메뉴 건너뛰기




Volumn 74, Issue 12, 2009, Pages 927-930

3-Keto-22-epi-28-nor-cathasterone, a brassinosteroid-related metabolite from Cystoseira myrica

Author keywords

C27 brassinosteroid related; Cystoseira; Cytotoxicity

Indexed keywords

3 KETO 22 EPI 28 NOR CATHASTERONE; BRASSINOSTEROID; CHOLEST 4 ENE 3,6 DIONE; PLANT EXTRACT; UNCLASSIFIED DRUG;

EID: 69949190504     PISSN: 0039128X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.steroids.2009.06.008     Document Type: Article
Times cited : (31)

References (19)
  • 1
    • 0036053090 scopus 로고    scopus 로고
    • Brassinosteroids plant counterparts to animal steroid hormones?
    • Clouse S.D. Brassinosteroids plant counterparts to animal steroid hormones?. Vitam Horm 65 (2002) 195-223
    • (2002) Vitam Horm , vol.65 , pp. 195-223
    • Clouse, S.D.1
  • 2
    • 0037376236 scopus 로고    scopus 로고
    • The chemical characteristic and distribution of brassinosteroids in plants
    • Bajguz A., and Tretyn A. The chemical characteristic and distribution of brassinosteroids in plants. Phytochemistry 62 (2003) 1027-1046
    • (2003) Phytochemistry , vol.62 , pp. 1027-1046
    • Bajguz, A.1    Tretyn, A.2
  • 3
    • 0001094164 scopus 로고
    • Brassinosteroids and sterols from a green alga, Hydrodictyon reticulatum: configuration at C-24
    • Yokota T., Kim S.K., Fukui Y., Takahashi N., Takeuchi Y., and Takematsu T. Brassinosteroids and sterols from a green alga, Hydrodictyon reticulatum: configuration at C-24. Phytochemistry 26 (1987) 503-506
    • (1987) Phytochemistry , vol.26 , pp. 503-506
    • Yokota, T.1    Kim, S.K.2    Fukui, Y.3    Takahashi, N.4    Takeuchi, Y.5    Takematsu, T.6
  • 4
    • 30644459362 scopus 로고    scopus 로고
    • 3-Keto steroids from the marine organisms Dendrophyllia cornigera and Cymodocea nodosa
    • Kontiza I., Abatis D., Malakate K., Vagias C., and Roussis V. 3-Keto steroids from the marine organisms Dendrophyllia cornigera and Cymodocea nodosa. Steroids 71 (2006) 177-181
    • (2006) Steroids , vol.71 , pp. 177-181
    • Kontiza, I.1    Abatis, D.2    Malakate, K.3    Vagias, C.4    Roussis, V.5
  • 6
    • 0036800908 scopus 로고    scopus 로고
    • An early C-22 oxidation branch in the brassinosteroid biosynthetic pathway
    • Fujioka S., Takatsuto S., and Yoshida S. An early C-22 oxidation branch in the brassinosteroid biosynthetic pathway. Plant Physiol 130 (2002) 930-939
    • (2002) Plant Physiol , vol.130 , pp. 930-939
    • Fujioka, S.1    Takatsuto, S.2    Yoshida, S.3
  • 7
    • 0028894417 scopus 로고
    • Identification of a new brassinosteroid, cathasterone, in cultured cells of Catharanthus roseus as a biosynthetic precursor of teasterone
    • Fujioka S., Inoue T., Takatsuto S., Yanagisawa T., Yokota T., and Sakurai A. Identification of a new brassinosteroid, cathasterone, in cultured cells of Catharanthus roseus as a biosynthetic precursor of teasterone. Biosci Biotechnol Biochem 59 (1995) 1543-1547
    • (1995) Biosci Biotechnol Biochem , vol.59 , pp. 1543-1547
    • Fujioka, S.1    Inoue, T.2    Takatsuto, S.3    Yanagisawa, T.4    Yokota, T.5    Sakurai, A.6
  • 8
    • 0025201248 scopus 로고
    • Steroidal ketones from the sponge Geodia cydonium
    • Migliuolo A., Piccialli V., and Sica D. Steroidal ketones from the sponge Geodia cydonium. J Nat Prod 53 (1990) 1262-1266
    • (1990) J Nat Prod , vol.53 , pp. 1262-1266
    • Migliuolo, A.1    Piccialli, V.2    Sica, D.3
  • 9
    • 0034693489 scopus 로고    scopus 로고
    • 16β-Hydroxy-5α-cholestane-3,6-dione, a novel cytotoxic oxysterol from the red alga Jania rubens
    • Ktari L., Blond A., and Guyot M. 16β-Hydroxy-5α-cholestane-3,6-dione, a novel cytotoxic oxysterol from the red alga Jania rubens. Biorg Med Chem Lett 10 (2000) 2563-2565
    • (2000) Biorg Med Chem Lett , vol.10 , pp. 2563-2565
    • Ktari, L.1    Blond, A.2    Guyot, M.3
  • 10
    • 33845183935 scopus 로고
    • 2D-NMR Studies of a novel steroid from the red alga, Acantophora spicifera
