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ZK-93423

ZK-93423 is an anxiolytic drug from the β-Carboline family, closely related to abecarnil.[1] It is a nonbenzodiazepine GABAA agonist which is not subtype selective and stimulates α1, α2, α3, and α5-subunit containing GABAA receptors equally.[2] It has anticonvulsant, muscle relaxant and appetite stimulating properties comparable to benzodiazepine drugs.[3][4][5][6] ZK-93423 has also been used as a base to develop new and improved beta-carboline derivatives and help map the binding site of the GABAA receptor.[7][8][9][10][11][12]

ZK-93423
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: legal
Identifiers
  • ethyl 4-(methoxymethyl)-6-(phenylmethoxy) -9H-pyrido[5,4-b]indole-3-carboxylate
CAS Number
  • 83910-44-5 Y
PubChem CID
  • 121926
IUPHAR/BPS
  • 4346
ChemSpider
  • 108771
UNII
  • B6PWX5B47Q
ChEBI
  • CHEBI:92593
ChEMBL
  • ChEMBL1518572
CompTox Dashboard (EPA)
  • DTXSID101004052
Chemical and physical data
FormulaC23H22N2O4
Molar mass390.439 g·mol−1
3D model (JSmol)
  • Interactive image
  • c3ccccc3COc(cc4)cc2c4[nH]c(cnc1C(=O)OCC)c2c1COC
  • InChI=1S/C23H22N2O4/c1-3-28-23(26)22-18(14-27-2)21-17-11-16(29-13-15-7-5-4-6-8-15)9-10-19(17)25-20(21)12-24-22/h4-12,25H,3,13-14H2,1-2H3
  • Key:ALBKMJDFBZVHAK-UHFFFAOYSA-N
 NY (what is this?)  (verify)

See also edit

References edit

  1. ^ Zhang H, Larock RC (December 2002). "Synthesis of beta- and gamma-carbolines by the palladium-catalyzed iminoannulation of alkynes". The Journal of Organic Chemistry. 67 (26): 9318–30. doi:10.1021/jo026317u. PMID 12492334.
  2. ^ Stephens DN, Shearman GT, Kehr W (1984). "Discriminative stimulus properties of beta-carbolines characterized as agonists and inverse agonists at central benzodiazepine receptors". Psychopharmacology. 83 (3): 233–9. doi:10.1007/BF00464787. PMID 6089245. S2CID 1479932.
  3. ^ Klockgether T, Pardowitz I, Schwarz M, Sontag KH, Turski L (October 1985). "Evaluation of the muscle relaxant properties of a novel beta-carboline, ZK 93423 in rats and cats". British Journal of Pharmacology. 86 (2): 357–66. doi:10.1111/j.1476-5381.1985.tb08904.x. PMC 1916712. PMID 3931731.
  4. ^ Cooper SJ (January 1986). "Hyperphagic and anorectic effects of beta-carbolines in a palatable food consumption test: comparisons with triazolam and quazepam". European Journal of Pharmacology. 120 (3): 257–65. doi:10.1016/0014-2999(86)90466-8. PMID 3753939.
