Draft:Meluadrine

Meluadrine
Clinical data
Other names	HSR-81; (R)-4-Hydroxytulobuterol
Drug class	Sympathomimetic; Tocolytic; β2-Adrenergic receptor agonist
Identifiers
	IUPAC name 4-[(1R)-2-(tert-butylamino)-1-hydroxyethyl]-3-chlorophenol;
CAS Number	134865-33-1 ; 134865-37-5 (tartrate);
PubChem CID	3045414;
ChemSpider	142963;
UNII	FYC8314117;
ChEMBL	ChEMBL2104709;
Chemical and physical data
Formula	C12H18ClNO2
Molar mass	243.73 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CC(C)(C)NC[C@@H](C1=C(C=C(C=C1)O)Cl)O;
	InChI InChI=1S/C12H18ClNO2/c1-12(2,3)14-7-11(16)9-5-4-8(15)6-10(9)13/h4-6,11,14-16H,7H2,1-3H3/t11-/m0/s1; Key:LIXBJWRFCNRAPA-NSHDSACASA-N;

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Instructions · What links here · Meluadrine (talk: + · bio) · (log) · Copyvios report · reFill · Citation Bot · (Search: Google, Wikipedia) · Submitted 8 hours ago by 75.46.150.155 (talk: D · +) · Last edited 5 hours ago by Jlwoodwa

Meluadrine (INNTooltip International Nonproprietary Name), also known as meluadrine tartrate (JANTooltip Japanese Accepted Name; developmental code name HSR-81) in the case of the tartrate salt, is a sympathomimetic and β₂-adrenergic receptor agonist which was studied as a tocolytic drug but was never marketed.^[1]^[2]^[3]^[4]^[5] It was first described in the literature by 1994.^[6] The drug is also known as (R)-4-hydroxytulobuterol and is an active metabolite of tulobuterol.^[7]

References

^ Ballard A, Narduolo S, Ahmad HO, Cosgrove DA, Leach AG, Buurma NJ (June 2019). "The problem of racemization in drug discovery and tools to predict it". Expert Opin Drug Discov. 14 (6): 527–539. doi:10.1080/17460441.2019.1588881. PMID 30882254.
^ https://cdn.who.int/media/docs/default-source/international-nonproprietary-names-(inn)/stembook-2018.pdf#page=95
^ Matsuda Y, Kouno S, Sakamoto H, Ikenoue T (October 2002). "Effects of meluadrine tartrate and ritodrine hydrochloride on oxytocin-induced uterine contraction, uterine arterial blood flow and maternal cardiovascular function in pregnant goats". Jpn J Pharmacol. 90 (2): 107–13. doi:10.1254/jjp.90.107. PMID 12419879.
^ Matsuda Y, Kouno S, Sakamoto H, Ikenoue T (October 2002). "Effects of meluadrine tartrate on maternal metabolic responses and fetal hemodynamics in pregnant goats". Jpn J Pharmacol. 90 (2): 114–120. doi:10.1254/jjp.90.114. PMID 12419880.
^ Ohashi T, Hashimoto S, Morikawa K, Kato H, Ito Y, Asano M, Azuma H (July 1996). "Potent inhibition of spontaneous rhythmic contraction by a novel beta 2-adrenoceptor agonist, HSR-81, in pregnant rat uterus". Eur J Pharmacol. 307 (3): 315–322. doi:10.1016/0014-2999(96)00277-4. PMID 8836620.
^ Hashimoto, S. (1994). Inhibitory effect of HSR-81, a novel β2-adrenoceptor agonist, on uterine contraction in late pregnancy. Jpn J Pharmacol, 64, 211. https://scholar.google.com/scholar?cluster=13515647726305291847
^ Glushkova, M. A.; Popkov, S. V.; Burdeinyi, M. L. (2020). "Synthesis of the β2-Agonist Tulobuterol and Its Metabolite 4-Hydroxytulobuterol". Russian Journal of Organic Chemistry. 56 (3). Pleiades Publishing Ltd: 390–394. doi:10.1134/s1070428020030045. ISSN 1070-4280.

This drug article relating to the cardiovascular system is a stub. You can help Wikipedia by expanding it.

