Ketcher 04051816592D 1 1.00000 0.00000 0 30 32 0 1 0 999 V2000 14.2328 -7.9271 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.0974 -7.4292 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.0974 -6.4281 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 14.2328 -5.9251 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 13.3680 -7.4292 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 13.3710 -6.4304 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.5083 -5.9328 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6418 -6.4279 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6436 -7.4306 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.5071 -7.9285 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.9620 -5.9351 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.8286 -6.4377 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.6921 -5.9431 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 17.6955 -4.9409 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 16.8283 -4.4354 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 15.9633 -4.9381 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 18.5639 -4.4392 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 14.2328 -8.9282 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.5083 -8.9296 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 12.5102 -4.9318 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6436 -4.4271 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.7738 -4.9227 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 11.6536 -3.4285 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.7871 -2.9237 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 12.5234 -2.9329 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.9116 -4.4153 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0417 -4.9109 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 8.1751 -4.4061 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 9.0341 -5.9137 0.0000 C 0 0 0 0 0 0 0 0 0 0 0 0 10.7755 -5.9262 0.0000 O 0 0 0 0 0 0 0 0 0 0 0 0 6 4 1 0 0 0 5 1 1 0 0 0 1 2 1 0 0 0 2 3 1 0 0 0 3 4 1 0 0 0 5 6 2 0 0 0 6 7 1 0 0 0 7 8 2 0 0 0 8 9 1 0 0 0 9 10 2 0 0 0 10 5 1 0 0 0 11 12 2 0 0 0 12 13 1 0 0 0 13 14 2 0 0 0 14 15 1 0 0 0 15 16 2 0 0 0 16 11 1 0 0 0 3 11 1 6 0 0 14 17 1 0 0 0 1 18 2 0 0 0 10 19 1 0 0 0 7 20 1 0 0 0 20 21 1 0 0 0 21 22 1 1 0 0 21 23 1 0 0 0 23 24 2 0 0 0 23 25 1 0 0 0 22 26 1 0 0 0 26 27 1 0 0 0 27 28 2 0 0 0 27 29 1 0 0 0 8 30 1 0 0 0 M END > CHEBI:66297 > remangiflavanone A > A trihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at positions 5, 7 and 4' and a lavandulyl group at position 8. Isolated from Physena madagascariensis, it exhibits antibacterial activity. > 3 > 5,7,4'-trihydroxy-8-(2-isopropyl-5-methyl-5-hexenyl)flavanone; 5,7,2',4'-tetrahydroxy-8-(2-isopropyl-5-methyl-5-hexenyl)flavanone; (2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R)-5-methyl-2-(1-methylethenyl)-5-hexen-1-yl]-2,3-dihydro-4H-1-benzopyran-4-one; (2S)-5,7,4'-trihydroxy-8-lavandulylflavanone > (2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-5-en-1-yl]-2,3-dihydro-4H-chromen-4-one > C25H28O5 > 408.488 > 408.19367 > 0 > C1(C2=C(O[C@@H](C1)C3=CC=C(C=C3)O)C(=C(C=C2O)O)C[C@@H](CCC(=C)C)C(=C)C)=O > InChI=1S/C25H28O5/c1-14(2)5-6-17(15(3)4)11-19-20(27)12-21(28)24-22(29)13-23(30-25(19)24)16-7-9-18(26)10-8-16/h7-10,12,17,23,26-28H,1,3,5-6,11,13H2,2,4H3/t17-,23+/m1/s1 > NPTHXJUVZWZDJB-HXOBKFHXSA-N > 8658227 > LMPK12140299 > 10978202 $$$$