SCHEMBL2184102

SCHEMBL2184102

CCCN(CC)C(C)CC

nearest known ligand 0.37

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
FDPS P14324 1/20 0.37
CYP2D6 P10635 1/20 0.35
KCNE1 P15382 1/20 0.35
KCNA5 P22460 1/20 0.35

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
SCHEMBL172247 0.88 FDPS (0.40) FDPSKCNA5
SCHEMBL13452916 0.88 FDPS (0.40) FDPSKCNA5
SCHEMBL7770538 0.87 CA12 (0.31)
Water SCHEMBL27796806 0.85 FDPS (0.39) FDPSKCNA5
Hydrochloric Acid SCHEMBL22575642 0.85 FDPS (0.39) FDPSKCNA5
SCHEMBL15579409 0.85 DNM1 (0.39)
SCHEMBL193496 0.84
SCHEMBL13452838 0.84
SCHEMBL19889381 0.83 FDPS (0.34) FDPSCYP2D6KCNE1KCNA5
Hydrochloric Acid SCHEMBL22575404 0.81 KDM4E (0.34) FDPSCYP2D6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101443330-A Heterocyclic non-nucleoside compound, preparation method thereof, pharmaceutical composition and application thereof as antiviral inhibitor SHANGHAI INST MATERIA MEDICA (CN) 2009-05-27 CN claimed
EP-2030974-A1 HETEROCYCLIC NON-NUCLEOSIDE COMPOUNDS, THEIR PEPARATION, PHARMACEUTICAL COMPOSITION AND THEIR USE AS ANTIVIRAL AGENTS Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CN) 2009-03-04 EP claimed
US-20070043093-A1 Glucagon-like peptide-1 receptor agonists, the preparation and the use of the same SHANGHAI INSTITUTE OF MATERIA MEDICA, CHINESE ACADEMY OF SCIENCES (CN) 2007-02-22 US claimed
EP-1695968-A1 THE GLUCAGON-LIKE PEPTIDE-1 RECEPTOR AGONISTS, THE PREPARATION AND THE USE OF THE SAME Shanghai Institute of Materia Medica, Chinese Academy of Sciences (CN) 2006-08-30 EP claimed
US-20260015341-A1 PI3K INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF HINOVA PHARMACEUTICALS INC (CN) 2026-01-15 US disclosed
EP-4553075-A1 PI3K INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF Hinova Pharmaceuticals Inc. (CN) 2025-05-14 EP disclosed
CN-119176786-A Double chiral center thiazolidineone derivative and preparation method and application thereof 上海体育大学 2024-12-24 CN disclosed
US-20240368203-A1 DEGRADATION OF (EGFR) BY CONJUGATION OF EGFR INHIBITORS WITH E3 LIGASE LIGAND AND METHODS OF USE BEIGENE, LTD. (KY) 2024-11-07 US disclosed
CN-118843613-A RXFP1 agonists 百时美施贵宝公司 2024-10-25 CN disclosed
CN-113444086-B Ezh2 inhibitors and uses thereof 达纳-法伯癌症研究所股份有限公司 2024-04-30 CN disclosed
WO-2024008122-A1 PI3K INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF 海创药业股份有限公司 2024-01-11 WO disclosed
CN-117362281-A PI3K inhibitor and preparation method and application thereof 海创药业股份有限公司 2024-01-09 CN disclosed
WO-2005032468-A2 MONOCYCLIC AND BICYCLIC LACTAMS AS FACTOR XA INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-04-14 WO disclosed
WO-2004058713-A1 DIFFERENTIAL TUMOR CYTOTOXOCITY COMPOUNDS AND COMPOSITIONS IRM LLC (BM) 2004-07-15 WO disclosed
US-20040132786-A1 Differential tumor cytotoxicity compounds and compositions IRM LLC, A DELAWARE LIMITED LIABILITY COMPANY (BM) 2004-07-08 US disclosed
EP-0838508-B1 Aqueous ink composition for use in an ink-jet printer SEIKO EPSON CORP (JP) 2001-08-29 EP disclosed
US-5871572-A COLORANT, WATER, A WATER-SOLUBLE ORGANIC SOLVENT, AND PECTIC ACID SEIKO EPSON CORPORATION (JP) 1999-02-16 US disclosed
EP-0838508-A2 Aqueous ink composition for use in an ink-jet printer SEIKO EPSON CORPORATION (JP) 1998-04-29 EP disclosed
EP-0177933-B1 INTERMEDIATES FOR MAKING 16-PHENOXY AND 16-SUBSTITUTED PHENOXY-PROSTATRIENOIC ACID DERIVATIVES SYNTEX (U.S.A.) INC. (US) 1989-05-10 EP disclosed
EP-0177933-A2 Intermediates for making 16-phenoxy and 16-substituted phenoxy-prostatrienoic acid derivatives SYNTEX (U.S.A.) INC. (US) 1986-04-16 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 (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.

PatentTitleText reads most aboutPredicted target · text-rank
US-20040132786-A1 Differential tumor cytotoxicity compounds and compositions MIF, FOXM1, MYADM FDPS 2504/4885CYP2D6 3064/4885KCNE1 4717/4885
US-20070043093-A1 Glucagon-like peptide-1 receptor agonists, the preparation and the use of the same GLP1R, GCGR, GIPR FDPS 2850/4885CYP2D6 3788/4885KCNE1 2130/4885
US-20260015341-A1 PI3K INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF PIK3CA, PIK3R4, PIK3R1 FDPS 1026/4885CYP2D6 888/4885KCNE1 2981/4885
US-20240368203-A1 DEGRADATION OF (EGFR) BY CONJUGATION OF EGFR INHIBITORS WITH E3 LIGASE LIGAND AND METHODS OF USE EGFR, CBL, ERBB2 FDPS 4346/4885CYP2D6 4546/4885KCNE1 4558/4885

“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.