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Rhizophora apiculata

Rhizophora apiculata - 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 UUID64404d69b9ef8359242364
Scientific name Rhizophora apiculata
Authority Blume
First published in Enum. Pl. Javae 1: 91 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhizophora candelaria DC. Prodr. 3: 32 (1828)

Common names Top

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Language Common/alternative name
English mangrove
Bengali গর্জন
Esperanto stretfolia rizoforo
Japanese フタバナヒルギ
Malayalam റൈസോഫെറാ എപ്പിക്കുലേറ്റ
Malayalam വള്ളിക്കണ്ടൽ
mnw ကင်တၞးဍောတ်၊ တၞံ
Malay pokok bakau minyak
Burmese ဗြူးခြေထောက်အဖို
Thai โกงกางใบเล็ก
Vietnamese Đước
Vietnamese cây đước
Chinese 紅樹
Chinese 正红树
Chinese 鸡笼答
Chinese 五足驴
Chinese 红树

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • Southwestern Pacific
      • Vanuatu

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001131596
UNII VPV95L835U
USDA Plants RHAP2
Tropicos 27600231
INPN 671456
KEW urn:lsid:ipni.org:names:719801-1
The Plant List tro-27600231
PaleoBotany 63218
Open Tree Of Life 242188
NCBI Taxonomy 106626
IUCN Red List 31382
IPNI 719801-1
iNaturalist 196660
GBIF 3086526
Freebase /m/02xcq7r
EPPO RHZAP
EOL 482361
USDA GRIN 105379
Wikipedia Rhizophora_apiculata

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_037832385.1 SYSU_Rhapic_HiC Chromosome Sun Yat-sen University 2024-04-01 59.0x 221.25 Mb

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
Profiling genome‐wide methylation in two maples: Fine‐scale approaches to detection with nanopore technology McEvoy SL, Grady PG, Pauloski N, O'Neill RJ, Wegrzyn JL Evol Appl 17-Apr-2024
PMCID:PMC11022628
doi:10.1111/eva.13669
PMID:38633133
Special Issue Editorial: “Antibacterial Agents from Natural Sources” Martins CH Molecules 30-Jan-2024
PMCID:PMC10856429
doi:10.3390/molecules29030644
PMID:38338388
The complete mitochondrial genome of the Kandelia obovata Sheue, H.Y.Liu & J.W.H.Yong (Rhizophoraceae) Xu X, Hou C, Shen Y Mitochondrial DNA B Resour 21-Dec-2023
PMCID:PMC10763820
doi:10.1080/23802359.2023.2294889
PMID:38173916
First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand Norphanphoun C, Hyde KD Pathogens 10-Dec-2023
PMCID:PMC10747506
doi:10.3390/pathogens12121436
PMID:38133319
Comparative chloroplast genome analyses provide insights into evolutionary history of Rhizophoraceae mangroves Zhang Y, Yang Y, He M, Wei Z, Qin X, Wu Y, Jiang Q, Xiao Y, Yang Y, Wang W, Jin X PeerJ 17-Nov-2023
PMCID:PMC10658886
doi:10.7717/peerj.16400
PMID:38025714
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Characterization of the complete chloroplast genome of Carallia brachiata (Lour.) Merr. (Rhizophoraceae) Zhou Y, She J, Jin C, Zhu X, Xiao F, Zhao J Mitochondrial DNA B Resour 16-Aug-2023
PMCID:PMC10435000
doi:10.1080/23802359.2023.2238935
PMID:37600503
Briquettes Made of Branches Wood of Three Mangrove Species Bonded by Starch Adhesive Tambunan H, Nuryawan A, Iswanto AH, Risnasari I, Basyuni M, Fatriasari W Materials (Basel) 27-Jul-2023
PMCID:PMC10420194
doi:10.3390/ma16155266
PMID:37569970
Research Progress of Nanomaterials in Chemotherapy of Osteosarcoma Yu T, Cai Z, Chang X, Xing C, White S, Guo X, Jin J Orthop Surg 05-Jul-2023
PMCID:PMC10475694
doi:10.1111/os.13806
PMID:37403654
CRISPR/Cas12a-based approaches for efficient and accurate detection of Phytophthora ramorum Guo Y, Xia H, Dai T, Liu T, Shamoun SF, CuiPing W Front Cell Infect Microbiol 27-Jun-2023
PMCID:PMC10333691
doi:10.3389/fcimb.2023.1218105
PMID:37441240
Comparative analysis of flavonoids, polyphenols and volatiles in roots, stems and leaves of five mangroves Wu Z, Shang X, Liu G, Xie Y PeerJ 22-Jun-2023
PMCID:PMC10290835
doi:10.7717/peerj.15529
PMID:37366424
Exploring the Xylariaceae and its relatives Suwannasai N, Sangvichien E, Phosri C, McCloskey S, Wangsawat N, Thamvithayakorn P, Ruchikachorn N, Thienhirun S, Mekkamol S, Sihanonth P, Whalley MA, Whalley AJ Bot Stud 14-Jun-2023
PMCID:PMC10310687
doi:10.1186/s40529-023-00389-6
PMID:37382773
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
Biosynthesis of Nanoparticles from Various Biological Sources and Its Biomedical Applications Karunakaran G, Sudha KG, Ali S, Cho EB Molecules 02-Jun-2023
PMCID:PMC10254633
doi:10.3390/molecules28114527
PMID:37299004
Red Mangrove (Rhizophora stylosa Griff.)—A Review of Its Botany, Phytochemistry, Pharmacological Activities, and Prospects Kalasuba K, Miranti M, Rahayuningsih SR, Safriansyah W, Syamsuri RR, Farabi K, Oktavia D, Alhasnawi AN, Doni F Plants (Basel) 01-Jun-2023
PMCID:PMC10255896
doi:10.3390/plants12112196
PMID:37299175

