Ranitidine

Ranitidine

SCHEMBL33298

CN/C(=C/[N+](=O)[O-])NCCSCc1ccc(CN(C)C)o1.Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH2

The experimentally established mechanism targets of Ranitidine. 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
HRH2 known ✓ P25021 1/20 0.98
RAD52 P43351 3/20 1.00
MAPT P10636 1/20 1.00
BLM P54132 1/20 1.00
ACHE P22303 15/20 0.98
MEN1 O00255 1/20 0.98
SLC22A1 O15245 1/20 0.98
ABCB11 O95342 1/20 0.98
LMNA P02545 1/20 0.98
CHRM2 P08172 1/20 0.98
CHRM1 P11229 1/20 0.98
TSHR P16473 1/20 0.98
ADRA2C P18825 1/20 0.98
NFKB1 P19838 1/20 0.98
CHRM3 P20309 1/20 0.98
ATP4A P20648 1/20 0.98
PTGS1 P23219 1/20 0.98
SLC6A4 P31645 1/20 0.98
CYP2C19 P33261 1/20 0.98
ADRA1A P35348 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
Ranitidine SCHEMBL8110889 1.00 RAD52 (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL5928192 1.00 RAD52 (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL33299 1.00 RAD52 (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL8819146 1.00 RAD52 (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL2228178 0.99 RAD52 (0.98) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL824 0.99 ACHE (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL8594797 0.99 ACHE (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL8796367 0.99 ACHE (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL825 0.99 ACHE (1.00) RAD52MAPTBLMACHEMEN1
Ranitidine SCHEMBL826 0.99 ACHE (1.00) RAD52MAPTBLMACHEMEN1

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 7238 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12601718-B2 Method for pretreating ranitidine hydrochloride sample Hunan Institute for Drug Inspection and Testing (CN) 2026-04-14 US claimed
US-20260076872-A1 POLYMER VIALS WITH SUBSTANTIALLY FLAT BOTTOMS AND INJECTION STRETCH BLOW MOLDING METHODS FOR MAKING THE SAME SIO2 MEDICAL PRODUCTS LLC (US) 2026-03-19 US claimed
EP-4654949-A1 USE OF VITAMIN E TPGS AS A TASTE MASKING AGENT FOR BITTER DRUGS Hyloris Developments SA (BE) 2025-12-03 EP claimed
US-20250242092-A1 SiOx BARRIER FOR PHARMACEUTICAL PACKAGE AND COATING PROCESS SIO2 MEDICAL PRODUCTS INC (US) 2025-07-31 US claimed
CN-119326718-B Production process of ranitidine hydrochloride injection 安徽长江药业有限公司 2025-04-22 CN claimed
CN-119751387-A Synthesis method of ranitidine Ding Zazhi A hydrochloride 江苏汉斯通药业有限公司 2025-04-04 CN claimed
US-12257371-B2 SiOx barrier for pharmaceutical package and coating process SIO2 MEDICAL PRODUCTS, LLC (US) 2025-03-25 US claimed
CN-119569687-A Preparation method of ranitidine hydrochloride small rod-shaped crystal habit 江苏正济药业股份有限公司 2025-03-07 CN claimed
EP-4255414-B1 COMPOSITION CONTAINING RANITIDINE HAVING A LOW IRON CONTENT OPELLA HEALTHCARE GROUP SAS (FR) 2025-02-05 EP claimed
CN-119326718-A Production process of ranitidine hydrochloride injection 安徽长江药业有限公司 2025-01-21 CN claimed
US-5219563-A Contacting synthetic cation exchange resin with ranitidine or salt to form complex GLAXO GROUP LIMITED (GB) 1993-06-15 US claimed
US-5102665-A Ranitidine or salts, monoalkali metal citrate, alkali or alkaline metal carbonates or bicarbonates for treatment of gastrointestinal disorder; antiinflammatory or/and antiallergic agent GLAXO GROUP LIMITED (GB) 1992-04-07 US claimed
US-5028432-A Nonaqueous Matrix of Glyceride and/or Mineral Oil or Paraffin GLAXO CANADA, INC. (CA) 1991-07-02 US claimed
CN-1039419-A PROCESS FOR PREPARATION OF FURAN DERIVATIVES GLAXO GROUP LTD (GB) 1990-02-07 CN claimed
CN-1037651-A DRUG ADSORBATES GLAXO GROUP LTD (GB) 1989-12-06 CN claimed
US-4880636-A STORAGE STABILITY, TRIACETIN PLASTICIZERS GLAXO INC., RESEARCH TRIANGLE PARK, NC A NC CORP. 1989-11-14 US claimed
EP-0320551-A1 Non-steroidal anti-inflammatory compositions protected against gastrointestinal injury with a combination of certain H1 and H2 receptor blockers Bristol-Myers Company (US) 1989-06-21 EP claimed
US-4757060-A Analgesic, H1, H2 receptor blockers BRISTOL-MYERS COMPANY (US) 1988-07-12 US claimed
US-4672133-A CRYSTALLIZATION UNDER CONTROLLED CONDITIONS GLAXO GROUP LIMITED (GB) 1987-06-09 US claimed
US-4521431-A HISTAMINE H2-ANTAGHONISTS, ANTIULCER, ANTIALLERGEN, AND ANTINFLAMMATORY AGENT GLAXO GROUP LIMITED (GB) 1985-06-04 US claimed