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Details

Stereochemistry EPIMERIC
Molecular Formula C76H52O46.C16H20N2
Molecular Weight 1941.5419
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENIRAMINE TANNATE

SMILES

CN(C)CCC(C1=CC=CC=C1)C2=CC=CC=N2.OC3=CC(=CC(O)=C3O)C(=O)OC4=CC(=CC(O)=C4O)C(=O)OC[C@H]5O[C@@H](OC(=O)C6=CC(O)=C(O)C(OC(=O)C7=CC(O)=C(O)C(O)=C7)=C6)[C@H](OC(=O)C8=CC(O)=C(O)C(OC(=O)C9=CC(O)=C(O)C(O)=C9)=C8)[C@@H](OC(=O)C%10=CC(O)=C(O)C(OC(=O)C%11=CC(O)=C(O)C(O)=C%11)=C%10)[C@@H]5OC(=O)C%12=CC(O)=C(O)C(OC(=O)C%13=CC(O)=C(O)C(O)=C%13)=C%12

InChI

InChIKey=ROWUOBMEOCWIMN-HBNMXAOGSA-N
InChI=1S/C76H52O46.C16H20N2/c77-32-1-22(2-33(78)53(32)92)67(103)113-47-16-27(11-42(87)58(47)97)66(102)112-21-52-63(119-72(108)28-12-43(88)59(98)48(17-28)114-68(104)23-3-34(79)54(93)35(80)4-23)64(120-73(109)29-13-44(89)60(99)49(18-29)115-69(105)24-5-36(81)55(94)37(82)6-24)65(121-74(110)30-14-45(90)61(100)50(19-30)116-70(106)25-7-38(83)56(95)39(84)8-25)76(118-52)122-75(111)31-15-46(91)62(101)51(20-31)117-71(107)26-9-40(85)57(96)41(86)10-26;1-18(2)13-11-15(14-8-4-3-5-9-14)16-10-6-7-12-17-16/h1-20,52,63-65,76-101H,21H2;3-10,12,15H,11,13H2,1-2H3/t52-,63-,64+,65-,76+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C76H52O46
Molecular Weight 1701.1985
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula C16H20N2
Molecular Weight 240.3434
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description
Curator's Comment: Description was created based on several sources, including http://www.druginfosys.com/drug.aspx?drugcode=561&type=1 | https://www.drugbank.ca/drugs/DB01620

Pheniramine is an antihistamine used to treat allergic conditions such as hay fever or urticaria. It is generally sold in combination with other medications, rather than as a stand-alone drug. Allergies are caused by an excessive type 1 hypersensitivity response of the body to allergens, mediated by inappropriate histamine signalling. By inhibiting the binding of histamine, antihistamines decrease the normal histamine response from cells, consequently decreasing allergic symptoms. Antihistamines such as pheniramine appear to compete with histamine for histamine H1- receptor sites on effector cells. The antihistamines antagonize those pharmacological effects of histamine which are mediated through activation of H1- receptor sites and thereby reduce the intensity of allergic reactions and tissue injury response involving histamine release. Antihistamines suppress the histamine-induced wheal (swelling) and flare (vasodilation) response by blocking the binding of histamine to its receptors on nerves, vascular smooth muscle, glandular cells, endothelium, and mast cells. They effectively exert competitive antagonism of histamine for H1-receptors. Pheniramine is marketed under the trade name Avil and Visine-A among others).

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
7.5 null [pKi]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
AVIL

Approved Use

Allergic conditions including hay fever, drug rashes, angioneurotic oedema, serum sickness, allergic conjunctivitis, food allergy etc. · Conditions of the respiratory tract that are accompanied by increased secretion, including vasomotor rhinitis and acute rhinitis. · All itching skin conditions, including neurodermatitis, eczema of any origin, lichen planus, acute and chronic urticaria, pruritis of the anus or genitals, pruritus in icterus and diabetes, radiation sickness etc. · Prevention and treatment of motion sickness. · Prevention and treatment of nausea, vomiting and vertigo due to Menière’s disease and other labyrinthine disturbances.
Palliative
Visine-A

Approved Use

Visine-A is an antihistamine/redness reliever eye drop, formerly available by prescription only, that provides temporary relief of itchy, red eyes due to pollen, ragweed, grass, animal hair and dander.
Primary
AVIL

Approved Use

Allergic conditions including hay fever, drug rashes, angioneurotic oedema, serum sickness, allergic conjunctivitis, food allergy etc. · Conditions of the respiratory tract that are accompanied by increased secretion, including vasomotor rhinitis and acute rhinitis. · All itching skin conditions, including neurodermatitis, eczema of any origin, lichen planus, acute and chronic urticaria, pruritis of the anus or genitals, pruritus in icterus and diabetes, radiation sickness etc. · Prevention and treatment of motion sickness. · Prevention and treatment of nausea, vomiting and vertigo due to Menière’s disease and other labyrinthine disturbances.
Preventing
AVIL

Approved Use

Allergic conditions including hay fever, drug rashes, angioneurotic oedema, serum sickness, allergic conjunctivitis, food allergy etc. · Conditions of the respiratory tract that are accompanied by increased secretion, including vasomotor rhinitis and acute rhinitis. · All itching skin conditions, including neurodermatitis, eczema of any origin, lichen planus, acute and chronic urticaria, pruritis of the anus or genitals, pruritus in icterus and diabetes, radiation sickness etc. · Prevention and treatment of motion sickness. · Prevention and treatment of nausea, vomiting and vertigo due to Menière’s disease and other labyrinthine disturbances.
Primary
AVIL

