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24:
372:
580:
109:
573:
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250:
InChI=1S/C20H26N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h4-6,8,11,13-14,19-20,23H,3,7,9-10,12H2,1-2H3/t13-,14-,19-,20+/m0/s1
260:
InChI=1/C20H26N2O2/c1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18/h4-6,8,11,13-14,19-20,23H,3,7,9-10,12H2,1-2H3/t13-,14-,19-,20+/m0/s1
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Huffman, Aarin M.; Ayariga, Joseph A.; Napier, Audrey; Robertson, Boakai K.; Abugri, Daniel A. (2022).
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513:"Inhibition of Toxoplasma gondii Growth by Dihydroquinine and Its Mechanisms of Action"
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Except where otherwise noted, data are given for materials in their
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membrane damage, but does not disrupt host mitochondrial
851:
517:Frontiers in Cellular and Infection Microbiology
172:
77:
44:)-octan-2-yl]-(6-methoxyquinolin-4-yl)methanol
574:
284:O(C1N2CCC(C(CC)C2)C1)C3=CC=NC4=CC=C(OC)C=C43
490:
435:. A derivative of this molecule is used as
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450:DHQ also inhibits growth of the parasite
192:
56:)-10,11-Dihydro-6'-methoxycinchonan-9-ol
221:
852:
289:O(c4cc1c(nccc1(O)2N3CC(C2)(CC)C3)cc4)C
141:
562:
498:"Dihydroquinine chemical information"
253:Key: LJOQGZACKSYWCH-WZBLMQSHSA-N
263:Key: LJOQGZACKSYWCH-WZBLMQSHBC
163:
13:
14:
886:
589:Other drugs for disorders of the
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322:
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22:
366:(at 25 °C , 100 kPa).
748:Histone deacetylase inhibitors
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328:
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1:
483:
667:Delandistrogene moxeparvovec
7:
471:
10:
891:
682:Antisense oligonucleotides
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530:10.3389/fcimb.2022.852889
445:Sharpless dihydroxylation
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49:
35:
30:
21:
672:Onasemnogene abeparvovec
643:clostridium histolyticum
591:musculo-skeletal system
466:reactive oxygen species
875:Quinuclidine alkaloids
870:Quinoline alkaloids
500:. ChemIndustry.com.
423:closely related to
346: g·mol
18:
860:Secondary alcohols
837:Never to phase III
468:(ROS) generation.
462:membrane potential
393:Infobox references
16:
847:
846:
453:Toxoplasma gondii
429:specific rotation
421:cinchona alkaloid
401:Chemical compound
399:
398:
206:CompTox Dashboard
110:Interactive image
103:Interactive image
882:
772:Aceneuramic acid
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478:Dihydroquinidine
417:organic compound
407:, also known as
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305:Chemical formula
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17:Dihydroquinine
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405:Dihydroquinine
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437:chiral ligand
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797:Palovarotene
787:Chondrocytes
642:
641:Collagenase
613:Hydroquinine
612:
520:
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492:
456:by inducing
451:
449:
431:is −148° in
412:
409:hydroquinine
408:
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62:Identifiers
53:
50:Other names
41:
823:from market
733:Deflazacort
715:Viltolarsen
695:Drisapersen
636:Chymopapain
356:173–175 °C
298:Properties
148:100.007.578
854:Categories
756:Givinostat
738:Vamorolone
710:Nusinersen
705:Golodirsen
700:Eteplirsen
690:Casimersen
631:Bromelains
484:References
339:Molar mass
194:31J3Q51T6L
121:ChemSpider
90:3D model (
69:CAS Number
37:IUPAC name
833:Phase III
821:Withdrawn
802:Risdiplam
782:Branaplam
539:2235-2988
419:and as a
777:Ataluren
472:See also
415:, is an
79:522-66-7
649:Trypsin
623:Enzymes
604:Quinine
548:9131874
439:in the
433:ethanol
425:quinine
386:what is
384: (
344:326.440
161:PubChem
816:WHO-EM
545:
537:
441:AD-mix
427:. The
381:verify
378:
277:SMILES
174:121515
130:108426
31:Names
765:Other
242:InChI
92:JSmol
52:(8α,9
535:ISSN
443:for
185:UNII
595:M09
543:PMC
525:doi
413:DHQ
411:or
211:EPA
164:CID
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376:Y
332:2
329:O
326:2
323:N
317:H
311:C
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209:(
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54:R
42:R
40:(
Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.