  5. ^ File SE, Baldwin HA (September 1987). "Effects of beta-carbolines in animal models of anxiety". Brain Research Bulletin. 19 (3): 293–9. doi:10.1016/0361-9230(87)90097-9. PMID 3315125. S2CID 54428766.
  6. ^ Löscher W, Hönack D, Hashem A (November 1987). "Anticonvulsant efficacy of clonazepam and the beta-carboline ZK 93423 during chronic treatment in amygdala-kindled rats". European Journal of Pharmacology. 143 (3): 403–14. doi:10.1016/0014-2999(87)90464-X. PMID 3691663.
  7. ^ Dodd RH, Ouannès C, Potier MC, Prado de Carvalho L, Rossier J, Potier P (July 1987). "Synthesis of beta-carboline-benzodiazepine hybrid molecules: use of the known structural requirements for benzodiazepine and beta-carboline binding in designing a novel, high-affinity ligand for the benzodiazepine receptor". Journal of Medicinal Chemistry. 30 (7): 1248–54. doi:10.1021/jm00390a023. PMID 3037081.
  8. ^ Hollinshead SP, Trudell ML, Skolnick P, Cook JM (March 1990). "Structural requirements for agonist actions at the benzodiazepine receptor: studies with analogues of 6-(benzyloxy)-4-(methoxymethyl)-beta-carboline-3-carboxylic acid ethyl ester". Journal of Medicinal Chemistry. 33 (3): 1062–9. doi:10.1021/jm00165a028. PMID 1968513.
  9. ^ Diaz-Arauzo H, Evoniuk GE, Skolnick P, Cook JM (May 1991). "The agonist pharmacophore of the benzodiazepine receptor. Synthesis of a selective anticonvulsant/anxiolytic". Journal of Medicinal Chemistry. 34 (5): 1754–6. doi:10.1021/jm00109a035. PMID 1674542.
  10. ^ Sharma RC, Ojha TN, Tiwari S, Singh P (1992). "Quantitative structure-activity relationship study of some benzodiazepine-receptor ligands having inverse agonist/antagonist and agonist actions". Drug Design and Discovery. 9 (2): 135–43. PMID 1338366.
  11. ^ Cox ED, Diaz-Arauzo H, Huang Q, Reddy MS, Ma C, Harris B, McKernan R, Skolnick P, Cook JM (July 1998). "Synthesis and evaluation of analogues of the partial agonist 6-(propyloxy)-4-(methoxymethyl)-beta-carboline-3-carboxylic acid ethyl ester (6-PBC) and the full agonist 6-(benzyloxy)-4-(methoxymethyl)-beta-carboline-3-carboxylic acid ethyl ester (Zk 93423) at wild type and recombinant GABAA receptors". Journal of Medicinal Chemistry. 41 (14): 2537–52. doi:10.1021/jm970460b. PMID 9651158.
  12. ^ Ferretti V, Gilli P, Borea PA (August 2004). "Structural features controlling the binding of beta-carbolines to the benzodiazepine receptor". Acta Crystallographica B. 60 (Pt 4): 481–9. doi:10.1107/S0108768104013564. PMID 15258407.

