Drug Information
Drug General Information | Top | |||
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Drug ID |
D0T2XU
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Former ID |
DAP000334
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Drug Name |
Promethazine
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Synonyms |
Antiallersin; Aprobit; Avomine; Camergan; Dimapp; Diphergan; Diprazin; Diprazine; Diprozin; Fargan; Fenazil; Fenetazina; Fenetazine; Genphen; Hiberna; Histargan; Iergigan; Isophenergan; Isopromethazine; Lercigan; Lergigan; Metaryl; Pelpica; Phargan; Phenargan; Phenerzine; Phensedyl; Pilothia; Pilpophen; Pipolphene; Proazaimine; Proazamine; Procit; Promacot; Promazinamide; Promergan; Promesan; Prometasin; Prometazin; Prometazina; Prometazine; Prometh; Promethacon; Promethaine; Promethazin; PromethazineHcl; Promethazinum; Promethegan; Promethiazine; Promezathine; Prorex; Protazine; Prothazin; Prothazine; Provigan; Pyrethia; Pyrethiazine; Remsed; Romergan; Rumergan; Tanidil; Thiergan; Valergine; Vallergine; Lilly 01516; Lilly 1516; RP 3277; SKF 1498; WY 509; A-91033; Atosil (TN); Avomine (TN); Fargan (TN); Farganesse (TN); Lergigan (TN); Phenergan (TN); Phenoject-50; Pro-50; Prometazina [INN-Spanish]; Promethazine [INN:BAN]; Promethazinum [INN-Latin]; Promethegan (TN); Prothiazine (TN); Receptozine (TN); Romergan (TN); Zipan-25; Dimethylamino-isopropyl-phenthiazin; Dimethylamino-isopropyl-phenthiazin [German]; Promethazine (JAN/INN)
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Drug Type |
Small molecular drug
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Indication | Nausea [ICD-11: MD90; ICD-10: R11] | Approved | [1], [2] | |
Therapeutic Class |
Antiallergic Agents
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Company |
Wyeth Pharmaceuticals
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Structure |
Download2D MOL |
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Formula |
C17H20N2S
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Canonical SMILES |
CC(CN1C2=CC=CC=C2SC3=CC=CC=C31)N(C)C
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InChI |
1S/C17H20N2S/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19/h4-11,13H,12H2,1-3H3
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InChIKey |
PWWVAXIEGOYWEE-UHFFFAOYSA-N
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CAS Number |
CAS 60-87-7
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PubChem Compound ID | ||||
PubChem Substance ID |
9608, 89596, 616468, 5236627, 7847560, 7980398, 8153034, 10529464, 11335180, 11360419, 11363762, 11366324, 11368886, 11372096, 11374835, 11377048, 11406271, 11461391, 11466916, 11468036, 11484535, 11486631, 11488656, 11490834, 11492963, 11494682, 14848899, 24434790, 26752304, 29224005, 46507798, 47216602, 47216603, 47216604, 47290955, 47588815, 47885231, 48110274, 48184815, 48259042, 48416477, 49698886, 49854482, 50105224, 56313067, 56313700, 56459433, 57322528, 75806049, 85088938
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ChEBI ID |
CHEBI:8461
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ADReCS Drug ID | BADD_D01854 ; BADD_D01855 | |||
SuperDrug ATC ID |
D04AA10; R06AD02
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SuperDrug CAS ID |
cas=000060877
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Interaction between the Drug and Microbe | Top | |||
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The Abundace of Studied Microbe(s) Regulated by Drug | ||||
The Order in the Taxonomic Hierarchy of the following Microbe(s): Bacteroidales | ||||
Studied Microbe: Bacteroides fragilis nontoxigenic
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Bacteroides fragilis nontoxigenic was decreased by Promethazine hydrochloride (adjusted p-values: 6.41E-03). | |||
Studied Microbe: Bacteroides uniformis
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Bacteroides uniformis was decreased by Promethazine hydrochloride (adjusted p-values: 7.56E-05). | |||
Studied Microbe: Bacteroides vulgatus
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Bacteroides vulgatus was decreased by Promethazine hydrochloride (adjusted p-values: 2.66E-06). | |||
Studied Microbe: Parabacteroides distasonis
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Parabacteroides distasonis was decreased by Promethazine hydrochloride (adjusted p-values: 5.04E-06). | |||
Studied Microbe: Parabacteroides merdae
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Parabacteroides merdae was decreased by Promethazine hydrochloride (adjusted p-values: 4.93E-07). | |||
The Order in the Taxonomic Hierarchy of the following Microbe(s): Verrucomicrobiales | ||||
Studied Microbe: Akkermansia muciniphila
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[3] | |||
Hierarchy | ||||
Abundance Change | Decrease | |||
Experiment Method | High-throughput screening | |||
Description | The abundance of Akkermansia muciniphila was decreased by Promethazine hydrochloride (adjusted p-values: 3.40E-03). |
Target and Pathway | Top | |||
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Target(s) | Histamine H1 receptor (H1R) | Target Info | Antagonist | [4], [5] |
KEGG Pathway | Calcium signaling pathway | |||
Neuroactive ligand-receptor interaction | ||||
Inflammatory mediator regulation of TRP channels | ||||
Panther Pathway | Histamine H1 receptor mediated signaling pathway | |||
Reactome | Histamine receptors | |||
G alpha (q) signalling events | ||||
WikiPathways | Monoamine GPCRs | |||
GPCRs, Class A Rhodopsin-like | ||||
IL-4 Signaling Pathway | ||||
Gastrin-CREB signalling pathway via PKC and MAPK | ||||
GPCR ligand binding | ||||
GPCR downstream signaling |
References | Top | |||
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REF 1 | URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 7282). | |||
REF 2 | FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 089013. | |||
REF 3 | Extensive impact of non-antibiotic drugs on human gut bacteria. Nature. 2018 Mar 29;555(7698):623-628. | |||
REF 4 | Intact cell binding for in vitro prediction of sedative and non-sedative histamine H1-receptor antagonists based on receptor internalization. J Pharmacol Sci. 2008 May;107(1):66-79. | |||
REF 5 | Inhibition by histamine H1 receptor antagonists of endogenous glibenclamide-sensitive K+ channels in follicle-enclosed Xenopus oocytes. Eur J Pharmacol. 1994 Jan 1;266(1):99-102. |
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