Cimetidine

Cimetidine

SCHEMBL534523

CN=C(NC#N)NCCSCc1nc[nH]c1C

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 Cimetidine. 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 1.00
CYP3A4 P08684 3/20 1.00
CYP2D6 P10635 3/20 1.00
LMNA P02545 2/20 1.00
TSHR P16473 2/20 1.00
SLC47A1 Q96FL8 2/20 1.00
MEN1 O00255 1/20 1.00
SLC22A2 O15244 1/20 1.00
CYP1A2 P05177 1/20 1.00
GLA P06280 1/20 1.00
ATP4A P20648 1/20 1.00
APEX1 P27695 1/20 1.00
PDE4A P27815 1/20 1.00
CYP2C19 P33261 1/20 1.00
ADRA1A P35348 1/20 1.00
ATP4B P51164 1/20 1.00
KMT2A Q03164 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
SLC47A2 Q86VL8 1/20 1.00
SLC22A8 Q8TCC7 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
Cimetidine SCHEMBL27313058 1.00 CYP3A4 (1.00) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL3735476 1.00 CYP3A4 (1.00) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL28681657 1.00 CYP3A4 (1.00) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL226031 1.00 CYP3A4 (1.00) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL1736444 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL28666399 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL28492534 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL1736443 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL22127097 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR
Cimetidine SCHEMBL28689625 0.99 CYP3A4 (0.98) CYP3A4CYP2D6HRH2LMNATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12491325-B2 Drug delivery devices and methods for administering substances to a body cavity by heterogenous aerosolization for treatment of binge-eating disorders and/or obesity APTARGROUP, INC. (US) 2025-12-09 US claimed
EP-4360512-B1 TRANSPORT PACKAGE FOR NEEDLED CHRISTMAS TREES VERWEYEN SEBASTIAN (DE) 2025-06-25 EP claimed
EP-4295670-B1 DEVICE FOR FIXING A IRRIGATION CANE FOR IRRIGATING TREE CROPS DESIGN AND PRINT 3D (FR) 2025-04-30 EP claimed
CN-119838022-A Amatoxin conjugates containing branched linkers 杭州多禧生物科技有限公司 2025-04-18 CN claimed
CN-114763335-B 4-Amide piperidine derivative and preparation method and application thereof 江苏谛奇医药科技有限公司 2025-03-18 CN claimed
CN-115379759-B Method for controlling pests, pest control agent composition, and pest control agent set 日本曹达株式会社 2025-03-14 CN claimed
US-12206795-B2 Lightweight attribute-based signcryption (ABSC) method for cloud-fog-assisted internet-of-things (IoT) QILU UNIVERSITY OF TECHNOLOGY (CN) 2025-01-21 US claimed
CN-119300838-A Oligosaccharide linker, linker-cargo comprising oligosaccharide linker and antibody conjugated drug with sugar chain remodelling, preparation method and use thereof 启德医药科技(苏州)有限公司 2025-01-10 CN claimed
CN-119232722-A System and method for micro-service cross-region registration and call 许继电气股份有限公司 2024-12-31 CN claimed
CN-119231643-A Distributed light Fu Qun group control method 国网天津市电力公司 2024-12-31 CN claimed
EP-0367484-B1 Carboxylic acid derivates GLAXO GROUP LTD (GB) 1994-02-16 EP claimed
EP-0279161-B1 A process for the preparation of cimetidine LEK TOVARNA FARMACEVTSKIH (SI) 1994-01-05 EP claimed
EP-0571463-A1 NOVEL CIMETIDINE POLYMORPH AND PROCESS FOR PREPARING SAME RICHTER GEDEON VEGYESZETI GYAR R.T. (HU) 1993-12-01 EP claimed
WO-1992014713-A1 NOVEL CIMETIDINE POLYMORPH AND PROCESS FOR PREPARING SAME Richter Gedeon Vegyészeti Gyár Rt. (HU) 1992-09-03 WO claimed
EP-0261818-B1 PROCESS FOR PREPARATION OF GUANIDINE DERIVATIVE MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1991-12-11 EP claimed
US-4973703-A ACTIVATED CARBON IN WATER IN PRESENCE OR ORGANIC ACID MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1990-11-27 US claimed
US-4808726-A REACTING N-CYANO-N*-METHYL-N\"-(2-(BUTANE-2,3-DIONYL) THIOETHYL) GUANIDINE WITH AMMONIUM SALT OF A CARBOXYLIC ACID AND FORMALDEHYDE MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1989-02-28 US claimed
EP-0261818-A1 Process for preparation of guanidine derivative MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1988-03-30 EP claimed
EP-0224612-A1 Process for the preparation of N-cyano-N'-methyl-N''[2-(5-methylimidazol-4-ylmethylthio)-ethyl]-guanidine HEUMANN PHARMA GMBH & CO (DE) 1987-06-10 EP claimed
EP-0046290-B1 SYNERGISTIC COMBINATION OF (R,S)ALPHA-FLUOROMETHYLHISTIDINE AND CIMETIDINE AS AN ANTI-ULCER AGENT MERCK & CO. INC. (US) 1985-01-02 EP claimed

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-12491325-B2 Drug delivery devices and methods for administering substances to a body cavity by heterogenous aerosolization for treatment of binge-eating disorders and/or obesity GCG, VAPA, GABRG2 HRH2 2029/4885CYP3A4 1107/4885CYP2D6 801/4885

“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.