Etilevodopa

Etilevodopa

SCHEMBL584493

CCOC(=O)[C@@H](N)Cc1ccc(O)c(O)c1

nearest known ligand 0.64

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD3

The experimentally established mechanism targets of Etilevodopa. 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
DRD3 known ✓ P35462 1/20 0.50
ALOX15 P16050 6/20 0.64
KDM4E B2RXH2 4/20 0.64
HIF1A Q16665 4/20 0.64
HSD17B10 Q99714 4/20 0.64
SLC7A5 Q01650 4/20 0.64
RECQL P46063 3/20 0.64
USP2 O75604 2/20 0.64
ADORA3 P0DMS8 2/20 0.64
HTR2A P28223 2/20 0.64
PTGS2 P35354 2/20 0.64
TDP1 Q9NUW8 2/20 0.64
LCK P06239 2/20 0.64
PTGS1 P23219 2/20 0.64
EGFR P00533 1/20 0.64
FYN P06241 1/20 0.64
ALOX12 P18054 5/20 0.50
ALDH1A1 P00352 3/20 0.50
HPGD P15428 3/20 0.50
MEN1 O00255 2/20 0.50

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
Etilevodopa SCHEMBL1069939 1.00 ALOX15 (0.64) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL29634876 1.00 ALOX15 (0.64) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL7291700 0.98 ALOX15 (0.62) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL28278862 0.98 ALOX15 (0.62) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL7063390 0.98 ALOX15 (0.62) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL28209537 0.96 ALOX15 (0.59) ALOX15KDM4EHIF1AHSD17B10SLC7A5
Etilevodopa SCHEMBL28067523 0.94 ALOX15 (0.57) ALOX15KDM4EHIF1AHSD17B10SLC7A5
SCHEMBL6140024 0.88 ALOX15 (0.60) ALOX15KDM4EHIF1AHSD17B10SLC7A5
SCHEMBL15679070 0.88 ALOX15 (0.60) ALOX15KDM4EHIF1AHSD17B10SLC7A5
SCHEMBL11402716 0.87 SLC7A5 (0.48) ALOX15KDM4EHIF1AHSD17B10SLC7A5

