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1
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1842580619
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Part 6:
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Part 6:. Saito N., Tanaka C., Koizumi Y., Suwanborirux K., Amnuoypol S., Pummangura S., and Kubo A. Tetrahedron 60 (2004) 3873-3881
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(2004)
Tetrahedron
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Saito, N.1
Tanaka, C.2
Koizumi, Y.3
Suwanborirux, K.4
Amnuoypol, S.5
Pummangura, S.6
Kubo, A.7
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3
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0036300526
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Suwanborirux K., Charupant K., Amnuoypol S., Pummangura S., Kubo A., and Saito N. J. Nat. Prod. 65 (2002) 935-937
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(2002)
J. Nat. Prod.
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, pp. 935-937
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Suwanborirux, K.1
Charupant, K.2
Amnuoypol, S.3
Pummangura, S.4
Kubo, A.5
Saito, N.6
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4
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0344118694
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Suwanborirux K., Amnuoypol S., Plubrukarn A., Pummangura S., Kubo A., Tanaka C., and Saito N. J. Nat. Prod. 66 (2003) 1441-1448
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(2003)
J. Nat. Prod.
, vol.66
, pp. 1441-1448
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Suwanborirux, K.1
Amnuoypol, S.2
Plubrukarn, A.3
Pummangura, S.4
Kubo, A.5
Tanaka, C.6
Saito, N.7
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5
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3042675982
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Amnuoypol S., Suwanborirux K., Pummangura S., Kubo A., Tanaka C., and Saito N. J. Nat. Prod. 67 (2004) 1023-1028
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(2004)
J. Nat. Prod.
, vol.67
, pp. 1023-1028
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Amnuoypol, S.1
Suwanborirux, K.2
Pummangura, S.3
Kubo, A.4
Tanaka, C.5
Saito, N.6
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6
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33846113891
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Charupant K., Suwanborirux K., Amnuoypol S., Saito E., Kubo A., and Saito N. Chem. Pharm. Bull. 55 (2007) 81-86
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(2007)
Chem. Pharm. Bull.
, vol.55
, pp. 81-86
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Charupant, K.1
Suwanborirux, K.2
Amnuoypol, S.3
Saito, E.4
Kubo, A.5
Saito, N.6
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7
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0025070774
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Ecteinascidin 770 is the stable form of ecteinascidin 743, a compound first reported by Reinhart et al. in 1990. See:
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Ecteinascidin 770 is the stable form of ecteinascidin 743, a compound first reported by Reinhart et al. in 1990. See:. Rinehart K.L., Holt T.G., Fregeau N.L., Stroh J.G., Kieffer P.A., Sun F., Li L.H., Martin D.G. J. Org. Chem. 55 (1990) 4512-4515
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(1990)
J. Org. Chem.
, vol.55
, pp. 4512-4515
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Rinehart, K.L.1
Holt, T.G.2
Fregeau, N.L.3
Stroh, J.G.4
Kieffer, P.A.5
Sun, F.6
Li, L.H.7
Martin, D.G.8
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8
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0024995421
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Wright A.E., Forleo D.A., Gunawardana G.P., Gunasekera S.F., and McConnel O.J. J. Org. Chem. 55 (1990) 4508-4512
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(1990)
J. Org. Chem.
, vol.55
, pp. 4508-4512
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Wright, A.E.1
Forleo, D.A.2
Gunawardana, G.P.3
Gunasekera, S.F.4
McConnel, O.J.5
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9
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0024818627
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Renieramycin M is the stable form of renieramycin E, a compound that was isolated in a minute amount marine natural product from the methanol extract of the blue sponge Reniera sp. inhabiting a small marine lake in Urukhapel Island, Palau. See:
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Renieramycin M is the stable form of renieramycin E, a compound that was isolated in a minute amount marine natural product from the methanol extract of the blue sponge Reniera sp. inhabiting a small marine lake in Urukhapel Island, Palau. See:. He H., and Faulkner D.J. J. Org. Chem. 54 (1989) 5822-5824
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(1989)
J. Org. Chem.
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, pp. 5822-5824
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He, H.1
Faulkner, D.J.2
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10
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66549120989
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note
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5 (5, 29.5 mg).
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11
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66549098199
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note
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3); CD (c 0.016 mmol/L, MeOH, 24 °C) -3.91 (346), 0 (290), +6.41 (264), +0.47 (234), +0.77 (229), +0.60 (224), +4.99 (214).
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12
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0023737218
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Kubo A., Saito N., Yamato H., Masubuchi K., and Nakamura M. J. Org. Chem. 53 (1988) 4295-4310
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(1988)
J. Org. Chem.
, vol.53
, pp. 4295-4310
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Kubo, A.1
Saito, N.2
Yamato, H.3
Masubuchi, K.4
Nakamura, M.5
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13
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0023157711
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Kubo A., Saito N., Kitahara Y., Takahashi K., Yazawa K., and Arai T. Chem. Pharm. Bull. 35 (1987) 440-442
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(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 440-442
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Kubo, A.1
Saito, N.2
Kitahara, Y.3
Takahashi, K.4
Yazawa, K.5
Arai, T.6
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15
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66549104412
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note
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3); CD (c 0.016 mmol/L, MeOH, 24 °C) -2.73 (356), -1.06 (301), -1.36 (292), 0 (285), +6.56 (264), 0 (239), -4.55 (223), 0 (216), +7.10 (211).
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16
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66549126384
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note
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3); CD (c 0.034 mmol/L, MeOH, 24 °C) -1.74 (343), 0 (270), +0.43 (261), +0.15 (246), +6.87 (212).
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17
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66549095529
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note
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50 was expressed as the concentration at which cell growth was inhibited by 50% compared with the untreated control.
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22
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33646188855
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Ceballos P.A., Pérez M., Cuevas C., Francesch A., Manzanares I., and Echavarren A.M. Eur. J. Org. Chem. (2006) 1926-1933
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(2006)
Eur. J. Org. Chem.
, pp. 1926-1933
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Ceballos, P.A.1
Pérez, M.2
Cuevas, C.3
Francesch, A.4
Manzanares, I.5
Echavarren, A.M.6
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