Known targets — ChEMBL curated mechanism
MMP1MMP13MMP7MMP8polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO
The experimentally established mechanism targets of Piperidine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.
⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.
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 | |
|---|---|---|---|---|
| Piperidine SCHEMBL27734261 | 0.97 | ALDH1A1 (0.56) | — | |
| Piperidine SCHEMBL6836703 | 0.97 | ALDH1A1 (0.56) | — | |
| Piperidine SCHEMBL28352932 | 0.97 | ALDH1A1 (0.56) | — | |
| Pyrrolidine SCHEMBL5683314 | 0.97 | ALDH1A1 (0.53) | — | |
| Pyrrolidine SCHEMBL222328 | 0.97 | — | — | |
| Cyclohexane SCHEMBL28639868 | 0.90 | ALDH1A1 (0.44) | — | |
| Azetidine SCHEMBL22833205 | 0.89 | ALDH1A1 (0.50) | — | |
| Azetidine SCHEMBL1500479 | 0.89 | — | — | |
| Piperidine SCHEMBL28006849 | 0.89 | ALDH1A1 (0.47) | — | |
| Piperidine SCHEMBL2914572 | 0.88 | ALDH1A1 (0.53) | — |
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 2411 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-4607278-A1 | CHEMICALLY-AMPLIFIED POSITIVE PHOTORESIST COMPOSITION FOR PATTERN PROFILE IMPROVEMENT AND ETCH RESISTANCE ENHANCEMENT | Ycchem Co., Ltd. (KR) | 2025-08-27 | — | — | EP | claimed |
| US-20250229219-A1 | CARBON DIOXIDE CAPTURE AGENT CONTAINING TWO TYPES OF AMINE COMPOUNDS AND CARBON DIOXIDE CAPTURE METHOD USING THE SAME | KOREA INSTITUTE OF ENERGY RESEARCH (KR) | 2025-07-17 | — | — | US | claimed |
| US-20250199405-A1 | CHEMICALLY-AMPLIFIED POSITIVE PHOTORESIST COMPOSITION FOR PATTERN PROFILE IMPROVEMENT AND ETCH RESISTANCE ENHANCEMENT | YCCHEM CO., LTD. (KR) | 2025-06-19 | — | — | US | claimed |
| US-12286453-B2 | Methods of sequencing using nucleotides with 3′ acetal blocking group | ILLUMINA CAMBRIDGE LIMITED (GB) | 2025-04-29 | — | — | US | claimed |
| US-20240209015-A1 | METHODS OF SEQUENCING USING 3' BLOCKED NUCLEOTIDES | ILLUMINA, INC. | 2024-06-27 | — | — | US | claimed |
| CN-116083514-B | Pig bird tie-in additive and screening method thereof | 青岛农业大学 | 2024-06-25 | — | — | CN | claimed |
| EP-3154937-B1 | CHLORINE-RESISTANT POLYETHYLENE COMPOUND AND ARTICLES MADE THEREFROM | FINA TECHNOLOGY (US) | 2024-05-22 | — | — | EP | claimed |
| WO-2024085293-A1 | CHEMICALLY-AMPLIFIED POSITIVE PHOTORESIST COMPOSITION FOR PATTERN PROFILE IMPROVEMENT AND ETCH RESISTANCE ENHANCEMENT | 영창케미칼 주식회사 | 2024-04-25 | — | — | WO | claimed |
| US-20240132532-A1 | METHODS OF SEQUENCING USING NUCLEOTIDES WITH 3' ACETAL BLOCKING GROUP | ILLUMINA CAMBRIDGE LIMITED (GB) | 2024-04-25 | — | — | US | claimed |
| US-11873568-B2 | Compositions and methods for the electrodeposition of nanotwinned copper | MACDERMID ENTHONE INC. (US) | 2024-01-16 | — | — | US | claimed |
| EP-0219332-A2 | Tartrate compounds useful as light stabilizers for plastics | ICI AMERICAS INC. (US) | 1987-04-22 | — | — | EP | claimed |
| US-4546177-A | 1-(6-Hydroxy-4- or -7-methoxy-5-Benzofuranyl)-4-substituted-1,3-butanediones | THE UPJOHN COMPANY (US) | 1985-10-08 | — | — | US | claimed |
| US-4434295-A | Anti-atherosclerotic 6,7-dihydro-7,7-disubstituted-khellin analogs | THE UPJOHN COMPANY (US) | 1984-02-28 | — | — | US | claimed |
| US-4240923-A | STERICALLY HINDERED AMINO ALCOHOLS INCLUDING HETEROCYCLIC PIPERIDINE COMPOUNDS | EXXON RESEARCH & ENGINEERING CO. (US) | 1980-12-23 | — | — | US | claimed |
| US-4240922-A | STERICALLY HINDERED AMINES INCLUDING HETEROCYCLIC COMPOUNDS AND TERTIARY AMINO ALCOHOLS INCREASE CARBON DIOXIDE ABSORBANCE | EXXON RESEARCH & ENGINEERING CO. (US) | 1980-12-23 | — | — | US | claimed |
| US-4217237-A | Process for removing carbon dioxide containing acidic gases from gaseous mixtures using a basic salt activated with a hindered amine | EXXON RESEARCH & ENGINEERING CO. (US) | 1980-08-12 | — | — | US | claimed |
| US-4112051-A | Process and amine-solvent absorbent for removing acidic gases from gaseous mixtures | EXXON RESEARCH & ENGINEERING CO. (US) | 1978-09-05 | — | — | US | claimed |
| US-4112052-A | Process for removing carbon dioxide containing acidic gases from gaseous mixtures using aqueous amine scrubbing solutions | EXXON RESEARCH & ENGINEERING CO. (US) | 1978-09-05 | — | — | US | claimed |
| US-4112050-A | Process for removing carbon dioxide containing acidic gases from gaseous mixtures using a basic salt activated with a hindered amine | EXXON RESEARCH & ENGINEERING CO. (US) | 1978-09-05 | — | — | US | claimed |
| US-4100257-A | Process and amine-solvent absorbent for removing acidic gases from gaseous mixtures | EXXON RESEARCH & ENGINEERING CO. (US) | 1978-07-11 | — | — | US | claimed |