⚠ 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 | |
|---|---|---|---|---|
| Trifluoromethanesulfonic Acid SCHEMBL8352480 | 1.00 | ALDH1A1 (0.47) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL17510194 | 1.00 | ALDH1A1 (0.47) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL7027061 | 1.00 | ALDH1A1 (0.47) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL6086975 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL336134 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL7200669 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL15569457 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL15299906 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL15569456 | 0.96 | ALDH1A1 (0.45) | — | |
| Trifluoromethanesulfonic Acid SCHEMBL39465 | 0.96 | 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
Appears in 3820 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 |
|---|---|---|---|---|---|---|---|
| CN-117440957-B | Process for the production of biotin intermediates | DSM IP ASSETS B.V. (NL) | 2026-05-26 | — | — | CN | claimed |
| CN-122079748-A | Guaazulene triarylmethane, synthesis method and application thereof in preparation of antibacterial products | — | 2026-05-26 | — | — | CN | claimed |
| CN-122036496-A | Preparation method for co-production of acetyl chloride and phosphorous acid, and product and application thereof | 南通江山农药化工股份有限公司 | 2026-05-15 | — | — | CN | claimed |
| CN-122010956-A | Chiral 1, 4-diazabicyclo [3.1.1] heptane derivatives, synthesis and application thereof | 浙江师范大学 | 2026-05-12 | — | — | CN | claimed |
| US-20260090547-A1 | BIO-INSECTICIDES FROM WASTE BIOMASS | UNIVERSITY OF DELAWARE (US) | 2026-04-02 | — | — | US | claimed |
| EP-4709483-A1 | NEW 5H-PYRROLO[3,2-B:5,4-C']DIPYRIDINE DERIVATIVES AND 6,7,8,9-TETRAHYDRO-5H-PYRROLO[3,2-B:5,4-C']DIPYRIDINE USEFUL IN THE TREATMENT OF CANCER | Institut Regional du Cancer de Montpellier (FR) | 2026-03-18 | — | — | EP | claimed |
| US-20250368599-A1 | PROCESS FOR THE PREPARATION OF CYCLOHOMOGERANATES | BASF SE (DE) | 2025-12-04 | — | — | US | claimed |
| US-20250207001-A1 | Method of underwater bonding | HENKEL AG & CO KGAA (DE) | 2025-06-26 | — | — | US | claimed |
| CN-120118480-A | Degradable epoxy resin composite material with adjustable curing speed and preparation and moderate full recycling methods thereof | 哈尔滨工业大学 | 2025-06-10 | — | — | CN | claimed |
| EP-3898573-B1 | METHOD FOR MAKING A DI(AMINOARYL)FLUORENE COMPOUND | CYTEC IND INC (US) | 2025-05-28 | — | — | EP | claimed |
| EP-1155023-A1 | CHELATING COMPOUNDS AND THEIR COMPLEXES WITH PARAMAGNETIC METALS | BRACCO S.p.A. (IT) | 2001-11-21 | — | — | EP | claimed |
| US-6274383-B1 | REACTING AN AMINO BOUND TO A SOLID SUPPORT WITH AN ISATOIC ANHYDRIDE TO FORM A 2-AMINOBENZAMIDE BOUND TO THE SUPPORT, AND THEN REACTING WITH ALDEHYDE USING A LEWIS ACID CATALYST TO FORM A 2,3-DIHYDRO-4(1H)-QUINAZOLINONE BOUND TO SUPPORT | SEPRACOR INC. | 2001-08-14 | — | — | US | claimed |
| EP-1115695-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(N+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | Monsanto Company (US) | 2001-07-18 | — | — | EP | claimed |
| WO-2001046207-A1 | CHELATING COMPOUNDS, THEIR COMPLEXES WITH PARAMAGNETIC METALS | BRACCO S.P.A. (IT) | 2001-06-28 | — | — | WO | claimed |
| WO-2000018724-A1 | (R)-CHIRAL HALOGENATED 1-SUBSTITUTEDAMINO-(n+1)-ALKANOLS USEFUL FOR INHIBITING CHOLESTERYL ESTER TRANSFER PROTEIN ACTIVITY | MONSANTO COMPANY (US) | 2000-04-06 | — | — | WO | claimed |
| EP-0742194-B1 | Process for the preparation of substituted phenols | RHONE POULENC NUTRITION ANIMAL (FR) | 1999-08-04 | — | — | EP | claimed |
| EP-0658552-B1 | Process for the preparation of alpha-tocopherol derivatives | EISAI CO LTD (JP) | 1999-03-31 | — | — | EP | claimed |
| US-5744617-A | ALKYLATION OF PHENOLS WITH BUTADIENE DERIVATIVE | RHONE-POULENC NUTRITION ANIMALE (FR) | 1998-04-28 | — | — | US | claimed |
| US-5532387-A | CYCLIZATION OF TRIMETHYLHYDROQUINONE AND AN ALKENYL ALCOHOL, REUSABLE CATALYST, IIIB FLUOROSULFONATE, NITRATE, SULFATE, OR FLUOROALKYLSULFONATE | EISAI CO., LTD. (JP) | 1996-07-02 | — | — | US | claimed |
| EP-0658552-A1 | Process for the preparation of alpha-tocopherol derivatives | Eisai Co., Ltd. (JP) | 1995-06-21 | — | — | EP | claimed |