Relevant bibliographies by topics / Hyrtios erectus

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Hyrtios erectus'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Hyrtios erectus"

1

Kwon, Oh-Seok, Donghwa Kim, Chang-Kwon Kim, et al. "Cytotoxic Scalarane Sesterterpenes from the Sponge Hyrtios erectus." Marine Drugs 18, no. 5 (2020): 253. http://dx.doi.org/10.3390/md18050253.

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Twelve new sesterterpenes along with eight known sesterterpenes were isolated from the marine sponge Hyrtios erectus collected off the coast of Chuuk Island, the Federated State of Micronesia. Based upon a combination of spectroscopic and computational analyses, these compounds were determined to be eight glycine-bearing scalaranes (1–8), a 3-keto scalarane (9), two oxidized-furan-bearing scalaranes (10 and 11), and a salmahyrtisane (12). Several of these compounds exhibited weak antiproliferation against diverse cancer cell lines as well as moderate anti-angiogenesis activities. The antiproli
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2

Kaweetripob, Wirongrong, Chulabhorn Mahidol, Pittaya Tuntiwachwuttikul, Somsak Ruchirawat, and Hunsa Prawat. "Cytotoxic Sesterterpenes from Thai Marine Sponge Hyrtios erectus." Marine Drugs 16, no. 12 (2018): 474. http://dx.doi.org/10.3390/md16120474.

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Four sesterterpenes, erectusolides B, C, D, and seco-manoalide-25-methyl ether, two 2-furanone derivatives, erectusfuranones A and B, together with thirteen known sesterterpenes, (6Z)-neomanoalide-24-acetate, two diastereomers of 24-O-methylmanoalide, luffariolide B, manoalide, (6E)- and (6Z)-neomanoalide, seco-manoalide, scalarafuran, 12-acetylscalarolide, 12-epi-O-deacetyl-19-deoxyscalarin, 12-epi-scalarin, and 12-O-deacetyl-12-epi-scalarin, three indole alkaloids, 5-hydroxy-1H-indole-3-carbaldehyde, hyrtiosine A, and variabine B, and one norterpene, cavernosine were isolated from the marine
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3

Ashour, Mohamed A., Ehab S. Elkhayat, Rainer Ebel, RuAngelie Edrada, and Peter Proksch. "Indole alkaloid from the Red Sea sponge Hyrtios erectus." Arkivoc 2007, no. 15 (2007): 225–31. http://dx.doi.org/10.3998/ark.5550190.0008.f22.

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4

Faten A. S. Alsulaimany, Salma A.O. Saleh, Mahmoud A. Elfaky, and Sameh S. Elhady. "Anti-Helicobacter pylori Activity of Red Sea Hyrtios erectus sponge and micro-organisms Extracts." International Journal of Research in Pharmaceutical Sciences 11, no. 3 (2020): 4963–76. http://dx.doi.org/10.26452/ijrps.v11i3.2816.

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Helicobacter pylori were considered one of the most bacterial infections in the world. Recently, the resistance of antibiotic against H. pylori is increasing and hence, it is necessary to find new and natural effective agents. Marine organisms and microorganism produce complex secondary metabolites and some of these compounds are antimicrobials agents. This study aimed to provide preliminary data to determine if marine Hyrtios erectus sponge, actinomycetes, and fungi extracts can inhibit the growth of H. pylori. In this study, the methanol extracts of the three samples of Hyrtios erectus spong
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5

S. Elhady, Sameh, Alaa A. Bagalagel, Hanin A. Bogari, Safwat A. Ahmed, and Reem M. Diri. "New Bromoindole Alkaloid Isolated from the Marine Sponge Hyrtios erectus." HETEROCYCLES 96, no. 4 (2018): 749. http://dx.doi.org/10.3987/com-18-13869.

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6

Kaweetripob, Wirongrong, Chulabhorn Mahidol, Siriporn Wongbundit, Pittaya Tuntiwachwuttikul, Somsak Ruchirawat, and Hunsa Prawat. "Sesterterpenes and phenolic alkenes from the Thai sponge Hyrtios erectus." Tetrahedron 74, no. 2 (2018): 316–23. http://dx.doi.org/10.1016/j.tet.2017.11.073.

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7

Iguchi, Kazuo, Yoshie Shimada, and Yasuji Yamada. "Hyrtiosal, a new sesterterpenoid with a novel carbon skeleton from the Okinawan marine sponge Hyrtios erectus." Journal of Organic Chemistry 57, no. 2 (1992): 522–24. http://dx.doi.org/10.1021/jo00028a023.

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8

Elhady, Sameh, Ahmed Al-Abd, Ali El-Halawany, Abdulrahman Alahdal, Hashim Hassanean, and Safwat Ahmed. "Antiproliferative Scalarane-Based Metabolites from the Red Sea Sponge Hyrtios erectus." Marine Drugs 14, no. 7 (2016): 130. http://dx.doi.org/10.3390/md14070130.

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9

Alarif, Walied M., Sultan S. Al-Lihaibi, Mohamed A. Ghandourah, Mohamed I. Orif, Salim A. Basaif, and Seif-Eldin N. Ayyad. "Cytotoxic scalarane-type sesterterpenes from the Saudi Red Sea sponge Hyrtios erectus." Journal of Asian Natural Products Research 18, no. 6 (2015): 611–17. http://dx.doi.org/10.1080/10286020.2015.1115019.

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10

Elhady, Sameh, Ali El-Halawany, Abdulrahman Alahdal, Hashim Hassanean, and Safwat Ahmed. "A New Bioactive Metabolite Isolated from the Red Sea Marine Sponge Hyrtios erectus." Molecules 21, no. 1 (2016): 82. http://dx.doi.org/10.3390/molecules21010082.

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Dissertations / Theses on the topic "Hyrtios erectus"

1

Sauleau, Pierre. "Etude chimique et biologique de deux éponges marines de Mer Rouge : Lamellodysidea herbacea et Hyrtios erectus." Paris, Muséum national d'histoire naturelle, 2005. http://www.theses.fr/2005MNHN0027.

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Les travaux réalisés sur les éponges marines, Lamellodysidea herbacea et Hyrtios erectus récoltées en Mer Rouge, ont conduit à l'isolement de 21 molécules dont 13 originales. L'analyse détaillée des données spectrales de RMN à 1D et 2D, de masse, UV, IR et de cristallographie ont permis d'établir leurs structures et leurs configurations relatives ou absolues. L'extrait CH2Cl2 de l'éponge Lamellodysidea herbacea a permis l'identification de 8 nouveaux dérivés polychlorés de la pyrrolidinone en plus du dysidamide, des dysidamides B et C précédemment décrits. Le dysidamide a révélé une activité p
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