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 / Benzoic acids and derivatives / Benzoic acid esters
methyl 4-[(2S)-2-hydroxybut-3-ynoxy]benzoate 10976972 Click to see COC(=O)C1=CC=C(C=C1)OCC(C#C)O 220.22 unknown https://doi.org/10.1021/NP200885E
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown https://doi.org/10.1021/NP200885E
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Chloroisosulochrin 11100659 Click to see CC1=CC(=C(C(=C1)O)C(=O)C2=C(C(=C(C=C2C(=O)OC)OC)Cl)O)O 366.70 unknown https://doi.org/10.1021/NP200885E
Isosulochrin 16681742 Click to see CC1=CC(=C(C(=C1)O)C(=O)C2=C(C=C(C=C2O)OC)C(=O)OC)O 332.30 unknown https://doi.org/10.1021/NP200885E
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2-(3-chloro-2-hydroxy-4-methoxy-6-methoxycarbonyl-phenoxy)-6-hydroxy-4-methyl-benzoic Acid 9842980 Click to see CC1=CC(=C(C(=C1)OC2=C(C(=C(C=C2C(=O)OC)OC)Cl)O)C(=O)O)O 382.70 unknown https://doi.org/10.1021/NP200885E
Methyl 4-chloro-3-hydroxy-2-(3-hydroxy-5-methyl-phenoxy)-5-methoxy-benzoate 57342095 Click to see CC1=CC(=CC(=C1)OC2=C(C(=C(C=C2C(=O)OC)OC)Cl)O)O 338.74 unknown https://doi.org/10.1021/NP200885E
Pestalotether A 57342094 Click to see CC1=CC(=C(C(=C1)OC2=C(C(=C(C=C2C(=O)OC)OC)Cl)O)C(=O)OC)O 396.80 unknown https://doi.org/10.1021/NP200885E
Pestalotether C 101564922 Click to see CC1=CC(=C(C(=C1)OC2=C(C(=CC(=C2Cl)OC)C(=O)OC)O)C(=O)OC)O 396.80 unknown https://doi.org/10.1021/NP200885E
Pestalotether D 44715302 Click to see CC1=CC(=C(C(=C1)OC2=C(C=C(C=C2O)OC)C(=O)OC)C(=O)OC)O 362.30 unknown https://doi.org/10.1021/NP200885E
> Benzenoids / Phenols / Benzenediols / Hydroquinones
1,4-Benzenediol, 2-(3-methyl-3-buten-1-ynyl)- 189063 Click to see CC(=C)C#CC1=C(C=CC(=C1)O)O 174.20 unknown https://doi.org/10.1021/NP200885E
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heneicosanoic acid 16898 Click to see CCCCCCCCCCCCCCCCCCCCC(=O)O 326.60 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Hentriacontanoic acid 37982 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 466.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Heptacosanoic acid 23524 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 410.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Hexatriacontanoic acid 5282596 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 537.00 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Octacosanoic acid 10470 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Pentacosanoic acid 10468 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 382.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Tetratriacontanoic acid 94485 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 508.90 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Triacontanoic acid 10471 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 452.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Tritriacontanoic acid 181572 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 494.90 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hentriacontanol 68345 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 452.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
1-Nonacosanol 243696 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 424.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
