Nalfurafine: Difference between revisions
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{{Drugbox | {{Drugbox | ||
| IUPAC_name | | Verifiedfields = changed | ||
| image | | Watchedfields = changed | ||
| verifiedrevid = 447928192 | |||
| | | IUPAC_name = (2''E'')-''N''-[(5α,6β)-17-(cyclopropylmethyl)- 3,14-dihydroxy- 4,5-epoxymorphinan- 6-yl]- 3-(3-furyl)- ''N''-methylacrylamide | ||
| | | image = Nalfurafine.png | ||
<!--Clinical data--> | |||
| tradename = | |||
| Drugs.com = {{drugs.com|international|nalfurafine}} | |||
| licence_EU = <!-- EMEA requires brand name --> | |||
| licence_US = <!-- FDA may use generic name --> | |||
| | | pregnancy_AU = <!-- A / B1 / B2 / B3 / C / D / X --> | ||
| | | pregnancy_US = <!-- A / B / C / D / X --> | ||
| pregnancy_category = | |||
| legal_AU = <!-- Unscheduled / S2 / S3 / S4 / S5 / S6 / S7 / S8 / S9 --> | |||
| legal_CA = <!-- / Schedule I, II, III, IV, V, VI, VII, VIII --> | |||
| legal_UK = <!-- GSL / P / POM / CD / Class A, B, C --> | |||
| legal_US = <!-- OTC / Rx-only / Schedule I, II, III, IV, V --> | |||
| licence_EU | | legal_status = | ||
| licence_US | |||
| pregnancy_AU | |||
| pregnancy_US | |||
| pregnancy_category= | |||
| legal_AU | |||
| legal_CA | |||
| legal_UK | |||
| legal_US | |||
| legal_status | |||
| dependency_liability = | | dependency_liability = | ||
| routes_of_administration = [[Intravenous therapy|intravenous]] | | routes_of_administration = [[Intravenous therapy|intravenous]] | ||
<!--Pharmacokinetic data--> | |||
| bioavailability = | |||
| protein_bound = | |||
| metabolism = | |||
| elimination_half-life = | |||
| excretion = | |||
<!--Identifiers--> | |||
| CAS_number_Ref = {{cascite|correct|??}} | |||
| CAS_number = 152658-17-8 | |||
| ATC_prefix = V03 | |||
| ATC_suffix = AX02 | |||
| ATC_supplemental = | |||
| PubChem = 6445230 | |||
| IUPHAR_ligand = 1651 | |||
| DrugBank_Ref = {{drugbankcite|correct|drugbank}} | |||
| DrugBank = | |||
| ChEMBL_Ref = {{ebicite|changed|EBI}} | |||
| ChEMBL = 267495 | |||
| UNII_Ref = {{fdacite|correct|FDA}} | |||
| UNII = XC41AVD567 | |||
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | |||
| ChemSpiderID = 4949003 | |||
<!--Chemical data--> | |||
| C=28 | H=32 | N=2 | O=5 | |||
| molecular_weight = 476.564 g/mol | |||
| synonyms = TRK-820 | |||
| smiles = CN([C@@H]1CC[C@]2([C@H]3CC4=C5[C@]2([C@H]1OC5=C(C=C4)O)CCN3CC6CC6)O)C(=O)/C=C/C7=COC=C7 | |||
| InChI = 1/C28H32N2O5/c1-29(23(32)7-4-18-9-13-34-16-18)20-8-10-28(33)22-14-19-5-6-21(31)25-24(19)27(28,26(20)35-25)11-12-30(22)15-17-2-3-17/h4-7,9,13,16-17,20,22,26,31,33H,2-3,8,10-12,14-15H2,1H3/b7-4+/t20-,22-,26+,27+,28-/m1/s1 | |||
| InChIKey = XGZZHZMWIXFATA-UEZBDDGYBW | |||
| StdInChI_Ref = {{stdinchicite|changed|chemspider}} | |||
| StdInChI = 1S/C28H32N2O5/c1-29(23(32)7-4-18-9-13-34-16-18)20-8-10-28(33)22-14-19-5-6-21(31)25-24(19)27(28,26(20)35-25)11-12-30(22)15-17-2-3-17/h4-7,9,13,16-17,20,22,26,31,33H,2-3,8,10-12,14-15H2,1H3/b7-4+/t20-,22-,26+,27+,28-/m1/s1 | |||
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} | |||
| StdInChIKey = XGZZHZMWIXFATA-UEZBDDGYSA-N | |||
}} | }} | ||
__NOTOC__ | |||
{{SI}} | |||
{{CMG}} | |||
==Overview== | |||
'''Nalfurafine''' ([[International Nonproprietary Name|INN]] and [[United States Adopted Name|USAN]];<ref>[http://www.ama-assn.org/ama1/pub/upload/mm/365/nalfurafine_hcl.pdf Statement on a Nonproprietary Name adopted by the USAN Council]</ref> also known as AC-820, TRK-820; trade name '''Remitch''') is a [[kappa Opioid receptor|κ-opioid receptor]] [[agonist]] marketed as a treatment for [[Uremia|uremic]] [[pruritus]] in people undergoing [[hemodialysis]].<ref>{{cite web|url=http://www.acologix.com/pipeline_ac-820.html|title=AC-820|publisher=Acologix|year=2009}}</ref> | |||
{{as of|2010|1}}, it is also being investigated for the treatment of pruritus in patients with [[chronic liver disease]].<ref>{{ClinicalTrialsGov|NCT00638495|Phase II Study of TRK-820 Soft Capsules — Intractable Pruritus in Patients With Chronic Liver Disease}}</ref> | |||
==References== | |||
{{Reflist|2}} | |||
[[Category: | [[Category:Morphinans]] | ||
[[Category: | [[Category:Phenols]] | ||
[[Category:Alcohols]] | |||
[[Category:Amides]] | |||
[[Category:Semisynthetic opioids]] | |||
[[Category:Alkenes]] | |||
[[Category:Furans]] | |||
[[Category:Drug]] |
Latest revision as of 17:01, 13 April 2015
Clinical data | |
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Synonyms | TRK-820 |
AHFS/Drugs.com | International Drug Names |
Routes of administration | intravenous |
ATC code | |
Identifiers | |
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CAS Number | |
PubChem CID | |
IUPHAR/BPS | |
ChemSpider | |
UNII | |
ChEMBL | |
E number | {{#property:P628}} |
ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value). |
Chemical and physical data | |
Formula | C28H32N2O5 |
Molar mass | 476.564 g/mol |
3D model (JSmol) | |
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WikiDoc Resources for Nalfurafine |
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Business |
Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Nalfurafine (INN and USAN;[1] also known as AC-820, TRK-820; trade name Remitch) is a κ-opioid receptor agonist marketed as a treatment for uremic pruritus in people undergoing hemodialysis.[2]
As of January 2010[update], it is also being investigated for the treatment of pruritus in patients with chronic liver disease.[3]
References
- ↑ Statement on a Nonproprietary Name adopted by the USAN Council
- ↑ "AC-820". Acologix. 2009.
- ↑ Clinical trial number NCT00638495 for "Phase II Study of TRK-820 Soft Capsules — Intractable Pruritus in Patients With Chronic Liver Disease" at ClinicalTrials.gov
- Pages with script errors
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- Morphinans
- Phenols
- Alcohols
- Amides
- Semisynthetic opioids
- Alkenes
- Furans
- Drug