    • Prakash O., Roy R., Bhakuni D.S., Wahidulla S., and Kamat S.Y. 2D-NMR Studies of a novel steroid from the red alga, Acantophora spicifera. J Nat Prod 52 (1989) 686-692
    • (1989) J Nat Prod , vol.52 , pp. 686-692
    • Prakash, O.1    Roy, R.2    Bhakuni, D.S.3    Wahidulla, S.4    Kamat, S.Y.5
  • 11
    • 0037042761 scopus 로고    scopus 로고
    • New ketosteroids from the red alga Hypnea musciformis
    • Bultel-Ponce V., Etahiri S., and Guyot M. New ketosteroids from the red alga Hypnea musciformis. Biorg Med Chem Lett 12 (2002) 1715-1718
    • (2002) Biorg Med Chem Lett , vol.12 , pp. 1715-1718
    • Bultel-Ponce, V.1    Etahiri, S.2    Guyot, M.3
  • 12
    • 0000040444 scopus 로고
    • 3-Dehydroteasterone, a 3 6-diketobrassinosteroid as a possible biosynthetic intermediate of brassinolide from wheat grain
    • Yokota T., Nakayama M., Wakisaka T., Schmidt J., and Adam G. 3-Dehydroteasterone, a 3 6-diketobrassinosteroid as a possible biosynthetic intermediate of brassinolide from wheat grain. Biosci Biotechnol Biochem 58 (1994) 1183-1185
    • (1994) Biosci Biotechnol Biochem , vol.58 , pp. 1183-1185
    • Yokota, T.1    Nakayama, M.2    Wakisaka, T.3    Schmidt, J.4    Adam, G.5
  • 14
    • 0035956411 scopus 로고    scopus 로고
    • A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR
    • Seco J.M., Quiñoá E., and Riguera R. A practical guide for the assignment of the absolute configuration of alcohols, amines and carboxylic acids by NMR. Tetrahedron Asymm 12 (2001) 2915-2925
    • (2001) Tetrahedron Asymm , vol.12 , pp. 2915-2925
    • Seco, J.M.1    Quiñoá, E.2    Riguera, R.3
  • 15
    • 0016864948 scopus 로고
    • Carbon-13 nuclear magnetic resonance of natural and related products XXII. Identification of C-22 epimers in steroids by carbon-13 nuclear magnetic resonance spectroscopy
    • Letourneux Y., Khuong-Huu Q., Gut M., and Kuckacs G. Carbon-13 nuclear magnetic resonance of natural and related products XXII. Identification of C-22 epimers in steroids by carbon-13 nuclear magnetic resonance spectroscopy. J Org Chem 40 (1975) 1674-1675
    • (1975) J Org Chem , vol.40 , pp. 1674-1675
    • Letourneux, Y.1    Khuong-Huu, Q.2    Gut, M.3    Kuckacs, G.4
  • 16
    • 0001981048 scopus 로고
    • Stereospecific synthesis of the 4 epimers of 7 22-dihydroxycholesterol
    • Amann A., Ourisson G., and Luu B. Stereospecific synthesis of the 4 epimers of 7 22-dihydroxycholesterol. Synthesis (1987) 1002-1005
    • (1987) Synthesis , pp. 1002-1005
    • Amann, A.1    Ourisson, G.2    Luu, B.3
  • 17
    • 0025063395 scopus 로고
    • Methylation and hydroxymethylation of allylic alcohols via radical cyclization. Methodology for stereoselective construction of an aliphatic chain in application to sterol synthesis
    • Kurek-Tyrlik A., Wicha J., and Zarecki A. Methylation and hydroxymethylation of allylic alcohols via radical cyclization. Methodology for stereoselective construction of an aliphatic chain in application to sterol synthesis. J Org Chem 55 (1990) 3484-3492
    • (1990) J Org Chem , vol.55 , pp. 3484-3492
    • Kurek-Tyrlik, A.1    Wicha, J.2    Zarecki, A.3
  • 18
    • 0002480922 scopus 로고    scopus 로고
    • Sakurai A., Yokota T., and Clouse S.D. (Eds), Springer, Tokyo, Japan
    • Sakurai A., and Biosynthesis. In: Sakurai A., Yokota T., and Clouse S.D. (Eds). Brassinosteroids-steroidal plant hormones (1999), Springer, Tokyo, Japan 91-111
    • (1999) Brassinosteroids-steroidal plant hormones , pp. 91-111
    • Sakurai, A.1    Biosynthesis2
  • 19
    • 33644852189 scopus 로고    scopus 로고
    • Arabidopsis CYP90B1 catalyses the early C-22 hydroxylation of C27, C28 and C29 sterols
    • Fujita S., Ohnishi T., Watanabe B., Yokota T., Takatsuto S., Fujioka S., et al. Arabidopsis CYP90B1 catalyses the early C-22 hydroxylation of C27, C28 and C29 sterols. Plant J 45 (2006) 765-774
    • (2006) Plant J , vol.45 , pp. 765-774
    • Fujita, S.1    Ohnishi, T.2    Watanabe, B.3    Yokota, T.4    Takatsuto, S.5    Fujioka, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.