Dihydrexidine
{{Short description|Chemical compound}}
{{Drugbox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 414782444
| IUPAC_name = 5,6,6a,7,8,12b-hexahydro-benzo(a)phenanthridine-10,11-diol
| image = Dihydrexidine structure.png
| tradename =
| pregnancy_category =
| legal_status =
| routes_of_administration =
| bioavailability =
| metabolism =
| elimination_half-life =
| excretion =
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 123039-93-0
| ATC_prefix = none
| ATC_suffix =
| PubChem = 5311070
| UNII_Ref = {{fdacite|changed|FDA}}
| UNII = 32D64VH037
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 25856
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 5036130
| C=17 | H=17 | N=1 | O=2
| smiles = c1ccc2c(c1)CN[C@H]3[C@H]2c4cc(c(cc4CC3)O)O
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 1S/C17H17NO2/c19-15-7-10-5-6-14-17(13(10)8-16(15)20)12-4-2-1-3-11(12)9-18-14/h1-4,7-8,14,17-20H,5-6,9H2/t14-,17-/m1/s1
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = BGOQGUHWXBGXJW-RHSMWYFYSA-N
}}
Dihydrexidine (DAR-0100) is a moderately selective full agonist at the dopamine D1 and D5 receptors.{{cite journal | vauthors = Lovenberg TW, Brewster WK, Mottola DM, Lee RC, Riggs RM, Nichols DE, Lewis MH, Mailman RB | title = Dihydrexidine, a novel selective high potency full dopamine D-1 receptor agonist. | journal = Eur J Pharmacol | volume = 166 | issue = 1 | pages = 111–113 | year = 1989 | pmid = 2572425 | doi=10.1016/0014-2999(89)90690-0}} It has approximately 10-fold selectivity for D1 and D5 over the D2 receptor.{{cite journal | vauthors = Mottola DM, Brewster WK, Cook LL, Nichols DE, Mailman RB | title = Dihydrexidine, a novel full efficacy D1 dopamine receptor agonist. | journal = J Pharmacol Exp Ther | volume = 262 | issue = 1 | pages = 383–393 | year = 1992 | pmid = 1352553 }} Although dihydrexidine has some affinity for the D2 receptor, it has functionally selective (highly biased) D2 signaling,{{Cite journal | last1 = Kilts | first1 = JD.| title = Functional selectivity of dopamine receptor agonists. II. Actions of dihydrexidine in D2L receptor-transfected MN9D cells and pituitary lactotrophs. | journal = J Pharmacol Exp Ther | volume = 301 | issue = 3 | pages = 1179–89 | year = 2002 | doi = 10.1124/jpet.301.3.1179| pmid = 12023553 |display-authors=etal}} thereby explaining why it lacks D2 agonist behavioral qualities.{{cite journal | vauthors = ((Darney KJ Jr)), Lewis MH, Brewster WK, Nichols DE, Mailman RB | title = Behavioral effects in the rat of dihydrexidine, a high-potency, full-efficacy D1 dopamine receptor agonist. | journal = Neuropsychopharmacology | volume = 5 | issue = 3 | pages = 187–195 | year = 1991 | pmid = 1684499 }}
Dihydrexidine has shown impressive antiparkinson effects in the MPTP-primate model,{{cite journal | vauthors = Taylor JR, Lawrence MS, ((Redmond DE Jr)), Elsworth JD, Roth RH, Nichols DE, Mailman RB | title = Dihydrexidine, a full dopamine D1 agonist, reduces MPTP-induced parkinsonism in monkeys. | journal = Eur J Pharmacol | volume = 199 | issue = 3 | pages = 389–391 | year = 1991 | pmid = 1680717 | doi=10.1016/0014-2999(91)90508-N| doi-access = free }} and has been investigated for the treatment of Parkinson's disease.{{cite journal | vauthors = Mailman RB, Nichols DE | title = Dopamine D1 receptor agonists as antiparkinson drugs. | journal = Trends Pharmacol. Sci. | volume = 19 | issue = 7 | pages = 255–256 | year = 1998 | pmid = 9703756 | doi=10.1016/S0165-6147(98)01219-X}} In an early clinical trial the drug was given intravenously and led to profound hypotension so development was halted.{{cite journal | vauthors = Blanchet PJ, Fang J, Gillespie M, Sabounjian L, Locke KW, Gammans R, Mouradian MM, Chase TN | title = Effects of the full dopamine D1 receptor agonist dihydrexidine in Parkinson's disease. | journal = Clin. Neuropharmacol. | volume = 21 | issue = 6 | pages = 339–343 | year = 1998 | pmid = 9844789 }} The drug was resurrected when it was shown that smaller subcutaneous doses were safe.{{cite journal | vauthors = George MS, Molnar CE, Grenesko EL, Anderson B, Mu Q, Johnson K, Nahas Z, Knable M, Fernandes P, Juncos J, Huang X, Nichols DE, Mailman RB | title = A single 20 mg dose of dihydrexidine (DAR-0100), a full dopamine D1 agonist, is safe and tolerated in patients with schizophrenia. | journal = Schizophr. Res. | volume = 93 | issue = 1–3 | pages = 42–50 | year = 2007 | pmid = 17467956 | doi=10.1016/j.schres.2007.03.011| s2cid = 31375175 }} This led to a pilot study in schizophrenia{{cite journal | vauthors = Mu Q, Johnson K, Morgan PS, Grenesko EL, Molnar CE, Anderson B, Nahas Z, Kozel FA, Kose S, Knable M, Fernandes P, Nichols DE, Mailman RB, George MS | title = A single 20 mg dose of the full D1 dopamine agonist dihydrexidine (DAR-0100) increases prefrontal perfusion in schizophrenia. | journal = Schizophr. Res. | volume = 94 | issue = 1–3 | pages = 332–341 | year = 2007 | pmid = 17596915 | doi=10.1016/j.schres.2007.03.033| s2cid = 25497605 }} and current clinical trials to assess its efficacy in improving the cognitive and working memory deficits in schizophrenia and schizotypal disorder.
There have been several reviews of relevance to the compound.{{cite journal | vauthors = Mailman R, Huang X, Nichols DE | title = Parkinson's disease and D1 dopamine receptors. | journal = Current Opinion in Investigational Drugs | volume = 2 | issue = 11 | pages = 1582–1591 | year = 2001 | pmid = 11763161 }}{{cite journal | vauthors = Salmi P, Isacson R, Kull B | title = Dihydrexidine--the first full dopamine D1 receptor agonist. | journal = CNS Drug Rev. | volume = 10 | issue = 3 | pages = 230–242 | year = 2004 | pmid = 15492773 | doi=10.1111/j.1527-3458.2004.tb00024.x| pmc = 6741759 }}{{cite journal | vauthors = Zhang J, Xiong B, Zhen X, Zhang A | title = Dopamine D1 receptor ligands: where are we now and where are we going. | journal = Med Res Rev | volume = 29 | issue = 2 | pages = 272–294 | year = 2009 | pmid = 18642350 | doi = 10.1002/med.20130 | s2cid = 25334596 }}
References
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{{Dopamine receptor modulators}}
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