[BallardNarduoloAhmad2019-1] Ballard A, Narduolo S, Ahmad HO, Cosgrove DA, Leach AG, Buurma NJ (June 2019). "The problem of racemization in drug discovery and tools to predict it". Expert Opin Drug Discov. 14 (6): 527–539. doi:10.1080/17460441.2019.1588881. PMID 30882254.

[WHO-INN-2018-2] ttps://cdn.who.int/media/docs/default-source/international-nonproprietary-names-(inn)/stembook-2018.pdf#page=95

[MatsudaKounoSakamoto2002a-3] Matsuda Y, Kouno S, Sakamoto H, Ikenoue T (October 2002). "Effects of meluadrine tartrate and ritodrine hydrochloride on oxytocin-induced uterine contraction, uterine arterial blood flow and maternal cardiovascular function in pregnant goats". Jpn J Pharmacol. 90 (2): 107–13. doi:10.1254/jjp.90.107. PMID 12419879.

[MatsudaKounoSakamoto2002b-4] Matsuda Y, Kouno S, Sakamoto H, Ikenoue T (October 2002). "Effects of meluadrine tartrate on maternal metabolic responses and fetal hemodynamics in pregnant goats". Jpn J Pharmacol. 90 (2): 114–120. doi:10.1254/jjp.90.114. PMID 12419880.

[OhashiHashimotoMorikawa1996-5] Ohashi T, Hashimoto S, Morikawa K, Kato H, Ito Y, Asano M, Azuma H (July 1996). "Potent inhibition of spontaneous rhythmic contraction by a novel beta 2-adrenoceptor agonist, HSR-81, in pregnant rat uterus". Eur J Pharmacol. 307 (3): 315–322. doi:10.1016/0014-2999(96)00277-4. PMID 8836620.

[Hashimoto1994-6] Hashimoto, S. (1994). Inhibitory effect of HSR-81, a novel β2-adrenoceptor agonist, on uterine contraction in late pregnancy. Jpn J Pharmacol, 64, 211. https://scholar.google.com/scholar?cluster=13515647726305291847

[GlushkovaPopkovBurdeinyi2020-7] Glushkova, M. A.; Popkov, S. V.; Burdeinyi, M. L. (2020). "Synthesis of the β2-Agonist Tulobuterol and Its Metabolite 4-Hydroxytulobuterol". Russian Journal of Organic Chemistry. 56 (3). Pleiades Publishing Ltd: 390–394. doi:10.1134/s1070428020030045. ISSN 1070-4280.

