Hlorfenamin

Hlorfenamin
Klinički podaci
Prodajno ime	Aller-Chlor, Allergican, Allergisan, Antagonate
Drugs.com	Monografija
Način primene	Oralno
Farmakokinetički podaci
Poluvreme eliminacije	21-27 h
Identifikatori
CAS broj	132-22-9
ATC kod	R06AB02 (WHO), R06AB04
PubChem	CID 2725
IUPHAR/BPS	1213
DrugBank	DB01114
ChemSpider	2624
KEGG	C06905
ChEBI	CHEBI:52010
ChEMBL	CHEMBL505
Hemijski podaci
Formula	C16H19ClN2
Molarna masa	274,788
	SMILES CN(C)CCC(C1=CC=C(Cl)C=C1)C1=CC=CC=N1; ;
	InChI InChI=1S/C16H19ClN2/c1-19(2)12-10-15(16-5-3-4-11-18-16)13-6-8-14(17)9-7-13/h3-9,11,15H,10,12H2,1-2H3 ; Key:SOYKEARSMXGVTM-UHFFFAOYSA-N ;
Fizički podaci
Tačka ključanja	142 °C (288 °F)

Hlorfenamin je organsko jedinjenje, koje sadrži 16 atoma ugljenika i ima molekulsku masu od 274,788 Da.^[1]^[2]

Osobine

Osobina	Vrednost
Broj akceptora vodonika	2
Broj donora vodonika	0
Broj rotacionih veza	5
Particioni koeficijent^[3] (ALogP)	3,7
Rastvorljivost^[4] (logS, log(mol/L))	-5,0
Polarna površina^[5] (PSA, Å²)	16,1

Reference

^ Knox, C.; Law, V.; Jewison, T.; Liu, P.; Ly, S.; Frolkis, A.; Pon, A.; Banco, K.; Mak, C.; Neveu, V.; Djoumbou, Y.; Eisner, R.; Guo, A. C.; Wishart, D. S. (2011). . „DrugBank 3.0: A comprehensive resource for 'Omics' research on drugs”. Nucleic Acids Research. 39 (Database issue): D1035—D1041. PMC 3013709 . PMID 21059682. doi:10.1093/nar/gkq1126.
^ Wishart, David S.; Knox, Craig; Guo, An Chi; Cheng, Dean; Shrivastava, Savita; Tzur, Dan; Gautam, Bijaya; Hassanali, Murtaza (2008). . „DrugBank: A knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—D906. PMC 2238889 . PMID 18048412. doi:10.1093/nar/gkm958.
^ Ghose, Arup K.; Viswanadhan, Vellarkad N.; Wendoloski, John J. (1998). . „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of ALOGP and CLOGP Methods”. The Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o.
^ Tetko, Igor V.; Tanchuk, Vsevolod Yu.; Kasheva, Tamara N.; Villa, Alessandro E. P. (2001). . „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Journal of Chemical Information and Computer Sciences. 41 (6): 1488—1493. PMID 11749573. doi:10.1021/ci000392t.
^ Ertl, Peter; Rohde, Bernhard; Selzer, Paul (2000). . „Fast Calculation of Molecular Polar Surface Area as a Sum of Fragment-Based Contributions and Its Application to the Prediction of Drug Transport Properties”. Journal of Medicinal Chemistry. 43 (20): 3714—3717. PMID 11020286. doi:10.1021/jm000942e.

Literatura

Hardman JG, Limbird LE, Gilman AG (2001). Goodman & Gilman's The Pharmacological Basis of Therapeutics (10. изд.). New York: McGraw-Hill. ISBN 0071354697. doi:10.1036/0071422803.
Thomas L. Lemke; David A. Williams, ур. (2007). Foye's Principles of Medicinal Chemistry (6. изд.). Baltimore: Lippincott Willams & Wilkins. ISBN 0781768799.

Spoljašnje veze

Chlorphenamine

Molimo Vas, obratite pažnju na važno upozorenje
u vezi sa temama iz oblasti medicine (zdravlja).

[1] Knox, C.; Law, V.; Jewison, T.; Liu, P.; Ly, S.; Frolkis, A.; Pon, A.; Banco, K.; Mak, C.; Neveu, V.; Djoumbou, Y.; Eisner, R.; Guo, A. C.; Wishart, D. S. (2011). . „DrugBank 3.0: A comprehensive resource for 'Omics' research on drugs”. Nucleic Acids Research. 39 (Database issue): D1035—D1041. PMC 3013709 . PMID 21059682. doi:10.1093/nar/gkq1126.

[2] Wishart, David S.; Knox, Craig; Guo, An Chi; Cheng, Dean; Shrivastava, Savita; Tzur, Dan; Gautam, Bijaya; Hassanali, Murtaza (2008). . „DrugBank: A knowledgebase for drugs, drug actions and drug targets”. Nucleic Acids Research. 36 (Database issue): D901—D906. PMC 2238889 . PMID 18048412. doi:10.1093/nar/gkm958.

[3] Ghose, Arup K.; Viswanadhan, Vellarkad N.; Wendoloski, John J. (1998). . „Prediction of Hydrophobic (Lipophilic) Properties of Small Organic Molecules Using Fragmental Methods: An Analysis of ALOGP and CLOGP Methods”. The Journal of Physical Chemistry A. 102 (21): 3762—3772. Bibcode:1998JPCA..102.3762G. doi:10.1021/jp980230o.

