Hydroxyzine

Hydroxyzine

SCHEMBL41450

Cl.OCCOCCN1CCN([C@H](c2ccccc2)c2ccc(Cl)cc2)CC1

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Hydroxyzine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH1 known ✓ P35367 4/20 0.98
DRD3 P35462 5/20 0.98
USP2 O75604 3/20 0.98
KCNH2 Q12809 3/20 0.98
CYP2D6 P10635 3/20 0.98
DRD2 P14416 3/20 0.98
HRH2 P25021 2/20 0.98
HTR2A P28223 2/20 0.98
HTR2B P41595 2/20 0.98
CHRM2 P08172 2/20 0.98
ADRA2A P08913 2/20 0.98
ADRA1A P35348 2/20 0.98
ABCB11 O95342 1/20 0.98
ADRA2B P18089 1/20 0.98
ADRA2C P18825 1/20 0.98
DRD4 P21917 1/20 0.98
HTR7 P34969 1/20 0.98
OPRK1 P41145 1/20 0.98
HTR5A P47898 1/20 0.98
HTR6 P50406 1/20 0.98

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Hydroxyzine SCHEMBL491323 1.00 DRD3 (0.98) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL41448 1.00 DRD3 (0.98) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL4492 0.99 DRD3 (1.00) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL383277 0.99 DRD3 (1.00) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL3061159 0.99 DRD3 (1.00) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL4491 0.99 DRD3 (1.00) DRD3HRH1USP2KCNH2CYP2D6
Etodroxizine SCHEMBL9064076 0.98 DRD3 (0.98) DRD3HRH1USP2KCNH2CYP2D6
Etodroxizine SCHEMBL668191 0.98 DRD3 (0.98) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL28290521 0.98 DRD3 (0.98) DRD3HRH1USP2KCNH2CYP2D6
Hydroxyzine SCHEMBL15532242 0.96 DRD3 (0.95) DRD3HRH1USP2KCNH2CYP2D6

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 3081 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12178804-B2 Salts of cycloserine compounds and applications thereof SYNEURX INTERNATIONAL (TAIWAN) CORP. (TW) 2024-12-31 US claimed
CN-118021984-A Compound external preparation, preparation method and application thereof 南方医科大学 2024-05-14 CN claimed
CN-114019076-B Method for simultaneously measuring 5 components in compound hyprolfsteaine dechlorinated hydroxyzine capsules 苏州市药品检验检测研究中心 2024-04-09 CN claimed
WO-2022241985-A1 USE OF H1 HISTAMINE RECEPTOR ANTAGONIST IN PREPARATION OF DRUG FOR TREATING GLIOMA 温州医科大学附属第一医院 2022-11-24 WO claimed
CN-114414707-B Method and kit for detecting 19 drugs and metabolites thereof in blood by liquid chromatography tandem mass spectrometry 北京和合医学诊断技术股份有限公司 2022-07-22 CN claimed
CN-114414707-A Method and kit for detecting 19 drugs and metabolites thereof in blood by liquid chromatography tandem mass spectrometry 北京和合医学诊断技术股份有限公司 2022-04-29 CN claimed
US-20220047561-A1 SALTS OF CYCLOSERINE COMPOUNDS AND APPLICATIONS THEREOF SYNEURX INTERNATIONAL (TAIWAN) CORP. (TW) 2022-02-17 US claimed
US-20220031664-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING ANTIEMETICS AND ALPHA-2-ADRENERGIC RECEPTOR AGONISTS AND METHODS OF USING THE SAME FOR ANESTHESIOLOGICAL APPLICATIONS FIFTH THIRD BANK, NATIONAL ASSOCIATION, AS AGENT 2022-02-03 US claimed
US-20210338558-A1 USE OF COLLAGEN BINDING DOMAINS TO DELIVER PRODUCTS TO SKIN FABIUS BIOTECHNOLOGY (US) 2021-11-04 US claimed
CN-113384702-A Application of H1 histamine receptor antagonist in preparation of medicine for treating glioma 温州医科大学附属第一医院 2021-09-14 CN claimed
WO-2002026244-A2 COMPOSITIONS AND METHODS OF USE FOR EXTRACTS OF RUTACEAE PLANTS NEXT PHARMACEUTICALS, INC. (US) 2002-04-04 WO claimed
US-20010051184-A1 METHOD FOR USING SOLUBLE CURCUMIN TO INHIBIT PHOSPHORYLASE KINASE IN INFLAMMATORY DISEASES NEUVOLA II, LLC 2001-12-13 US claimed
US-6312728-B1 DRUG DELIVERY DEVICE WITH CORE, ENTERIC POLYMER AND COATING CASCADE DEVELOPMENT, INC. 2001-11-06 US claimed
EP-1094790-A1 SUSTAINED RELEASE PHARMACEUTICAL PREPARATION Cascade Development, Inc. (US) 2001-05-02 EP claimed
WO-2000070949-A1 METHOD FOR USING SOLUBLE CURCUMIN TO INHIBIT PHOSPHORYLASE KINASE IN INFLAMMATORY DISEASES HENG MADALENE C Y (US) 2000-11-30 WO claimed
WO-2000001369-A1 SUSTAINED RELEASE PHARMACEUTICAL PREPARATION CASCADE DEVELOPMENT, INC. (US) 2000-01-13 WO claimed
US-5968554-A DRUG DELIVERY WITH CORE AND PROTECTIVE COATING CASCADE DEVELOPMENT, INC. A SUBSIDIARY OF CARDINAL HEALTH, INC. (US) 1999-10-19 US claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
US-5053396-A For treatment of symptoms associated with excessive alcohol intake, analgesic; nicotinamide or nicotinamide adenine dinucleotide BLASS DAVID H (GB) 1991-10-01 US claimed
US-4889850-A Treatment of colic and teething THORNFELDT CARL R (US) 1989-12-26 US claimed