Loperamide

Loperamide

SCHEMBL542589

CN(C)C(=O)C(CCN1CCC(O)(c2ccc(Cl)cc2)CC1)(c1ccccc1)c1ccccc1.[Cl-].[H+]

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

OPRM1

The experimentally established mechanism targets of Loperamide. 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
OPRM1 known ✓ P35372 10/20 0.96
DRD4 P21917 5/20 0.96
ADRA2A P08913 3/20 0.96
SLC6A4 P31645 3/20 0.96
DRD2 P14416 3/20 0.96
DRD3 P35462 3/20 0.96
MEN1 O00255 2/20 0.96
LMNA P02545 2/20 0.96
ADRB2 P07550 2/20 0.96
OPRD1 P41143 2/20 0.96
OPRK1 P41145 2/20 0.96
HTR2B P41595 2/20 0.96
SLC6A3 Q01959 2/20 0.96
KMT2A Q03164 2/20 0.96
SMN1; SMN2 Q16637 2/20 0.96
SIGMAR1 Q99720 2/20 0.96
HRH2 P25021 2/20 0.96
ADRA1A P35348 2/20 0.96
KCNH2 Q12809 2/20 0.96
SCN5A Q14524 2/20 0.96

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
Loperamide SCHEMBL8409779 0.98 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL12387663 0.98 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL28530 0.98 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL9068543 0.97 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL8409268 0.97 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL21327979 0.97 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL15048 0.97 OPRM1 (1.00) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL2346867 0.96 OPRM1 (0.98) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL5084617 0.95 OPRM1 (0.94) OPRM1DRD4ADRA2ASLC6A4DRD2
Loperamide SCHEMBL12470757 0.94 OPRM1 (0.92) OPRM1DRD4ADRA2ASLC6A4DRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION ERESINA LLC (US) 2026-04-16 US disclosed
US-12031977-B2 Ex vivo system for determining multiple drug-drug transporter interactions and methods of use thereof MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2024-07-09 US disclosed
CN-116672344-A Application of loperamide hydrochloride in preparation of medicine for treating Salmonella infection 吉林大学 2023-09-01 CN disclosed
US-20220273637-A1 NOVEL PFAR-INHIBITING COMPOUNDS Institut National de la Santé et de la Recherche Médicale (FR) 2022-09-01 US disclosed
CN-114441663-A Method for screening protein positive compounds by using solid phase microextraction affinity selection mass spectrum 中国科学院上海药物研究所 2022-05-06 CN disclosed
US-20210393645-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2021-12-23 US disclosed
US-20210231645-A1 METHODS AND COMPOSITIONS FOR INVESTIGATING MULTIPLE DRUG-DRUG TRANSPORTER INTERACTIONS MASSACHUSETTS INSTITUTE OF TECHNOLOGY 2021-07-29 US disclosed
CN-112755072-A Application of two formulas in preparation of medicine for preventing and treating constipation 天津中医药大学 2021-05-07 CN disclosed
CN-110720466-A Application of loperamide hydrochloride in preparation of bactericide for preventing and treating plant diseases caused by plant pathogenic bacteria 青岛农业大学 2020-01-24 CN disclosed
US-20190262353-A1 TREATMENT FOR PROGRESSIVE MULTIPLE SCLEROSIS UTI LIMITED PARTNERSHIP (CA) 2019-08-29 US disclosed
US-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION BRAINCELLS, INC. (US) 2007-04-05 US disclosed
US-20070072899-A1 Method for treating drug and behavioral addictions THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE 2007-03-29 US disclosed
WO-2007025177-A2 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 WO disclosed
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION BRAINCELLS, INC. (US) 2007-03-01 US disclosed
US-6190691-B1 ADMINISTERING FORMULATION COMPRISING TUMOR NERCOSIS FACTOR (TNF) PRODUCTION-INHIBITORY AMOUNT OF A COMPOUND SELECTED FROM LOPERAMIDE AND DIPHENOXYLATE TO MAMMAL ADOLOR CORPORATION 2001-02-20 US disclosed
US-5962477-A USING LOPERAMIDE ADOLOR CORPORATION (US) 1999-10-05 US disclosed
EP-0937460-A2 Use of an antidiarrheal for the manufacture of a medicament for the treatment of inflammatory conditions Adolor Corporation (US) 1999-08-25 EP disclosed
EP-0757558-A4 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORP (US) 1999-06-16 EP disclosed
EP-0757558-A1 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORPORATION (US) 1997-02-12 EP disclosed
WO-1995027510-A1 SCREENING METHODS FOR INTEGUMENTAL INFLAMMATION MODULATING AGENTS ALZA CORPORATION (US) 1995-10-19 WO 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 (4 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-20070078083-A1 MODULATION OF NEUORGENESIS BY HDac INHIBITION DCX, BDNF, NTRK2 OPRM1 2413/4885DRD4 4415/4885ADRA2A 3369/4885
US-20070072899-A1 Method for treating drug and behavioral addictions SLC6A3, OPRD1, DRD2 OPRM1 12/4885DRD4 9/4885ADRA2A 513/4885
US-20070049576-A1 NEUROGENESIS BY MUSCARINIC RECEPTOR MODULATION CHRNB2, CHAT, CHRNB4 OPRM1 265/4885DRD4 1926/4885ADRA2A 317/4885
US-20260102359-A1 COMBINATION TREATMENT OF DERMAL AND TRANSDERMAL FIBROTIC DISEASES, DISORDERS AND ASSOCIATED PAIN AND INFLAMMATION COL2A1, COLGALT1, PLOD3 OPRM1 2633/4885DRD4 4301/4885ADRA2A 448/4885

“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.