Secondary Metabolites of Medicinal Plants. Bharat Singh

Чтение книги онлайн.

Читать онлайн книгу Secondary Metabolites of Medicinal Plants - Bharat Singh страница 53

Автор:
Жанр:
Серия:
Издательство:
Secondary Metabolites of Medicinal Plants - Bharat Singh

Скачать книгу

alt="Illustration of the tautomeric structures of hydroxyaloin A and cinnamoyl."/> Illustration of the tautomeric structures of hydroxyaloin B and deacetyllittoraloin. Illustration of the tautomeric structure of microdontin A/B. Illustration of the tautomeric structures of homonataloin and Nataloin A/B. Illustration of the tautomeric structures of Furanmethanol and Methylnaphto[2,3-c]furan. Illustration of the tautomeric structure of methylnaphto[2,3-c]furan-4, 9-dione. Illustration of the tautomeric structure of a diphenylethane derivative. Illustration of the tautomeric structures of Dihydrocoumarone, Methyl-p-coumarate, and Plicataloside. Illustration of the tautomeric structures of feroxidin and isoeleutherol. Illustration of the tautomeric structures of Pyrocatechol, Protocatechuic acid, and 8-C-Glucosyl-noreugenin. Illustration of the tautomeric structure of Coumaroyl. Illustration of the tautomeric structure of caffeoyl. Illustration of the tautomeric structures of 7-dihydroxychromone and Pluridone. Illustration of the tautomeric structures of 5-methylchromone and 7-hydroxy-5-methylchromone. Illustration of the tautomeric structure of feruloyl. Illustration of the tautomeric structures of Coumaroylaloesin and 5-dimethylchromone. Illustration of the tautomeric structure of trans-p-Cinnamoyl. Illustration of the tautomeric structure of cis- and trans-p-Coumaroyl. Illustration of the tautomeric structure of methylaloesin. Illustration of the tautomeric structure of 7-O-methylaloesinol. Illustration of the tautomeric structure of 2′-O-cinnamoyl. Illustration of the tautomeric structure of aloesol. Illustration of the tautomeric structure of p-coumaroyl – aloeresin A. Illustration of the tautomeric structures of aloeresin D and Aloeresin E. Illustration of the tautomeric structure of cinnamoyl – aloeresin E. Illustration of the tautomeric structures of Aloesol and Aloesone. Illustration of the tautomeric structures of Deacetylaloesin and Furoaloesone. Illustration of the tautomeric structures of Iso-aloeresin A and coumaroyl – Isoaloeresin D. Illustration of the tautomeric structures of Isoaloesin and Neoaloesin A. Illustration of the tautomeric structures of Caffeoyl – rabaichromone and Dihydroisocoumarin glucoside. Illustration of the tautomeric structures of Feralolide and CA-14. Illustration of the tautomeric structure of aloenin aglycone. Illustration of the tautomeric structures of Aloenin acetal and Ethylidenealoenin. Illustration of the tautomeric structure of p-coumaroyl – aloenin B. Illustration of the tautomeric structures of Bisbenzopyran and isovitexin. Illustration of the tautomeric structures of Dihydroisorhamnetin and Naringenin. Illustration of the tautomeric structures of Campesterol and Cholesterol. Illustration of the tautomeric structures of Lupeol and β-Sitosterol. Illustration of the tautomeric structures of Aloinoside A and Aloinoside B. Illustration of the tautomeric structures of ziganein and Cosmosiin. Illustration of the tautomeric structure of cycloartanol. Illustration of the tautomeric structure of Tetrahydroanthracene glucoside. Illustration of the tautomeric structures of Aloin A and 5-Hydroxyaloin. Illustration of the tautomeric structure of Microstigmin A. Illustration of the tautomeric structure of nataloin.

      The leaf as explant was cultured on MS, B5, and Schenk & Hidebrandt (SH) media supplemented with different combination of different NAA with BA and Kin for shoot induction. Maximum shoot induction rate observed in MS medium supplemented with NAA and BA in leaf explants (Sathyaprabha et al. 2010; Lakshmi and Padmaja 2011). Similarly maximum rooting was obtained on B5 medium supplemented with NAA and roots developed within 25 days after inoculation (Abdi et al. 2013). The exposure of dark period enhanced the production of 3,4-dihydro-2,4,8,9-tetrahydroxy-6-methyl-1(2H)-anthracenone-4-O-β-D-glucopyranoside and 3,4-dihydro-2-methoxy-4,8,9-trihydroxy-6-methyl-1(2H)-anthracenone-4-O-β-D-glucopyranoside in cell cultures of A. barbadensis (Yagi et al. 1998).

Скачать книгу