abdelbaky AS, Abd El-Mageed TA, Babalghith AO, Selim S, Mohamed AM Antioxidants (Basel) 26-Jul-2022
PMCID:PMC9329751
doi:10.3390/antiox11081444
PMID:35892646
Artonin F Induces the Ubiquitin-Proteasomal Degradation of c-Met and Decreases Akt-mTOR Signaling Soonnarong R, Putra ID, Sriratanasak N, Sritularak B, Chanvorachote P Pharmaceuticals (Basel) 21-May-2022
PMCID:PMC9145792
doi:10.3390/ph15050633
PMID:35631459
Exploring the Journey of Zinc Oxide Nanoparticles (ZnO-NPs) toward Biomedical Applications Islam F, Shohag S, Uddin MJ, Islam MR, Nafady MH, Akter A, Mitra S, Roy A, Emran TB, Cavalu S Materials (Basel) 15-Mar-2022
PMCID:PMC8951444
doi:10.3390/ma15062160
PMID:35329610
Green Nanotechnology: Plant-Mediated Nanoparticle Synthesis and Application Khan F, Shariq M, Asif M, Siddiqui MA, Malan P, Ahmad F Nanomaterials (Basel) 17-Feb-2022
PMCID:PMC8878231
doi:10.3390/nano12040673
PMID:35215000
Study on the Synthesis of ZnO Nanoparticles Using Azadirachta indica Extracts for the Fabrication of a Gas Sensor Acharya TR, Lamichhane P, Wahab R, Chaudhary DK, Shrestha B, Joshi LP, Kaushik NK, Choi EH Molecules 19-Dec-2021
PMCID:PMC8703601
doi:10.3390/molecules26247685
PMID:34946767
Plant-Mediated Zinc Oxide Nanoparticles: Advances in the New Millennium towards Understanding Their Therapeutic Role in Biomedical Applications Murali M, Kalegowda N, Gowtham HG, Ansari MA, Alomary MN, Alghamdi S, Shilpa N, Singh SB, Thriveni MC, Aiyaz M, Angaswamy N, Lakshmidevi N, Adil SF, Hatshan MR, Amruthesh KN Pharmaceutics 11-Oct-2021
PMCID:PMC8540056
doi:10.3390/pharmaceutics13101662
PMID:34683954
The complete chloroplast genome sequence of Artocarpus gomezianus (Moraceae) from Xishuangbanna, China Lin X, Lin T, Zhixia S, Priyadi A Mitochondrial DNA B Resour 09-Sep-2021
PMCID:PMC8439205
doi:10.1080/23802359.2021.1973603
PMID:34532580
Norcycloartocarpin targets Akt and suppresses Akt-dependent survival and epithelial-mesenchymal transition in lung cancer cells Nonpanya N, Sanookpan K, Joyjamras K, Wichadakul D, Sritularak B, Chaotham C, Chanvorachote P PLoS One 12-Aug-2021
PMCID:PMC8360371
doi:10.1371/journal.pone.0254929
PMID:34383763

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 / Naphthalenes
N-Phenyl-2-naphthylamine 8679 Click to see C1=CC=C(C=C1)NC2=CC3=CC=CC=C3C=C2 219.28 unknown https://doi.org/10.1055/S-2000-8656
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-[3-Hydroxy-5-methoxy-4-(3-methylbut-2-enyl)phenyl]-1-benzofuran-6-ol 15700061 Click to see CC(=CCC1=C(C=C(C=C1OC)C2=CC3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1016/S0367-326X(02)00210-1
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
2-[(1S)-1-(2,4-dihydroxyphenyl)-2-(3,5-dihydroxyphenyl)ethyl]-5-[(E)-2-(2,4-dihydroxyphenyl)ethenyl]benzene-1,3-diol 163036066 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=C(C(=C2)O)C(CC3=CC(=CC(=C3)O)O)C4=C(C=C(C=C4)O)O)O 488.50 unknown https://doi.org/10.1021/NP0101806
4-[(1S)-1-(2,4-dihydroxyphenyl)-2-(3,5-dihydroxyphenyl)ethyl]-6-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]benzene-1,3-diol 154496189 Click to see C1=CC(=C(C=C1O)O)C(CC2=CC(=CC(=C2)O)O)C3=C(C=C(C(=C3)C=CC4=CC(=CC(=C4)O)O)O)O 488.50 unknown https://doi.org/10.1021/NP0101806
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Norartocarpetin 5481970 Click to see C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown https://doi.org/10.1055/S-2000-8656
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Albanin A 5481961 Click to see CC(=CCC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O)C 354.40 unknown https://doi.org/10.1055/S-2000-8656
Artocarpin 5458461 Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)OC 436.50 unknown https://doi.org/10.1055/S-2000-8656
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Artocarpin (flavonoid); NSC 241010 44258292 Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)OC)C 436.50 unknown https://doi.org/10.1055/S-2000-8656
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Mulberrin 5481958 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)C 422.50 unknown https://doi.org/10.1007/S11418-006-0048-0
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(11S)-7,15-dihydroxy-19,19-dimethyl-11-(2-methylprop-1-enyl)-2,10,20-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(22),3(12),4(9),5,7,14,16(21),17-octaen-13-one 92448824 Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C 418.40 unknown https://doi.org/10.1055/S-2000-8656
(6S)-3,8-dihydroxy-10-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 163035062 Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC3C=C(C)C)OC 434.50 unknown https://doi.org/10.1055/S-2000-8656
3,8-dihydroxy-10-methoxy-9-(3-methylbut-1-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 5358261 Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC3C=C(C)C)OC 434.50 unknown https://doi.org/10.1055/S-2000-8656
3,8-dihydroxy-10-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 5458462 Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC3C=C(C)C)OC 434.50 unknown https://doi.org/10.1055/S-2000-8656
Cudraflavone A 5316261 Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=CC(O5)(C)C)C(=C4C2=O)O)C 418.40 unknown https://doi.org/10.1055/S-2000-8656
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1055/S-2000-8656
5-[(E)-2-(4-hydroxyphenyl)ethenyl]-3-methoxy-2-(3-methylbut-2-enyl)phenol 71626927 Click to see CC(=CCC1=C(C=C(C=C1OC)C=CC2=CC=C(C=C2)O)O)C 310.40 unknown https://doi.org/10.1016/S0367-326X(02)00210-1
5-[2-(4-Hydroxyphenyl)ethenyl]-3-methoxy-2-(3-methylbut-2-enyl)phenol 85517574 Click to see CC(=CCC1=C(C=C(C=C1OC)C=CC2=CC=C(C=C2)O)O)C 310.40 unknown https://doi.org/10.1016/S0367-326X(02)00210-1
CID 73197 73197 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/S0367-326X(02)00210-1
Oxyresveratrol 5281717 Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O 244.24 unknown https://doi.org/10.1016/S0367-326X(02)00210-1
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1055/S-2000-8656

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