93423, anxiolytic, drug, from, carboline, family, closely, related, abecarnil, nonbenzodiazepine, gabaa, agonist, which, subtype, selective, stimulates, subunit, containing, gabaa, receptors, equally, anticonvulsant, muscle, relaxant, appetite, stimulating, pr. ZK 93423 is an anxiolytic drug from the b Carboline family closely related to abecarnil 1 It is a nonbenzodiazepine GABAA agonist which is not subtype selective and stimulates a1 a2 a3 and a5 subunit containing GABAA receptors equally 2 It has anticonvulsant muscle relaxant and appetite stimulating properties comparable to benzodiazepine drugs 3 4 5 6 ZK 93423 has also been used as a base to develop new and improved beta carboline derivatives and help map the binding site of the GABAA receptor 7 8 9 10 11 12 ZK 93423Clinical dataATC codenoneLegal statusLegal statusIn general legalIdentifiersIUPAC name ethyl 4 methoxymethyl 6 phenylmethoxy 9H pyrido 5 4 b indole 3 carboxylateCAS Number83910 44 5 YPubChem CID121926IUPHAR BPS4346ChemSpider108771UNIIB6PWX5B47QChEBICHEBI 92593ChEMBLChEMBL1518572CompTox Dashboard EPA DTXSID101004052Chemical and physical dataFormulaC 23H 22N 2O 4Molar mass390 439 g mol 13D model JSmol Interactive imageSMILES c3ccccc3COc cc4 cc2c4 nH c cnc1C O OCC c2c1COCInChI InChI 1S C23H22N2O4 c1 3 28 23 26 22 18 14 27 2 21 17 11 16 29 13 15 7 5 4 6 8 15 9 10 19 17 25 20 21 12 24 22 h4 12 25H 3 13 14H2 1 2H3Key ALBKMJDFBZVHAK UHFFFAOYSA N N Y what is this verify See also editZK 93426References edit Zhang H Larock RC December 2002 Synthesis of beta and gamma carbolines by the palladium catalyzed iminoannulation of alkynes The Journal of Organic Chemistry 67 26 9318 30 doi 10 1021 jo026317u PMID 12492334 Stephens DN Shearman GT Kehr W 1984 Discriminative stimulus properties of beta carbolines characterized as agonists and inverse agonists at central benzodiazepine receptors Psychopharmacology 83 3 233 9 doi 10 1007 BF00464787 PMID 6089245 S2CID 1479932 Klockgether T Pardowitz I Schwarz M Sontag KH Turski L October 1985 Evaluation of the muscle relaxant properties of a novel beta carboline ZK 93423 in rats and cats British Journal of Pharmacology 86 2 357 66 doi 10 1111 j 1476 5381 1985 tb08904 x PMC 1916712 PMID 3931731 Cooper SJ January 1986 Hyperphagic and anorectic effects of beta carbolines in a palatable food consumption test comparisons with triazolam and quazepam European Journal of Pharmacology 120 3 257 65 doi 10 1016 0014 2999 86 90466 8 PMID 3753939 File SE Baldwin HA September 1987 Effects of beta carbolines in animal models of anxiety Brain Research Bulletin 19 3 293 9 doi 10 1016 0361 9230 87 90097 9 PMID 3315125 S2CID 54428766 Loscher W Honack D Hashem A November 1987 Anticonvulsant efficacy of clonazepam and the beta carboline ZK 93423 during chronic treatment in amygdala kindled rats European Journal of Pharmacology 143 3 403 14 doi 10 1016 0014 2999 87 90464 X PMID 3691663 Dodd RH Ouannes C Potier MC Prado de Carvalho L Rossier J Potier P July 1987 Synthesis of beta carboline benzodiazepine hybrid molecules use of the known structural requirements for benzodiazepine and beta carboline binding in designing a novel high affinity ligand for the benzodiazepine receptor Journal of Medicinal Chemistry 30 7 1248 54 doi 10 1021 jm00390a023 PMID 3037081 Hollinshead SP Trudell ML Skolnick P Cook JM March 1990 Structural requirements for agonist actions at the benzodiazepine receptor studies with analogues of 6 benzyloxy 4 methoxymethyl beta carboline 3 carboxylic acid ethyl ester Journal of Medicinal Chemistry 33 3 1062 9 doi 10 1021 jm00165a028 PMID 1968513 Diaz Arauzo H Evoniuk GE Skolnick P Cook JM May 1991 The agonist pharmacophore of the benzodiazepine receptor Synthesis of a selective anticonvulsant anxiolytic Journal of Medicinal Chemistry 34 5 1754 6 doi 10 1021 jm00109a035 PMID 1674542 Sharma RC Ojha TN Tiwari S Singh P 1992 Quantitative structure activity relationship study of some benzodiazepine receptor ligands having inverse agonist antagonist and agonist actions Drug Design and Discovery 9 2 135 43 PMID 1338366 Cox ED Diaz Arauzo H Huang Q Reddy MS Ma C Harris B McKernan R Skolnick P Cook JM July 1998 Synthesis and evaluation of analogues of the partial agonist 6 propyloxy 4 methoxymethyl beta carboline 3 carboxylic acid ethyl ester 6 PBC and the full agonist 6 benzyloxy 4 methoxymethyl beta carboline 3 carboxylic acid ethyl ester Zk 93423 at wild type and recombinant GABAA receptors Journal of Medicinal Chemistry 41 14 2537 52 doi 10 1021 jm970460b PMID 9651158 Ferretti V Gilli P Borea PA August 2004 Structural features controlling the binding of beta carbolines to the benzodiazepine receptor Acta Crystallographica B 60 Pt 4 481 9 doi 10 1107 S0108768104013564 PMID 15258407 Retrieved from https en wikipedia org w index php title ZK 93423 amp oldid 1135429267, wikipedia, wiki, book, books, library,

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