Famotidine

Famotidine

SCHEMBL188452

N=C(CCSCc1csc(N=C(N)N)n1)NS(N)(=O)=O

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH2

The experimentally established mechanism targets of Famotidine. 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 3/20 0.67
SLC22A2 O15244 2/20 0.67
CA12 O43570 2/20 0.67
SLC22A3 O75751 2/20 0.67
CA1 P00915 2/20 0.67
CA2 P00918 2/20 0.67
LMNA P02545 2/20 0.67
TSHR P16473 2/20 0.67
MAOA P21397 2/20 0.67
CA4 P22748 2/20 0.67
CA6 P23280 2/20 0.67
CA5A P35218 2/20 0.67
CA7 P43166 2/20 0.67
BLM P54132 2/20 0.67
PMP22 Q01453 2/20 0.67
POU5F1 Q01860 2/20 0.67
CA9 Q16790 2/20 0.67
SLC47A2 Q86VL8 2/20 0.67
CA13 Q8N1Q1 2/20 0.67
SLC47A1 Q96FL8 2/20 0.67

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
SCHEMBL11389410 0.94 HRH2 (0.62) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL11380937 0.90 HRH2 (0.63) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL10935664 0.88 HRH2 (0.69) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL11382761 0.87 HRH2 (0.60) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL11393006 0.86 HRH2 (0.58) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL23804965 0.85 HRH2 (0.74) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL23804963 0.85 HRH2 (0.74) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL10863148 0.85 HRH2 (0.59) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL11378486 0.84 CA2 (0.54) HRH2SLC22A2CA12SLC22A3CA1
SCHEMBL11246474 0.84 HRH2 (0.60) HRH2SLC22A2CA12SLC22A3CA1

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 106 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2021183259-A1 FAMOTIDINE AND FAMOTIDINE ANALOGS FOR CORONA VIRUS TREATMENT Nanopharmaceutics, Inc. (US) 2021-09-16 WO claimed
EP-0277900-A2 H2-Receptor antagonist compounds CENTRO MARGA PARA LA INVESTIGACION S.A. (ES) 1988-08-10 EP claimed
US-4283408-A Guanidinothiazole compounds, process for preparation and gastric inhibiting compositions containing them YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1981-08-11 US claimed
JP-56055383-A None JP disclosed
JP-58103312-A None JP disclosed
US-20260097023-A1 UNIT ORAL DOSE COMPOSITIONS COMPOSED OF IBUPROFEN OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF AND FAMOTIDINE OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF FOR THE TREATMENT OF ACUTE PAIN AND THE REDUCTION OF THE SEVERITY AND/OR RISK OF HEARTBURN AND/OR UPSET STOMACH SCHABAR RES ASSOCIATES LLC (US) 2026-04-09 US disclosed
US-12514846-B2 Unit oral dose compositions composed of ibuprofen or a pharmaceutically acceptable salt thereof and famotidine or a pharmaceutically acceptable salt thereof for the treatment of acute pain and the reduction of the severity and/or risk of heartburn and/or upset stomach SCHABAR RESEARCH ASSOCIATES LLC (US) 2026-01-06 US disclosed
US-12053457-B2 Unit oral dose compositions composed of ibuprofen and famotidine for the treatment of acute pain and the reduction of the severity and/or risk of heartburn SCHABAR RESEARCH ASSOCIATES LLC (US) 2024-08-06 US disclosed
US-12048690-B2 Unit oral dose compositions composed of naproxen sodium and famotidine for the treatment of acute pain and the reduction of the severity and/or risk of heartburn SCHABAR RESEARCH ASSOCIATES LLC (US) 2024-07-30 US disclosed
CN-117534630-A Method for refining high-purity famotidine to prepare B crystal form 重庆世森医药科技有限公司 2024-02-09 CN disclosed
US-20240041861-A1 COMPOSITIONS AND METHODS FOR TREATMENT AND PROPHYLAXIS OF VIRAL INFECTIONS NED BIOSYSTEMS INC (US) 2024-02-08 US disclosed
EP-0297019-B1 FAMOTIDINE POLYMORPHIC FORM AND PREPARATION THEREOF CENTRO MARGA PARA LA INVESTIGACION S.A. (ES) 1991-10-30 EP disclosed
US-5021582-A Acidifying alcoholic suspension, adding organic base, heating, diluting with chlorinated hydrrocarbon, cooling, filtering CENTRO MARGA PARA LA INVESTIGACION S.A. (ES) 1991-06-04 US disclosed
EP-0322335-A1 New-quanidino-thiazol compounds, their preparation, and use as intermediates of famotidine process CENTRO MARGA PARA LA INVESTIGACION S.A. (ES) 1989-06-28 EP disclosed
US-4609737-A DIHALOACETONE AND AMIDINOTHIOUREA YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1986-09-02 US disclosed
US-4562261-A 2-Guanidinothiazoline compounds, and process for preparing them YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1985-12-31 US disclosed
US-4497810-A Thiatriazine dioxides as gastric anti-secretory agents MERCK & CO., INC. (US) 1985-02-05 US disclosed
JP-S58103312-A AQUEOUS SOLUTION FOR INJECTION OF HARDLY SOLUBLE DRUG AND ITS PREPARATION YAMANOUCHI PHARMACEUT CO LTD 1983-06-20 JP disclosed
US-4283408-A Guanidinothiazole compounds, process for preparation and gastric inhibiting compositions containing them YAMANOUCHI PHARMACEUTICAL CO., LTD. (JP) 1981-08-11 US disclosed
JP-S5655383-A AMIZINE DERIVATIVE AND ITS PREPARATION YAMANOUCHI PHARMACEUT CO LTD 1981-05-15 JP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20260097023-A1 UNIT ORAL DOSE COMPOSITIONS COMPOSED OF IBUPROFEN OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF AND FAMOTIDINE OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF FOR THE TREATMENT OF ACUTE PAIN AND THE REDUCTION OF THE SEVERITY AND/OR RISK OF HEARTBURN AND/OR UPSET STOMACH SI, TNNC1, SLC10A2 HRH2 10/4885SLC22A2 722/4885CA12 1299/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.