Predicted protein targets (top 10)
| gene | UniProt | supporting neighbours | confidence | |
|---|---|---|---|---|
| ▸ | FFAR1 | O14842 | 4/20 | 0.50 |
| ▸ | SLC9A1 | P19634 | 1/20 | 0.48 |
| ▸ | HTR2A | P28223 | 1/20 | 0.47 |
| ▸ | HTR2C | P28335 | 1/20 | 0.47 |
| ▸ | HTR2B | P41595 | 1/20 | 0.47 |
| ▸ | KDM1A | O60341 | 2/20 | 0.47 |
| ▸ | CYP4F2 | P78329 | 3/20 | 0.44 |
| ▸ | CYP4A11 | Q02928 | 3/20 | 0.44 |
| ▸ | GPR88 | Q9GZN0 | 1/20 | 0.43 |
| ▸ | FFAR4 | Q5NUL3 | 1/20 | 0.42 |
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 | |
|---|---|---|---|---|
| SCHEMBL7655989 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL12915852 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL18272394 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL15196464 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL18272446 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL29488083 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL248385 | 1.00 | FFAR1 (0.50) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL15189650 | 0.98 | FFAR1 (0.49) | FFAR1SLC9A1HTR2AHTR2CHTR2B | |
| SCHEMBL814567 | 0.86 | SLC9A1 (0.48) | SLC9A1HTR2AHTR2CHTR2BKDM1A | |
| SCHEMBL247915 | 0.86 | SLC9A1 (0.48) | SLC9A1HTR2AHTR2CHTR2BKDM1A |
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 135 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| CN-117209393-A | Preparation method of aromatic cyclopropyl formamide | 泓博智源(开原)药业有限公司 | 2023-12-12 | — | — | CN | claimed |
| CN-110437092-B | Preparation method of ticagrelor key intermediate aromatic cyclopropane amide | 泓博智源(开原)药业有限公司 | 2022-06-10 | — | — | CN | claimed |
| WO-2013144295-A1 | SYNTHESIS OF 2-(3,4-DIFLUOROPHENYL)CYCLOPROPANAMINE DERIVATIVES AND SALTS | SANDOZ AG (CH) | 2013-10-03 | — | — | WO | claimed |
| EP-2644590-A1 | Synthesis of 2-(3,4-difluorophenyl)cyclopropanamine derivatives and salts | LEK Pharmaceuticals d.d. (SI) | 2013-10-02 | — | — | EP | claimed |
| US-8278475-B2 | Processes for the preparation of optically active intermediates | ASTRAZENECA AB (SE) | 2012-10-02 | — | — | US | claimed |
| US-20120136167-A1 | Processes For The Preparation Of Optically Active Intermediates | ASTRAZENECA AB (SE) | 2012-05-31 | — | — | US | claimed |
| US-20110190520-A1 | Process for the preparation of cyclopropyl carboxylic acid esters and derivatives | ASTRAZENECA AB (SE) | 2011-08-04 | — | — | US | claimed |
| US-20060258879-A1 | Process for the preparation of cyclopropyl carboxylic acid esters and derivatives | ASTRAZENECA AB (SE) | 2006-11-16 | — | — | US | claimed |
| CN-115894496-B | Preparation method of ticagrelor and intermediate thereof | 上海贝美医药科技有限公司 | 2025-03-21 | — | — | CN | disclosed |
| CN-117209393-A | Preparation method of aromatic cyclopropyl formamide | 泓博智源(开原)药业有限公司 | 2023-12-12 | — | — | CN | disclosed |
| CN-117209393-A | Preparation method of aromatic cyclopropyl formamide | 泓博智源(开原)药业有限公司 | 2023-12-12 | — | — | CN | disclosed |
| WO-2023223335-A1 | A METHOD FOR PREPARING (1S)-2-CHLORO-1-(3,4-DIFLUOROPHENYL) ETHANOL | AARTI PHARMALABS LIMITED (IN) | 2023-11-23 | — | — | WO | disclosed |
| WO-2023125846-A1 | COMPOUND FOR PREVENTING AND TREATING CORONAVIRUS INFECTION, CONJUGATE THEREOF AND METHOD THEREFOR | 苏州爱科百发生物医药技术有限公司 | 2023-07-06 | — | — | WO | disclosed |
| CN-115894496-A | Preparation method of ticagrelor and intermediate thereof | 上海贝美医药科技有限公司 | 2023-04-04 | — | — | CN | disclosed |
| US-7122695-B2 | Process for the preparation of cyclopropyl carboxylic acid esters and derivatives | ASTRAZENECA AB (SE) | 2006-10-17 | — | — | US | disclosed |
| US-20060041132-A1 | Novel triazolo pyrimidine compounds | ASTRAZENECA AB (SE) | 2006-02-23 | — | — | US | disclosed |
| EP-0996621-B1 | TRIAZOLO[4,5-d]PYRIMIDINE DERIVATIVES AS ANTI-THROMBOTIC AGENTS | ASTRAZENECA AB (SE) | 2003-10-01 | — | — | EP | disclosed |
| EP-1056749-B1 | NOVEL TRIAZOLO(4,5-d)PYRIMIDINE COMPOUNDS | ASTRAZENECA UK LTD (GB) | 2003-02-19 | — | — | EP | disclosed |
| US-6369064-B1 | MYOCARDIAL INFARCTION AND UNSTABLE ANGINA; P2T-RECEPTOR ANTAGONISTS; ANTITHROMBOTIC AGENTS; 7-(SUBSTITUTED AMINO) -5-(THIO)-3H-1,2,3-TRIAZOLO(4,5-D)PYRIMIDIN-3-YL) -CYCLOPENTANECARBOXAMIDES | ASTRAZENECA AB (SE) | 2002-04-09 | — | — | US | disclosed |
| US-6251910-B1 | 1,2,3-triazolo[4,5-d]pyrimidines as P2T receptor antagonists | ASTRAZENECA UK LIMITED (GB) | 2001-06-26 | — | — | 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 (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.
| Patent | Title | Text reads most about | Predicted target · text-rank |
|---|---|---|---|
| US-20060258879-A1 | Process for the preparation of cyclopropyl carboxylic acid esters and derivatives | MCCC2, DHPS, CYP3A4 | FFAR1 1263/4885SLC9A1 4322/4885HTR2A 3833/4885 |
| US-20060041132-A1 | Novel triazolo pyrimidine compounds | TYMS, TYMP, DPYD | FFAR1 4291/4885SLC9A1 4604/4885HTR2A 2776/4885 |
| US-20110190520-A1 | Process for the preparation of cyclopropyl carboxylic acid esters and derivatives | MCCC2, DHPS, CYP3A4 | FFAR1 1263/4885SLC9A1 4322/4885HTR2A 3833/4885 |
| US-20120136167-A1 | Processes For The Preparation Of Optically Active Intermediates | DHPS, CYP2S1, CYP1B1 | FFAR1 1117/4885SLC9A1 4566/4885HTR2A 315/4885 |
“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.