Ecadotril

Ecadotril

SCHEMBL48974

CC(=O)SC[C@@H](Cc1ccccc1)C(=O)NCC(=O)OCc1ccccc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MME

The experimentally established mechanism targets of Ecadotril. 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
MME known ✓ P08473 6/20 0.47
CYP1A2 P05177 1/20 1.00
CYP3A4 P08684 1/20 1.00
CYP2D6 P10635 1/20 1.00
CYP2C9 P11712 1/20 1.00
CYP2C19 P33261 1/20 1.00
ABCC3 O15438 1/20 1.00
NR1I2 O75469 1/20 1.00
ABCB11 O95342 1/20 1.00
NR3C1 P04150 1/20 1.00
RARG P13631 1/20 1.00
CNR1 P21554 1/20 1.00
OPRK1 P41145 1/20 1.00
NR1H2 P55055 1/20 1.00
PPARA Q07869 1/20 1.00
NR1H3 Q13133 1/20 1.00
NR1I3 Q14994 1/20 1.00
HRH4 Q9H3N8 2/20 0.73
ECE1 P42892 2/20 0.47
ACE P12821 3/20 0.46

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
Dexecadotril SCHEMBL1649041 1.00 CYP1A2 (1.00) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
Racecadotril SCHEMBL373243 1.00 CYP1A2 (1.00) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
Racecadotril SCHEMBL16098141 0.99 CYP1A2 (0.98) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
Dexecadotril SCHEMBL28209442 0.94 CYP1A2 (0.88) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL10955802 0.94 PPARA (0.88) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
Racecadotril SCHEMBL16098344 0.91 CYP1A2 (0.82) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL8165601 0.89 CYP1A2 (0.80) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL10956150 0.89 CYP1A2 (0.80) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL10952774 0.87 CYP1A2 (0.78) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19
SCHEMBL10956142 0.87 CYP1A2 (0.77) CYP1A2CYP3A4CYP2D6CYP2C9CYP2C19

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 2865 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4637708-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE Novaliq GmbH (DE) 2025-10-29 EP claimed
WO-2024133913-A9 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2025-03-20 WO claimed
WO-2024133913-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2024-06-27 WO claimed
CN-117797061-B An antiaging composition containing boscalin, ecadotine and ergothioneine 广东万禧生物科技有限公司 2024-05-28 CN claimed
CN-117797061-A An antiaging composition containing boscalin, ecadotine and ergothioneine 广东万禧生物科技有限公司 2024-04-02 CN claimed
CN-116603014-A Formula and preparation method of antibacterial paste for treating acne pigment spot and skin-whitening 王兴刚 2023-08-18 CN claimed
EP-3503926-B1 NEW IMPROVED COMPOSITION OF RACECADOTRIL JOHNSON & JOHNSON CONSUMER INC (US) 2023-06-07 EP claimed
WO-2022265697-A1 COMPOSITIONS FOR TREATING VIRAL INFECTIONS AND METHODS FOR SAME Tiger Development, LLC (US) 2022-12-22 WO claimed
US-20220370360-A1 COMPOSITIONS FOR TREATING VIRAL INFECTIONS AND METHODS FOR SAME ACCESS TO ADVANCED HEALTH INSTITUTE 2022-11-24 US claimed
US-20210401751-A1 COMPOSITIONS FOR TREATING VIRAL INFECTIONS AND METHODS FOR SAME Tiger Development Inc. (US) 2021-12-30 US claimed
US-20040192584-A1 Combination of an aldosterone receptor antagonist and a neutral endopeptidase inhibitor PHARMACIA CORPORATION 2004-09-30 US claimed
WO-2004082636-A2 COMBINATION OF AN ALDOSTERONE RECEPTOR ANTAGONIST AND A NEUTRAL ENDOPEPTIDASE INHIBITOR PHARMACIA CORPORATION (US) 2004-09-30 WO claimed
WO-2003099279-A1 COMBINATION OF A DPP IV INHIBITOR AND A CARDIOVASCULAR COMPOUND NOVARTIS AG (CH) 2003-12-04 WO claimed
US-20020115655-A1 Such as S-(4-methoxybenzyl)-N-(2-(N',N'-dimethylamino)ethyl) thiosalicylamide; for treatment of cardiovascular disorders MASSACHUSETTS COLLEGE OF PHARMACY 2002-08-22 US claimed
US-20020028248-A1 RAPID-RELEASE MICRODISPERSIBLE ECADOTRIL PREPARATION BAYER AKTIENGESELLSCHAFT (DE) 2002-03-07 US claimed
EP-0820439-B1 METHOD FOR THE ASYMMETRICAL SYNTHESIS OF S-ACYLATED DERIVATIVES OF 2-MERCAPTOMETHYL 3-PHENYL PROPANOIC ACID, AND USE THEREOF FOR SYNTHESISING N-(MERCAPTOACYL) AMINO ACID DERIVATIVES BIOPROJET SOC CIV (FR) 2000-05-03 EP claimed
US-6013829-A REDUCING A MALONIC DIESTER, HYDRIDING TO OBTAIN A DIOL, ACETYLATING TO OBTAIN A MONOESTER, OXIDATION, SAPONIFICATION AND THIOACYLATING; ENZYME INHIBITORS; PROTEASES; OPTICS; ANTISECRETORY AND HYPOTENSIVE AGENTS SOCIETE CIVILE BIOPROJET (FR) 2000-01-11 US claimed
EP-0729936-B1 Process for the synthesis of alpha substituted acrylic acids and N-(mercaptoacyl)amino acids BIOPROJET SOC CIV (FR) 1999-07-07 EP claimed
EP-0914822-A1 RAPID-RELEASE MICRODISPERSIBLE ECADOTRIL PREPARATION Bayer Aktiengesellschaft (DE) 1999-05-12 EP claimed
WO-1993011797-A1 DRUG CONTAINING AN ATRIOPEPTIDASE INHIBITOR AND AT LEAST ONE CALCIC ANTAGONIST SOCIETE CIVILE BIOPROJET (FR) 1993-06-24 WO claimed