SCHEMBL2019492

SCHEMBL2019492

CC1(C)CC(=O)C(C)(C)N1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.46
ALDH1A1 P00352 4/20 0.37
HTT P42858 4/20 0.35
LMNA P02545 2/20 0.35
MAPT P10636 1/20 0.35
CYP2C19 P33261 3/20 0.32
KDM4E B2RXH2 2/20 0.32
TSHR P16473 2/20 0.32
CYP1A2 P05177 1/20 0.32
HPGD P15428 1/20 0.32
CDK5 Q00535 1/20 0.32
CDK5R1 Q15078 1/20 0.32
NCOA1 Q15788 1/20 0.32
NCOA3 Q9Y6Q9 1/20 0.32
MEN1 O00255 1/20 0.31
MAPK1 P28482 1/20 0.31
KMT2A Q03164 1/20 0.31
CYP3A4 P08684 1/20 0.30
CYP2D6 P10635 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30

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.

Compoundsimilaritytop predictedshared targets
SCHEMBL9847498 0.75 SMN1; SMN2 (0.31) SMN1; SMN2
SCHEMBL2493319 0.74 SMN1; SMN2 (0.33) SMN1; SMN2
SCHEMBL5243332 0.74 SMN1; SMN2 (0.43) SMN1; SMN2ALDH1A1HTTLMNAMAPT
Hydrochloric Acid SCHEMBL7688487 0.72 SMN1; SMN2 (0.32) SMN1; SMN2
SCHEMBL38953 0.71 SMN1; SMN2 (0.56) SMN1; SMN2ALDH1A1HTTLMNACYP2C19
Water SCHEMBL4837114 0.69 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1LMNACYP2C19KDM4E
Iodide SCHEMBL11830139 0.69 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1LMNACYP2C19KDM4E
Hydrochloric Acid SCHEMBL20704047 0.69 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1LMNACYP2C19KDM4E
Water SCHEMBL7733637 0.69 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1LMNACYP2C19KDM4E
SCHEMBL29829697 0.69 SMN1; SMN2 (0.54) SMN1; SMN2ALDH1A1LMNACYP2C19KDM4E

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 152 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0035889-B1 ALKYL-METAL COCATALYST EXXON RESEARCH AND ENGINEERING COMPANY (US) 1984-05-02 EP claimed
EP-4568764-B1 INTEGRATION OF A HEAT PUMP CIRCUIT INTO A DISTILLATION PLANT FOR POLYMERIZABLE SUBSTANCES BASF SE (DE) 2026-04-29 EP disclosed
EP-4543865-B1 PROCESS FOR PREPARING SOLKETAL ACRYLATE BY TRANSESTERIFICATION BASF SE (DE) 2026-04-29 EP disclosed
US-20260008742-A1 CONTINUOUS PROCESS FOR PRODUCING N-BUTYL (METH)ACRYLATE WITH A CATALYST RECIRCULATION SYSTEM BASF SE (DE) 2026-01-08 US disclosed
WO-2025261823-A1 PROCESS FOR MANUFACTURE OF (METH)ACRYLATES BASF SE (DE) 2025-12-26 WO disclosed
US-20250282705-A1 PREPARATION OF TERMINALLY UNSATURATED (METH)ACRYLATE CROSSLINKERS RÖHM GMBH (DE) 2025-09-11 US disclosed
EP-4613785-A1 ESTER-COMPOUND-CONTAINING COMPOSITION AND METHOD FOR PRODUCING SAME, POLYMERIZABLE COMPOSITION, AND (METH)ACRYLIC POLYMER AND METHOD FOR PRODUCING SAME Mitsubishi Chemical Corporation (JP) 2025-09-10 EP disclosed
EP-4613784-A1 ESTER COMPOUND-CONTAINING COMPOSITION, METHOD FOR PRODUCING SAME, POLYMERIZABLE COMPOSITION, (METH)ACRYLIC POLYMER, AND METHOD FOR PRODUCING SAME Mitsubishi Chemical Corporation (JP) 2025-09-10 EP disclosed
EP-4610284-A1 MONOMER COMPOSITION, METHACRYLIC RESIN COMPOSITION AND PRODUCTION METHOD THEREFOR, AND MOLDED RESIN OBJECT Mitsubishi Chemical Corporation (JP) 2025-09-03 EP disclosed
EP-4419580-B1 METHOD FOR PROMOTING HYDROSILYLATION REACTION TO PREPARE ESTER-FUNCTIONAL SILOXANE OLIGOMERS DOW GLOBAL TECHNOLOGIES LLC (US) 2025-08-27 EP disclosed
CN-1202050-C Polymerization inhibiting method for ethenyl chemical compound NIPPON CATALYTIC CHEM IND (JP) 2005-05-18 CN disclosed
US-20050077240-A1 Rectificative separation of an acrylic acid-containing liquid BASF AKTIENGESELLSCHAFT (DE) 2005-04-14 US disclosed
EP-1427692-A1 METHOD FOR PRODUCING (METH)ACRYLIC ACID ESTERS BASF AKTIENGESELLSCHAFT (DE) 2004-06-16 EP disclosed
US-20040031674-A1 Workup of (meth)acrylic acid and (meth)acrylic esters BASF AKIENGESELLSCHAFT (DE) 2004-02-19 US disclosed
WO-2003022793-A1 METHOD FOR PRODUCING (METH)ACRYLIC ACID ESTERS BASF AKTIENGESELLSCHAFT (DE) 2003-03-20 WO disclosed
CN-1243115-A Polymerization inhibiting method for ethenyl chemical compound NIPPON CATALYTIC CHEM IND (JP) 2000-02-02 CN disclosed
US-5583188-A USING TITANIUM, ORGANOALUMINUM, NITROGEN OR OXYGEN HETEROCYCLE CONTAINING CATALYST MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1996-12-10 US disclosed
US-4678767-A COORDINATION CATALYST YIELDING POLYMERS OF HIGH BULK DENSITY TOA NENRYO KOGYO KABUSHIKI KAISHA (JP) 1987-07-07 US disclosed
EP-0086644-B1 CATALYST COMPOSITION AND PROCESS FOR POLYMERIZING OLEFINS MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1987-05-06 EP disclosed
EP-0086644-A2 Catalyst composition and process for polymerizing olefins MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1983-08-24 EP 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 (2 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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250282705-A1 PREPARATION OF TERMINALLY UNSATURATED (METH)ACRYLATE CROSSLINKERS MTHFD2, MMAB, PAM SMN1; SMN2 3657/4885ALDH1A1 153/4885HTT 51/4885
US-20260008742-A1 CONTINUOUS PROCESS FOR PRODUCING N-BUTYL (METH)ACRYLATE WITH A CATALYST RECIRCULATION SYSTEM MMAB, ALKBH1, ALKBH3 SMN1; SMN2 806/4885ALDH1A1 134/4885HTT 2033/4885

“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.