Ranitidine

Ranitidine

SCHEMBL8594797

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

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 1.00
ACHE P22303 15/20 1.00
MEN1 O00255 1/20 1.00
SLC22A1 O15245 1/20 1.00
ABCB11 O95342 1/20 1.00
LMNA P02545 1/20 1.00
CHRM2 P08172 1/20 1.00
CHRM1 P11229 1/20 1.00
TSHR P16473 1/20 1.00
ADRA2C P18825 1/20 1.00
NFKB1 P19838 1/20 1.00
CHRM3 P20309 1/20 1.00
ATP4A P20648 1/20 1.00
PTGS1 P23219 1/20 1.00
SLC6A4 P31645 1/20 1.00
CYP2C19 P33261 1/20 1.00
ADRA1A P35348 1/20 1.00
PTGS2 P35354 1/20 1.00
ATP4B P51164 1/20 1.00
KMT2A Q03164 1/20 1.00

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 SCHEMBL826 1.00 ACHE (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL824 1.00 ACHE (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL825 1.00 ACHE (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL8796367 1.00 ACHE (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL8110889 0.99 RAD52 (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL1536277 0.99 ACHE (0.98) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL33298 0.99 RAD52 (1.00) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL21618415 0.99 ACHE (0.98) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL8488427 0.99 ACHE (0.98) ACHEMEN1SLC22A1ABCB11LMNA
Ranitidine SCHEMBL33299 0.99 RAD52 (1.00) ACHEMEN1SLC22A1ABCB11LMNA

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

Claimed or disclosed in 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2017139487-A1 METHODS, AGENTS, AND DEVICES FOR LOCAL NEUROMODULATION OF AUTONOMIC NERVES NORTHWIND MEDICAL, INC. (US) 2017-08-17 WO disclosed
WO-1998013073-A9 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDs AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN 1998-08-06 WO disclosed
WO-1998013073-A1 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDs AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1998-04-02 WO disclosed
WO-1996039126-A2 RANITIDINE SALTS ON MAGNESIUM TRISILICATE AS AN ADSORBATE WARNER-LAMBERT COMPANY (US) 1996-12-12 WO disclosed
EP-0649305-A1 BENZIMIDAZOLES FOR ALLEVIATING STOMACH ULCERS IN SWINE MONSANTO COMPANY (US) 1995-04-26 EP disclosed
WO-1994001107-A1 BENZIMIDAZOLES FOR ALLEVIATING STOMACH ULCERS IN SWINE MONSANTO COMPANY (US) 1994-01-20 WO disclosed
US-5187368-A Detection of microorganisms in a liquid sample to be tested GLAXO INC. (US) 1993-02-16 US disclosed
US-4806548-A 4-PHENYL-TETRAHYDROISOQUINOLINE ANTIDEPRESSANT, CIMETIDINE, AND RANITIDINE; HISTAMINE H-2-ANTAGONISTS T P O PHARMACHIM (BG) 1989-02-21 US disclosed