1-Triacontanol 68972 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 438.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
3-(6-hydroxyheptyl)-4-methyl-2H-furan-5-one 11229606 Click to see CC1=C(COC1=O)CCCCCC(C)O 212.28 unknown https://doi.org/10.1021/NP200885E
Dotriacontanol 96117 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 466.90 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Seiridin 190634 Click to see CC1=C(COC1=O)CCCCCC(C)O 212.28 unknown https://doi.org/10.1021/NP200885E
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,8,10,10a-octahydrophenanthren-4-one 53496372 Click to see CC1(CCC(=O)C2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)C 320.50 unknown https://doi.org/10.1080/10286020.2011.589838
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP50070A026
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1080/10286020.2011.589838
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1080/10286020.2011.589838
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 314387 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1080/10286020.2011.589838
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Stellasterol 5283628 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C 398.70 unknown https://doi.org/10.1080/10286020.2011.589838
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/0031-9422(93)85036-Q
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3-(3-Methylbut-3-en-1-ynyl)-7-oxabicyclo[4.1.0]hept-3-ene-2,5-diol 14186847 Click to see CC(=C)C#CC1=CC(C2C(C1O)O2)O 192.21 unknown https://doi.org/10.1021/NP200885E
Asperpentyn 11480953 Click to see CC(=C)C#CC1=CC(C2C(C1O)O2)O 192.21 unknown https://doi.org/10.1021/NP200885E
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown https://doi.org/10.1016/0031-9422(93)85036-Q
> Organoheterocyclic compounds / Benzopyrans
Pestalochromone A 101564923 Click to see CC1(CC(=O)C2=C(O1)C(C(C(C2OC)O)O)Cl)C 276.71 unknown https://doi.org/10.1021/NP200885E
Pestalochromone B 101564924 Click to see CC1(CC(=O)C2=C(O1)C(C(C(C2OC)O)O)Cl)C 276.71 unknown https://doi.org/10.1021/NP200885E
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
2,2-Dimethyl-2H-chromene-6-carboxylic acid 5319235 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C(=O)O)C 204.22 unknown https://doi.org/10.1021/NP200885E
Pestalochromone C 57342264 Click to see CC1(CC(=O)C2=C(O1)C(=CC(=C2)O)Cl)C 226.65 unknown https://doi.org/10.1021/NP200885E
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Chloroisosulochrin dehydrate 11824253 Click to see CC1=CC(=C2C(=C1)OC3=C(C2=O)C(=CC(=C3Cl)OC)C(=O)OC)O 348.70 unknown https://doi.org/10.1021/NP200885E
Dehydroisosulochrin 101122392 Click to see CC1=CC(=C2C(=C1)OC3=CC(=CC(=C3C2=O)C(=O)OC)OC)O 314.29 unknown https://doi.org/10.1021/NP200885E
Pestaloxanthone 57342265 Click to see COC1=CC(=C2C(=C1)OC3=CC(=CC(=C3C2=O)O)CO)C(=O)OC 330.29 unknown https://doi.org/10.1021/NP200885E
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Pestalolide 57342266 Click to see CCCCCCCC1=C(C(=O)OC1)C 196.29 unknown https://doi.org/10.1021/NP200885E

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