[4] Tetko, Igor V.; Tanchuk, Vsevolod Yu.; Kasheva, Tamara N.; Villa, Alessandro E. P. (2001). . „Estimation of Aqueous Solubility of Chemical Compounds Using E-State Indices”. Journal of Chemical Information and Computer Sciences. 41 (6): 1488—1493. PMID 11749573. doi:10.1021/ci000392t.

[5] Ertl, Peter; Rohde, Bernhard; Selzer, Paul (2000). . „Fast Calculation of Molecular Polar Surface Area as a Sum of Fragment-Based Contributions and Its Application to the Prediction of Drug Transport Properties”. Journal of Medicinal Chemistry. 43 (20): 3714—3717. PMID 11020286. doi:10.1021/jm000942e.

[1]

[2]

[3]

[4]

[5]

p r u Modulatori sigma receptora
σ₁	Agonisti: 3-PPP 4-PPBP 5-MeO-DMT Alazocin (SKF-10047) Amantadin ANAVEX2-73 Arketamin BD-737 BD-1052 Kaptodiam Citalopram CGRP Kloperastin Kokain Kutamezin (SA-4503) Ciklazocin Dehidroepiandrosteron (DHEA) (prasteron) Dehidroepiandrosteron sulfat (DHEA-S) (prasteron sulfat) Dekstralorfan Dekstrometorfan (DXM) Dekstrorfan (DXO) Dimemorfan Dimetiltriptamin (DMT) Ditolilgvanidin (DTG) Donepezil Eliprodil Escitalopram Fabomotizol (afobazol) Fluoksetin Fluvoksamin Ifenprodil Igmesin (JO-1784) IPAB Ketamin L-687384 MDMA (midomafetamin) Memantin Metamfetamin Metoksetamin Metilfenidat Nepinalon Neuropeptid Y Noskapin OPC-14523 Opipramol Pentazocin Pentoksiverin (karbetapentan) PRE-084 Pregnenolon Pregnenolon sulfat Pridopidin Racemetorfan (metorfan) Racemorfan (morfanol) UMB-23 UMB-82 Antagonisti: 3-PPP AC-927 BD-1008 BD-1031 BD-1047 BD-1060 BD-1063 BD-1067 BMY-14802 (BMS-181100) CM-156 Dup-734 E-5842 E-52862 (S1RA) Haloperidol LR-132 LR-172 MS-377 NE-100 NPC-16377 Panamesin (EMD-57455) PD-144418 Pentazocin Progesteron Rimkazol (BW-234U) Sertralin SR-31742A Alosterni modulatori: Fenitoin; Pozitivni: Metilfenilpiracetam SOMCL-668 Nepoznati/nerazvrstani: 3-Metoksidekstralorfan 3-MeO-PCP 4C-T-2 4-IBP 4-IPBS 4-MeO-PCP 5-MeO-DALT 5-MeO-DiPT Amitriptilin Azidopamil Hlorpromazin Klemastin Klomipramin Klorgilin D-Deprenil DiPT DPT Ibogain Imipramin KCR-12-83.1 Nemonaprid Noribogain RHL-033 RS-67,333 RTI-55 Šafran Safinamid Selegilin Spipetijan Trifluoperazin W-18 YKP10A
σ₂	Agonisti: 3-PPP Arketamin BD-1047 BD1063 Ditolilgvanidin (DTG) DKR-1005 DKR-1051 Haloperidol Ifenprodil Ketamin MDMA (midomafetamin) Metamfetamin OPC-14523 Opipramol PB-28 Fenciklidin Siramesin (Lu 28-179) UKH-1114 Antagonisti: AC-927 BD-1008 BD-1067 CM-156 CT-1812 LR-172 MIN-101 Panamesin (EMD-57455) SAS-0132 Nepoznati/nerazvrstani: 3-Metoksidekstralorfan 3-MeO-PCE 4-MeO-PCP 5-MeO-DALT 5-MeO-DiPT Klemastin DiPT DPT Ibogain Nemonaprid Nepinalon Noribogain Pentazocin RS-67,333 Safinamid TMA UMB-23 UMB-82 W-18
Neraz- vrstani	Agonisti: Berberin Etilketazocin Forfit Metafit Nalbufin Naluzotan Tapentadol Tenociklidin Antagonisti: AHD1 AZ66 Lamotrigin Nalokson SM-21 UMB-100 UMB-101 UMB-103 UMB-116 YZ-011 YZ-069 YZ-185 Alosterni modulatori: SKF-83959 Nepoznati/nerazvrstani: 18-Metoksikoronaridin BMY-13980 Butaklamol Karamifen Karvotrolin Hlorfenamin (hlorfeniramin) Hlorpromazin Cinarizin Cinuperon Klocapramin Dezocin EMD-59983 Hipericin (kantarion) Flufenazin Gevotrolin (WY-47384) Mepiramin (pirilamin) Molindon Perfenazin Pimozid Proadifen Prometazin Propranolol Hinidin Remoksiprid SL 82.0715 SR-31747A Tiospiron (BMY-13859) Venlafaksin