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 1326 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4292653-B1 TARTARIC ACID SALTS OF [2-(3-FLUORO-5-METHANE-SULFONYLPHENOXY)ETHYL](PROPYL)AMINE IRL 790 AB (SE) 2026-03-18 EP claimed
US-12564596-B2 Agents and methods for modulating pathogen activity GRIFFITH UNIVERSITY (AU) 2026-03-03 US claimed
EP-3768263-B1 CONTINUOUS ADMINISTRATION OF PHARMACEUTICAL COMPOSITION FOR TREATMENT OF NEURODEGENERATIVE DISORDERS LOBSOR PHARMACEUTICALS AB (SE) 2025-10-29 EP claimed
US-12251368-B2 Continuous administration of pharmaceutical composition for treatment of neurodegenerative disorders INTRANCE MEDICAL SYSTEMS INC. (US) 2025-03-18 US claimed
US-20250057795-A1 LIQUID COMPOSITIONS, EYE DROPS, AND METHODS FOR TREATMENT OF EYE DISEASES USING Levodopa FORMULATIONS MARTENS JOHN A (US) 2025-02-20 US claimed
US-20250041257-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING LEVODOPA, A DOPAMINE DECARBOXYLASE INHIBITOR AND A COMT INHIBITOR AND METHOD OF ADMINISTRATION THEREOF INTRANCE MEDICAL SYSTEMS INC. 2025-02-06 US claimed
US-12156858-B2 Pharmaceutical compositions comprising levodopa, a dopamine decarboxylase inhibitor and a COMT inhibitor and method of administration thereof INTRANCE MEDICAL SYSTEMS INC. (US) 2024-12-03 US claimed
WO-2024218296-A1 COMBINATION TREATMENTS COMPRISING ADMINISTRATION OF LEUCINE-RICH REPEAT KINASE 2 (LRRK2) INHIBITORS H. LUNDBECK A/S (DK) 2024-10-24 WO claimed
EP-3870300-B1 IMIDAZO[1,5-A]PYRAZINE COMPOUNDS AS PDE2 INHIBITORS INTRA CELLULAR THERAPIES INC (US) 2024-07-10 EP claimed
EP-4356907-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING LEVODOPA, A DOPAMINE DECARBOXYLASE INHIBITOR AND A COMTINHIBITOR AND METHOD OF ADMINISTRATION THEREOF LobSor Pharmaceuticals Aktiebolag (SE) 2024-04-24 EP claimed
US-20050203130-A1 Use of D4 and 5-HT2A antagonists, inverse agonists or partial agonists PHARMANEUROBOOST N.V. (BE) 2005-09-15 US claimed
US-20050203124-A1 Compounds for the sustained reduction of body weight BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-09-15 US claimed
US-20050182090-A1 Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and a dopamine agonist BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-08-18 US claimed
WO-2005070427-A1 COMPOUNDS FOR THE SUSTAINED REDUCTION OF BODY WEIGHT NEUROSEARCH A/S (DK) 2005-08-04 WO claimed
WO-2005053796-A1 USE OF D4 AND 5-HT2A ANTAGONISTS, INVERSE AGONISTS OR PARTIAL AGONISTS B & B BEHEER NV (BE) 2005-06-16 WO claimed
EP-1541197-A1 Use of D4 and 5-HT2A antagonists, inverse agonists or partial agonists B&B Beheer NV (BE) 2005-06-15 EP claimed
EP-1507518-A1 COMBINATION IMMEDIATE RELEASE CONTROLLED RELEASE LEVODOPA/CARBIDOPA DOSAGE FORMS Impax Laboratories, Inc. (US) 2005-02-23 EP claimed
US-20040166159-A1 Pharmaceutical dosage forms having immediate and controlled release properties that contain an aromatic amino acid decarboxylase inhibitor and levodopa IMPAX LABORATORIES, INC. 2004-08-26 US claimed
WO-2003101432-A1 COMBINATION IMMEDIATE RELEASE CONTROLLED RELEASE LEVODOPA/CARBIDOPA DOSAGE FORMS IMPAX LABORATORIES, INC. (US) 2003-12-11 WO claimed
US-20030228360-A1 Combination immediate release controlled release levodopa/carbidopa dosage forms IMPAX LABORATORIES, INC. 2003-12-11 US 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 (8 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-12564596-B2 Agents and methods for modulating pathogen activity C3AR1, HTR3A, CHRM3 DRD3 128/4885ALOX15 3036/4885KDM4E 3481/4885
US-20050203124-A1 Compounds for the sustained reduction of body weight SLC6A2, SLC6A3, SLC6A4 DRD3 202/4885ALOX15 2157/4885KDM4E 1716/4885
US-12251368-B2 Continuous administration of pharmaceutical composition for treatment of neurodegenerative disorders COMT, DBH, DDC DRD3 301/4885ALOX15 1004/4885KDM4E 3114/4885
US-12156858-B2 Pharmaceutical compositions comprising levodopa, a dopamine decarboxylase inhibitor and a COMT inhibitor and method of administration thereof COMT, DDT, DDC DRD3 74/4885ALOX15 1508/4885KDM4E 2546/4885
US-20050182090-A1 Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and a dopamine agonist SLC6A2, SLC6A3, SLC18A2 DRD3 49/4885ALOX15 2151/4885KDM4E 3295/4885
US-20250057795-A1 LIQUID COMPOSITIONS, EYE DROPS, AND METHODS FOR TREATMENT OF EYE DISEASES USING Levodopa FORMULATIONS LOX, LOXL1, PDE6C DRD3 426/4885ALOX15 69/4885KDM4E 1805/4885
US-20050203130-A1 Use of D4 and 5-HT2A antagonists, inverse agonists or partial agonists HTR2A, HTR4, HTR5A DRD3 32/4885ALOX15 1074/4885KDM4E 1845/4885
US-20250041257-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING LEVODOPA, A DOPAMINE DECARBOXYLASE INHIBITOR AND A COMT INHIBITOR AND METHOD OF ADMINISTRATION THEREOF COMT, DDT, DDC DRD3 52/4885ALOX15 1795/4885KDM4E 2245/4885

“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.