Approved Use

Allergic conditions including hay fever, drug rashes, angioneurotic oedema, serum sickness, allergic conjunctivitis, food allergy etc. · Conditions of the respiratory tract that are accompanied by increased secretion, including vasomotor rhinitis and acute rhinitis. · All itching skin conditions, including neurodermatitis, eczema of any origin, lichen planus, acute and chronic urticaria, pruritis of the anus or genitals, pruritus in icterus and diabetes, radiation sickness etc. · Prevention and treatment of motion sickness. · Prevention and treatment of nausea, vomiting and vertigo due to Menière’s disease and other labyrinthine disturbances.
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
274 ng/mL
30.5 mg single, oral
dose: 30.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PHENIRAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
5768 ng × h/mL
30.5 mg single, oral
dose: 30.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PHENIRAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
17 h
30.5 mg single, oral
dose: 30.5 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PHENIRAMINE plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
[Antimycobacterial antihistaminics].
1989 Aug
Role of central histaminergic system in lorazepam withdrawal syndrome in rats.
2001 Apr
Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mixtures.
2001 Apr
pH-independent large-volume sample stacking of positive or negative analytes in capillary electrophoresis.
2001 Jan
Efficacy and safety of rectal thiopental, intramuscular cocktail and rectal midazolam for sedation in children undergoing neuroimaging.
2002 Dec
Pre-treatment of anaphylaxis, does it really work?
2005 Dec
A case of pheniramine dependence.
2005 Mar
A comparison of the clinical efficacy of pheniramine maleate/naphazoline hydrochloride ophthalmic solution and olopatadine hydrochloride ophthalmic solution in the conjunctival allergen challenge model.
2005 May
Antiradical effects of antihistamines in human blood. Structure-activity relationship.
2006 Apr
Extra- and intracellular formation of reactive oxygen species by human neutrophils in the presence of pheniramine, chlorpheniramine and brompheniramine.
2006 Dec
Enantioselective analysis of pheniramine in urine by charged CD-mediated CZE provided with a fiber-based DAD and an on-line sample pretreatment by capillary ITP.
2007 Aug
Intraoperative anaphylaxis with a complicated pulmonary hydatid cyst.
2007 Feb
Chiral separation of alkylamine antihistamines in pharmaceuticals by capillary isotachophoresis with charged cyclodextrin.
2007 Nov
The lollipop with strawberry aroma may be promising in reduction of infusion-related nausea and vomiting during the infusion of cryopreserved peripheral blood stem cells.
2008 Dec
[Toxic epidermal necrolysis following dorzolamide eyedrops].
2008 Jan
Techniques of skin biopsy and practical considerations.
2008 Jul
Pheniramines and oxidative burst of blood phagocytes during ischaemia/reperfusion.
2009 Apr
Protective effect of pheniramines against mesenteric ischaemia/reperfusion-induced injury.
2009 Apr
In vitro antibacterial activity of some systemic and topical antihistaminic preparations.
2009 Dec 1
Comparison of chiral separation of basic drugs in capillary electrophoresis and liquid chromatography using neutral and negatively charged cyclodextrins.
2009 Jul 10
Preparation and evaluation of orodispersible tablets of pheniramine maleate by effervescent method.
2009 Mar
In situ forming polymeric drug delivery systems.
2009 May
Simultaneous determination of pseudoephdrine, pheniramine, guaifenisin, pyrilamine, chlorpheniramine and dextromethorphan in cough and cold medicines by high performance liquid chromatography.
2009 May 15
Halogenation effects of pheniramines on the complexation with beta-cyclodextrin.
2009 Oct 15
Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands.
2010 Dec 5
Substance use and addiction research in India.
2010 Jan
Severe pulmonary adverse effects in lymphoma patients treated with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) regimen plus rituximab.
2010 Mar
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Could also be used topically https://www.drugs.com/drp/pheniramine-maleate.html
Each Avil (Pheniramine maleate) tablet contains 45.3mg pheniramine maleate. In adults and children over 10 years of age, treatment is commenced with half a tablet taken up to three times daily. This dose may be increased to one tablet taken up to three times daily if required. Children 5-10 years of age: half a tablet up to three times daily. Avil tablets are not recommended in children under 5 years of age.
Route of Administration: Oral
Histamine (100 uM)-induced contractions was blocked by pheniramine (0.32 uM) by 74% in neonatal small intestinal smooth muscle of dilated pre-atretic part of intestinal atresia.
Substance Class Chemical
Created
by admin
on Fri Dec 15 20:19:00 UTC 2023
Edited
by admin
on Fri Dec 15 20:19:00 UTC 2023
Record UNII
8MIX3625C1
Record Status Validated (UNII)
Record Version
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Name Type Language
PHENIRAMINE TANNATE
WHO-DD  
Common Name English
PHENIRAMINE TANNATE [WHO-DD]
Common Name English
Code System Code Type Description
PUBCHEM
165411841
Created by admin on Fri Dec 15 20:19:00 UTC 2023 , Edited by admin on Fri Dec 15 20:19:00 UTC 2023
PRIMARY
SMS_ID
100000085683
Created by admin on Fri Dec 15 20:19:00 UTC 2023 , Edited by admin on Fri Dec 15 20:19:00 UTC 2023
PRIMARY
EVMPD
SUB03748MIG
Created by admin on Fri Dec 15 20:19:00 UTC 2023 , Edited by admin on Fri Dec 15 20:19:00 UTC 2023
PRIMARY
FDA UNII
8MIX3625C1
Created by admin on Fri Dec 15 20:19:00 UTC 2023 , Edited by admin on Fri Dec 15 20:19:00 UTC 2023
PRIMARY
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