Predicted protein targets (top 20)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | SLC6A4 | P31645 | 1/20 | 0.59 |
| ▸ | CHRNA7 | P36544 | 1/20 | 0.46 |
| ▸ | ACHE | P22303 | 3/20 | 0.40 |
| ▸ | TDP1 | Q9NUW8 | 2/20 | 0.40 |
| ▸ | LMNA | P02545 | 2/20 | 0.39 |
| ▸ | ALDH1A1 | P00352 | 1/20 | 0.39 |
| ▸ | SMN1; SMN2 | Q16637 | 1/20 | 0.39 |
| ▸ | MAOA | P21397 | 2/20 | 0.39 |
| ▸ | MAOB | P27338 | 1/20 | 0.39 |
| ▸ | CA7 | P43166 | 1/20 | 0.39 |
| ▸ | CYP1A2 | P05177 | 3/20 | 0.36 |
| ▸ | CYP2D6 | P10635 | 2/20 | 0.36 |
| ▸ | CYP2C19 | P33261 | 2/20 | 0.36 |
| ▸ | CYP2A6 | P11509 | 1/20 | 0.36 |
| ▸ | TAAR1 | Q96RJ0 | 1/20 | 0.36 |
| ▸ | ALOX5 | P09917 | 1/20 | 0.35 |
| ▸ | TACR1 | P25103 | 2/20 | 0.35 |
| ▸ | ESR1 | P03372 | 1/20 | 0.34 |
| ▸ | PGR | P06401 | 1/20 | 0.34 |
| ▸ | CHRM2 | P08172 | 1/20 | 0.34 |
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 | |
|---|---|---|---|---|
| SCHEMBL3865060 | 1.00 | SLC6A4 (0.59) | SLC6A4CHRNA7ACHETDP1LMNA | |
| SCHEMBL8286101 | 1.00 | SLC6A4 (0.59) | SLC6A4CHRNA7ACHETDP1LMNA | |
| Hydrochloric Acid SCHEMBL4933575 | 0.98 | SLC6A4 (0.57) | SLC6A4CHRNA7ACHETDP1LMNA | |
| Hydrochloric Acid SCHEMBL4935216 | 0.98 | SLC6A4 (0.57) | SLC6A4CHRNA7ACHETDP1LMNA | |
| SCHEMBL23092069 | 0.89 | SLC6A4 (0.70) | SLC6A4TDP1LMNAALDH1A1CYP1A2 | |
| SCHEMBL20280630 | 0.88 | SLC6A4 (0.48) | SLC6A4CHRNA7LMNAALDH1A1SMN1; SMN2 | |
| SCHEMBL20209645 | 0.84 | SLC6A4 (0.46) | SLC6A4CHRNA7CYP1A2CYP2D6CYP2C19 | |
| SCHEMBL3668921 | 0.82 | CHRNA7 (0.42) | SLC6A4CHRNA7ACHETDP1MAOA | |
| SCHEMBL12056799 | 0.81 | SLC2A1 (0.43) | SLC6A4CHRNA7ACHETDP1MAOA | |
| SCHEMBL29172465 | 0.81 | SLC2A1 (0.43) | SLC6A4CHRNA7ACHETDP1MAOA |
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 40 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-11780826-B2 | Bisamide sarcomere activating compounds and uses thereof | AMGEN INC. (US) | 2023-10-10 | — | — | US | disclosed |
| EP-2809669-B1 | FUSED PYRROLEDICARBOXAMIDES AND THEIR USE AS PHARMACEUTICALS | SANOFI SA (FR) | 2017-02-01 | — | — | EP | disclosed |
| EP-3056202-A1 | BENZOPYRROLIDONE DERIVATIVES POSSESSING ANTIVIRAL AND ANTICANCER PROPERTIES | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) | 2016-08-17 | — | — | EP | disclosed |
| US-9284333-B2 | Fused pyrroledicarboxamides and their use as pharmaceuticals | SANOFI (FR) | 2016-03-15 | — | — | US | disclosed |
| EP-2809669-A1 | FUSED PYRROLEDICARBOXAMIDES AND THEIR USE AS PHARMACEUTICALS | SANOFI (FR) | 2014-12-10 | — | — | EP | disclosed |
| WO-2013113860-A1 | FUSED PYRROLEDICARBOXAMIDES AND THEIR USE AS PHARMACEUTICALS | SANOFI (FR) | 2013-08-08 | — | — | WO | disclosed |
| US-7576234-B2 | Michael-type addition of a nucleophile to a dialkyl 2-methylidenylpropan-1,3-dioate and the conversion of a ester moiety into an amino moiety; S)-2-methylcysteine; desferrithiocin | GENZYME CORPORATION (US) | 2009-08-18 | — | — | US | disclosed |
| EP-1529037-B1 | SYNTHESIS OF 2-ALKYLCYSTEINES, 2-(HYDROXYLATED PHENYL)-4-ALKYLTHIAZOLINE-4-CARBOXYLIC ACIDS AND DERIVATIVES THEREOF | GENZYME CORP (US) | 2009-07-15 | — | — | EP | disclosed |
| US-20080255081-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INC. (US) | 2008-10-16 | — | — | US | disclosed |
| US-20080132536-A1 | PYRAZOLO [3,4-B] PYRIDINE COMPOUNDS, AND THEIR USE AS PDE4 INHIBITORS | GLAXO GROUP LIMITED | 2008-06-05 | — | — | US | disclosed |
