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InChI=1S/C41H46N4O3/c1-5-24-21-44-17-15-32-27-11-7-9-13-34(27)45-39(40(46)47-4)29(24)20-37(44)41(32,45)16-14-25-22-48-23-31-28(25)18-36-38-30(19-35(31)42(36)2)26-10-6-8-12-33(26)43(38)3/h5-14,16,22,28-29,31-32,35-37,39H,15,17-21,23H2,1-4H3/b16-14+,24-5-/t28-,29-,31+,32+,35-,36-,37-,39-,41-/m0/s1
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Keawpradub, N.; Kirby, G. C.; Steele, J. C.; Houghton, P. J. (1999). "Antiplasmodial activity of extracts and alkaloids of three
Alstonia species from Thailand".
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64:)-17-icosa-2(10),4,6,8,16-pentaen-17-yl]ethenyl]-13-ethylidene-1,11-diazapentacyclooctadeca-2,4,6-triene-18-carboxylate
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C/C=C\1/CN2CC3C4=CC=CC=C4N53(2C15C(=O)OC)/C=C/C6=COC76C8C9=C(C7N8C)C1=CC=CC=C1N9C
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Except where otherwise noted, data are given for materials in their
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313:alkaloid with antiplasmodial activity.
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201:Key: NOKYQXVIWFQLED-HXCLOJFDSA-N
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289:(at 25 °C , 100 kPa).
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344:10.1055/s-1999-14043
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301:Chemical compound
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17:Macrocarpamine
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338:(8): 690–694.
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98:3D model (
87:66408-46-6
77:CAS Number
37:IUPAC name
40:Methyl (8
366:Category
352:10630106
310:Alstonia
151:28496174
277:642.844
176:5472477
163:PubChem
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307:is an
215:SMILES
122:ChEMBL
31:Names
190:InChI
100:JSmol
348:PMID
340:doi
166:CID
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262:O
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256:N
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62:S
58:S
54:S
50:S
46:E
42:R
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