Known targets — ChEMBL curated mechanism
ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Pyrrolidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
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 | |
|---|---|---|---|---|
| Acetic Acid SCHEMBL29130314 | 0.97 | SMN1; SMN2 (0.47) | — | |
| Piperidine SCHEMBL10332243 | 0.97 | ALDH1A1 (0.56) | — | |
| Pyrrolidine SCHEMBL27499862 | 0.97 | ALDH1A1 (0.47) | — | |
| Piperidine SCHEMBL192668 | 0.97 | ALDH1A1 (0.56) | — | |
| Piperidine SCHEMBL29043025 | 0.97 | ALDH1A1 (0.56) | — | |
| Piperidine SCHEMBL1049754 | 0.94 | ALDH1A1 (0.53) | — | |
| Acetic Acid SCHEMBL9430014 | 0.93 | SMN1; SMN2 (0.50) | — | |
| Azetidine SCHEMBL2300503 | 0.93 | — | — | |
| Azetidine SCHEMBL30499018 | 0.93 | FFAR3 (0.54) | — | |
| Piperidine SCHEMBL15571721 | 0.91 | ALDH1A1 (0.50) | — |
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 233 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| US-20250362278-A1 | MASS SPECTROMETRY OF MRNA | MODERNATX, INC. (US) | 2025-11-27 | — | — | US | claimed |
| CN-119080615-A | Method for preparing long-chain dibasic acid or dibasic ester | 中国科学院大连化学物理研究所 | 2024-12-06 | — | — | CN | claimed |
| CN-118829629-A | Process for the preparation of 4-methyl-2-prop-2-yl-pyridine-3-carbonitrile | 美国安进公司 | 2024-10-22 | — | — | CN | claimed |
| EP-4426853-A1 | MASS SPECTROMETRY OF MRNA | ModernaTX, Inc. (US) | 2024-09-11 | — | — | EP | claimed |
| CN-113543706-B | Electrode comprising a conductive acrylate-based pressure sensitive adhesive | 汉高股份有限及两合公司 | 2024-07-23 | — | — | CN | claimed |
| CN-118235027-A | Ion conductive composition for thermal sensor | 汉高股份有限及两合公司 | 2024-06-21 | — | — | CN | claimed |
| WO-2023172858-A9 | A PROCESS FOR PREPARING 4-METHYL-2-PROPAN-2-YL-PYRIDINE-3-CARBONITRILE | AMGEN INC. (US) | 2024-05-16 | — | — | WO | claimed |
| EP-3935119-B1 | DRY ELECTRODE ADHESIVE | HENKEL AG & CO KGAA (DE) | 2024-01-24 | — | — | EP | claimed |
| US-11851392-B2 | Self-condensation of aldehydes | EASTMAN CHEMICAL COMPANY (US) | 2023-12-26 | — | — | US | claimed |
| WO-2023172858-A1 | A PROCESS FOR PREPARING 4-METHYL-2-PROPAN-2-YL-PYRIDINE-3-CARBONITRILE | AMGEN INC. (US) | 2023-09-14 | — | — | WO | claimed |
| EP-1745043-A1 | PROCESS FOR THE PREPARATION OF ROSIGLITAZONE | Medichem S.A. (ES) | 2007-01-24 | — | — | EP | claimed |
| WO-2005108394-A1 | PROCESS FOR THE PREPARATION OF ROSIGLITAZONE | MEDICHEM S.A. (ES) | 2005-11-17 | — | — | WO | claimed |
| US-6239300-B1 | Metallocene production process | PHILLIPS PETROLEUM COMPANY | 2001-05-29 | — | — | US | claimed |
| US-6028231-A | Process for preparing 2-methyl-4-(2,2,3-trimethyl-cyclopent-3-en-1-yl)-but-2-en-1-ol | HENKEL KOMMANDITGESELLSCHAFT AUF AKTIEN (DE) | 2000-02-22 | — | — | US | claimed |
| US-5955635-A | Process for the preparation of 4-(6'-methoxy-2'-naphthyl) butan-2-one | SECIFARMA S.P.A. (IT) | 1999-09-21 | — | — | US | claimed |
| US-4501918-A | ALDOL CONDENSATION OF ISOBUTYRALDEHYDE AND ACETONE IN PRESENCE OF BASIC CATALYST, CYCLIC DIMERIZATION, AND REDUCTION | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-02-26 | — | — | US | claimed |
| US-4493791-A | Substituted methyl isopropyl oxocyclohexane derivatives, organoleptic uses thereof and process for preparing same | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1985-01-15 | — | — | US | claimed |
| EP-0027948-B1 | TETRAHYDRO-FLUORENE COMPOUNDS, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THEREOF | MERCK & CO. INC. (US) | 1984-03-21 | — | — | EP | claimed |
| US-4400311-A | Substituted methyl isopropyl cyclohexenones, organoleptic uses thereof and process for preparing same | INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) | 1983-08-23 | — | — | US | claimed |
| EP-0027948-A1 | Tetrahydro-fluorene compounds, processes for their preparation and pharmaceutical compositions thereof | MERCK & CO. INC. (US) | 1981-05-06 | — | — | EP | claimed |