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Phenethylamines	Psychedelics: 25B-NBOMe 25C-NBOMe 25D-NBOMe 25I-NBOMe 25N-NBOMe 2C-B 2C-B-AN 2C-Bn 2C-Bu 2C-C 2C-CN 2C-CP 2C-D 2C-E 2C-EF 2C-F 2C-G 2C-G-1 2C-G-2 2C-G-3 2C-G-4 2C-G-5 2C-G-6 2C-G-N 2C-H 2C-I 2C-iP 2C-N 2C-NH2 2C-O 2C-O-4 2C-P 2C-Ph 2C-SE 2C-T 2C-T-2 2C-T-3 2C-T-4 2C-T-5 2C-T-6 2C-T-7 2C-T-8 2C-T-9 2C-T-10 2C-T-11 2C-T-12 2C-T-13 2C-T-14 2C-T-15 2C-T-16 2C-T-17 2C-T-18 2C-T-19 2C-T-20 2C-T-21 2C-T-22 2C-T-22.5 2C-T-23 2C-T-24 2C-T-25 2C-T-27 2C-T-28 2C-T-30 2C-T-31 2C-T-32 2C-T-33 2C-TFE 2C-TFM 2C-YN 2C-V Allylescaline DESOXY Escaline Isoproscaline Jimscaline Macromerine MEPEA Mescaline Metaescaline Methallylescaline Proscaline Psi-2C-T-4 TCB-2 Stimulants: Phenylethanolamine Hordenine Phenethylamine Phenpromethamine α-Methylphenethylamine (amphetamine) β-Methylphenethylamine m-Methylphenethylamine N-Methylphenethylamine o-Methylphenethylamine p-Methylphenethylamine Methylphenidate Entactogens: Lophophine MDPEA MDMPEA Others: BOH DMPEA
Amphetamines	Psychedelics: 3C-AL 3C-BZ 3C-E 3C-MAL 3C-P Aleph Beatrice Bromo-DragonFLY D-Deprenyl DMA DMCPA DMMDA DOB DOC DOEF DOET DOI DOM DON DOPR DOTFM Ganesha MMDA MMDA-2 Psi-DOM TMA TeMA ZDCM-04 Stimulants: 2-FA 2-FMA 3-FA 3-FMA Acridorex Alfetamine Amfecloral Amfepentorex Amphetamine (Dextroamphetamine, Levoamphetamine) Amphetaminil Benfluorex Benzphetamine Cathine Clobenzorex Dimethylamphetamine Ephedrine Etilamfetamine Fencamfamin Fencamine Fenethylline Fenfluramine (Dexfenfluramine, Levofenfluramine) Fenproporex Flucetorex Fludorex Formetorex Furfenorex Gepefrine 4-Hydroxyamphetamine Iofetamine Isopropylamphetamine Lefetamine Lisdexamfetamine Mefenorex Metaraminol Methamphetamine (Dextromethamphetamine, Levomethamphetamine) Methoxyphenamine MMA Morforex Norfenfluramine L-Norpseudoephedrine N,alpha-Diethylphenylethylamine Oxifentorex Oxilofrine Ortetamine PBA PCA PFA PFMA PIA PMA PMEA PMMA Phenylpropanolamine Pholedrine Prenylamine Propylamphetamine Pseudoephedrine Sibutramine Tiflorex Tranylcypromine Xylopropamine Zylofuramine Entactogens: 4-FA 4-FMA 4-MA 4-MMA 4-MTA 5-APB 5-APDB 5-EAPB 5-IT 5-MAPB 5-MAPDB 6-APB 6-APDB 6-Chloro-MDMA 6-EAPB 6-IT 6-MAPB 6-MAPDB EDA IAP 2,3-MDA 3,4-MDA (tenamfetamine) MDEA MDHMA MDMA (midomafetamine) MDOH Methamnetamine MMDMA Naphthylaminopropane TAP Others: 3,4-DCA Amiflamine DiFMDA Selegiline (also D-Deprenyl)
Phentermines	Stimulants: Chlorphentermine Cloforex Clortermine Etolorex Mephentermine Pentorex Phentermine Entactogens: MDPH MDMPH Others: Cericlamine
Cathinones	Stimulants: 3-FMC 4-MC 4-BMC 4-CMC 4-EMC 4-FMC 4-MEC 4-MeMABP 4-MPD Amfepramone Benzedrone Brephedrone Buphedrone Bupropion Cathinone Dimethylcathinone Ethcathinone Eutylone Hydroxybupropion Methcathinone Methedrone NEB N-Ethylhexedrone N-Ethylpentedrone Pentedrone Pentylone Radafaxine Entactogens: 3,4-DMMC 3-MMC Butylone Ethylone Methylone Methylenedioxycathinone Mephedrone
Phenylisobutylamines	Entactogens: 4-CAB 4-MAB Ariadne BDB Butylone EBDB Eutylone MBDB Stimulants: Phenylisobutylamine
Phenylalkylpyrrolidines	Stimulants: α-PBP α-PHP α-PPP α-PVP MDPBP MDPPP MDPV 4-MePBP 4-MePHP 4-MePPP MOPPP MOPVP MPBP MPHP MPPP Naphyrone PEP Prolintane Pyrovalerone
Catecholamines (and close relatives)	6-FNE 6-OHDA a-Me-DA a-Me-TRA Adrenochrome Ciladopa D-DOPA (Dextrodopa) Dimetofrine Dopamine Epinephrine Epinine Etilefrine Ethylnorepinephrine Fenclonine Ibopamine Isoprenaline Isoetarine L-DOPA (Levodopa) L-DOPS (Droxidopa) L-Phenylalanine L-Tyrosine m-Tyramine Metanephrine Metaraminol Metaterol Metirosine Methyldopa N,N-Dimethyldopamine Nordefrin (Levonordefrin) Norepinephrine Norfenefrine (m-Octopamine) Normetanephrine Orciprenaline p-Octopamine p-Tyramine Phenylephrine Synephrine
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