Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SMN1; SMN2 | Q16637 | 3/20 | 0.76 |
| ▸ | CASR | P41180 | 4/20 | 0.65 |
| ▸ | POLB | P06746 | 1/20 | 0.59 |
| ▸ | SIGMAR1 | Q99720 | 2/20 | 0.59 |
| ▸ | CYP3A4 | P08684 | 2/20 | 0.57 |
| ▸ | CHRM2 | P08172 | 1/20 | 0.57 |
| ▸ | HTR1A | P08908 | 1/20 | 0.57 |
| ▸ | ADRA2A | P08913 | 1/20 | 0.57 |
| ▸ | ADORA3 | P0DMS8 | 1/20 | 0.57 |
| ▸ | CHRM1 | P11229 | 1/20 | 0.57 |
| ▸ | SMPD1 | P17405 | 1/20 | 0.57 |
| ▸ | DRD1 | P21728 | 1/20 | 0.57 |
| ▸ | TBXA2R | P21731 | 1/20 | 0.57 |
| ▸ | SLC6A2 | P23975 | 1/20 | 0.57 |
| ▸ | SLC6A4 | P31645 | 1/20 | 0.57 |
| ▸ | ADRA1A | P35348 | 1/20 | 0.57 |
| ▸ | OPRM1 | P35372 | 1/20 | 0.57 |
| ▸ | DRD3 | P35462 | 1/20 | 0.57 |
| ▸ | HTR2B | P41595 | 1/20 | 0.57 |
| ▸ | SLC6A3 | Q01959 | 1/20 | 0.57 |
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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL774613 | 1.00 | SMN1; SMN2 (0.76) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| SCHEMBL79765 | 1.00 | SMN1; SMN2 (0.76) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| Hydrochloric Acid SCHEMBL27830673 | 0.98 | SMN1; SMN2 (0.79) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| SCHEMBL27939948 | 0.98 | SMN1; SMN2 (0.73) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| Hydrochloric Acid SCHEMBL5493749 | 0.98 | SMN1; SMN2 (0.79) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| Hydrochloric Acid SCHEMBL9635019 | 0.98 | SMN1; SMN2 (0.79) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| SCHEMBL11881252 | 0.96 | SMN1; SMN2 (0.70) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| SCHEMBL14469578 | 0.96 | SMN1; SMN2 (0.82) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| Diethylamine SCHEMBL27544555 | 0.91 | SMN1; SMN2 (0.65) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 | |
| SCHEMBL11877401 | 0.90 | CASR (0.73) | SMN1; SMN2CASRPOLBSIGMAR1CYP3A4 |
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 2489 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-3807293-B1 | PEPTIDES HAVING INHIBITORY ACTIVITY ON NEURONAL EXOCYTOSIS | ACRAF (IT) | 2026-01-14 | — | — | EP | claimed |
| EP-3807294-B1 | PEPTIDES HAVING INHIBITORY ACTIVITY ON MUSCARINIC RECEPTOR M3 | ACRAF (IT) | 2026-01-14 | — | — | EP | claimed |
| US-12377035-B2 | Peptides for inhibiting cholinergic calcitonin gene-related peptide (CGRP) and acetylcholine (ACH) release or inhibiting sensitization-mediated by TRPV1-mediated excitability in sensory neurons and methods of use thereof | AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO—A.C.R.A.F. S.p.A. (IT) | 2025-08-05 | — | — | US | claimed |
| EP-4274878-B1 | BASIC ASHLESS ADDITIVES AND LUBRICATING COMPOSITIONS CONTAINING SAME | LUBRIZOL CORP (US) | 2024-12-25 | — | — | EP | claimed |
| US-12102705-B2 | Peptides having inhibitory activity on muscarinic receptor M3 | AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO—A.C.R.A.F. S.p.A. (IT) | 2024-10-01 | — | — | US | claimed |
| CN-117886718-B | Preparation method of high-selectivity asymmetric urea compound and asymmetric urea compound | 内蒙古工业大学 | 2024-05-24 | — | — | CN | claimed |
| CN-117886718-A | Preparation method of high-selectivity asymmetric urea compound and asymmetric urea compound | 内蒙古工业大学 | 2024-04-16 | — | — | CN | claimed |
| CN-117383994-A | Preparation method of asymmetric urea compound and asymmetric urea compound | 内蒙古工业大学 | 2024-01-12 | — | — | CN | claimed |
| CN-113330004-B | Differential solubility driven asymmetric conversion process for substituted 2H-chromene-3-carboxylic acids | 株式会社AskAt | 2023-11-17 | — | — | CN | claimed |
| EP-4274878-A1 | BASIC ASHLESS ADDITIVES AND LUBRICATING COMPOSITIONS CONTAINING SAME | The Lubrizol Corporation (US) | 2023-11-15 | — | — | EP | claimed |
| EP-0845454-A1 | Method for the production of optically active cyclopropane derivatives | Ajinomoto Co., Inc. (JP) | 1998-06-03 | — | — | EP | claimed |
| EP-0843682-A1 | HIGH PURITY FORMULATIONS OF HIGHLY SUBSTITUTED LITHIUM AMIDE BASES | FMC CORPORATION (US) | 1998-05-27 | — | — | EP | claimed |
| US-5726308-A | High purity formulations of highly substituted lithium amide bases | FMC CORPORATION (US) | 1998-03-10 | — | — | US | claimed |
| WO-1997006173-A1 | HIGH PURITY FORMULATIONS OF HIGHLY SUBSTITUTED LITHIUM AMIDE BASES | FMC CORPORATION (US) | 1997-02-20 | — | — | WO | claimed |
| WO-1994026708-A1 | OPTICALLY ACTIVE 3-(1-(ALKYLAMINO))ALKYL PYRROLIDINES | THE UPJOHN COMPANY (US) | 1994-11-24 | — | — | WO | claimed |
| US-5302604-A | Squalene synthetase inhibitors, anticarcinogenic agents, zaragozic acid derivatives | MERCK & CO., INC. (US) | 1994-04-12 | — | — | US | claimed |
| US-5294627-A | Anticholesterol | MERCK & CO., INC. (US) | 1994-03-15 | — | — | US | claimed |
| WO-1993017557-A1 | CHOLESTEROL LOWERING COMPOUNDS PRODUCED BY DIRECTED BIOSYNTHESIS | MERCK & CO., INC. (US) | 1993-09-16 | — | — | WO | claimed |
| US-4584291-A | ANTIBIOTICS AND BETA-LACTAMASE INHIBITORS | BEECHAM GROUP P.L.C. (GB) | 1986-04-22 | — | — | US | claimed |
| EP-0064199-B1 | NOVEL SECALONIC ACID DERIVATIVES AND METHOD FOR PREPARING THEREOF | Asahi Kasei Kogyo Kabushiki Kaisha (JP) | 1985-08-21 | — | — | EP | claimed |