| US-20040132789-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | UNIVERSITY OF FLORIDA | 2004-07-08 | — | — | US | disclosed |
| US-20040082796-A1 | Synthesis of substituted thiazoline carboxylic acids | GENZYME CORPORATION | 2004-04-29 | — | — | US | disclosed |
| US-20040044220-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | UNIVERSITY OF FLORIDA | 2004-03-04 | — | — | US | disclosed |
| US-20040024224-A1 | Synthesis of 2-alkyl amino acids | GENZYME CORPORATION (US) | 2004-02-05 | — | — | US | disclosed |
| US-20040006224-A1 | Synthesis of 2-alkyl amino acids | GENZYME CORPORATION | 2004-01-08 | — | — | US | disclosed |
| US-20030236435-A1 | Synthesis of 2-alkylcysteine via substituted thiazoline ester | GENZYME CORPORATION | 2003-12-25 | — | — | US | disclosed |
| US-20030236434-A1 | Synthesis of 2-alkylcysteine via substituted thiazoline amide | GENZYME CORPORATION (US) | 2003-12-25 | — | — | US | disclosed |
| US-20030236404-A1 | Synthesis of 2-alkylcysteine via phase transfer catalysis | GENZYME CORPORATION | 2003-12-25 | — | — | US | disclosed |
| US-20030229231-A1 | Synthesis of 2-alkylcysteine | GENZYME CORPORATION | 2003-12-11 | — | — | US | disclosed |
| US-20030225287-A1 | Synthesis of chiral 2-alkyl amino acids | GENZYME CORPORATION | 2003-12-04 | — | — | US | 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 (13 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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20030225287-A1 | Synthesis of chiral 2-alkyl amino acids | FTH1, CISD2, PTMS | SLC6A4 391/4885CHRNA7 4852/4885ACHE 4735/4885 |
| US-20030236404-A1 | Synthesis of 2-alkylcysteine via phase transfer catalysis | DIMT1, ICMT, CNDP2 | SLC6A4 372/4885CHRNA7 4881/4885ACHE 4032/4885 |
| US-11780826-B2 | Bisamide sarcomere activating compounds and uses thereof | TNNI3, TNNT2, TNNC1 | SLC6A4 2425/4885CHRNA7 1027/4885ACHE 2341/4885 |
| US-20080132536-A1 | PYRAZOLO [3,4-B] PYRIDINE COMPOUNDS, AND THEIR USE AS PDE4 INHIBITORS | PDE4A, PDE4B, PDE4C | SLC6A4 2173/4885CHRNA7 809/4885ACHE 580/4885 |
| US-20030236435-A1 | Synthesis of 2-alkylcysteine via substituted thiazoline ester | FTH1, TFRC, CNDP2 | SLC6A4 553/4885CHRNA7 4770/4885ACHE 4134/4885 |
| US-20030229231-A1 | Synthesis of 2-alkylcysteine | FTH1, CISD2, CNDP2 | SLC6A4 1001/4885CHRNA7 4849/4885ACHE 4735/4885 |
| US-20040044220-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | TXNRD2, PRDX3, SOD1 | SLC6A4 3352/4885CHRNA7 4871/4885ACHE 4255/4885 |
| US-20040024224-A1 | Synthesis of 2-alkyl amino acids | PTMS, DNPEP, CNDP2 | SLC6A4 846/4885CHRNA7 4874/4885ACHE 4844/4885 |
| US-20080255081-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | TXNRD2, PRDX3, SOD1 | SLC6A4 3352/4885CHRNA7 4871/4885ACHE 4255/4885 |
| US-20040006224-A1 | Synthesis of 2-alkyl amino acids | ASNS, AAAS, FTH1 | SLC6A4 451/4885CHRNA7 4567/4885ACHE 4802/4885 |
| US-20030236434-A1 | Synthesis of 2-alkylcysteine via substituted thiazoline amide | CNDP2, FTH1, PTMS | SLC6A4 1092/4885CHRNA7 4869/4885ACHE 3826/4885 |
| US-20040132789-A1 | Antioxidant and radical scavenging activity of synthetic analogs of desferrithiocin | TXNRD2, SOD1, PRDX3 | SLC6A4 2968/4885CHRNA7 4879/4885ACHE 4411/4885 |
| US-20040082796-A1 | Synthesis of substituted thiazoline carboxylic acids | CPN1, NAT1, ME1 | SLC6A4 2874/4885CHRNA7 2045/4885ACHE 944/4885 |
“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.