SCHEMBL2184100

SCHEMBL2184100

CCC(CC)(CC)C(C)N

nearest known ligand 0.33

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.33
OPRM1 P35372 1/20 0.30
TSHR P16473 1/20 0.30
MAPK1 P28482 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
SCHEMBL349071 0.82 DPP4 (0.32)
SCHEMBL29160444 0.80 ALDH1A1 (0.32) ALDH1A1
SCHEMBL12884373 0.71 ALDH1A1 (0.33) ALDH1A1OPRM1TSHRMAPK1
Water SCHEMBL18549326 0.71 OPRM1 (0.32) OPRM1
SCHEMBL9713104 0.69 TSHR (0.33) TSHR
SCHEMBL28731475 0.69 TSHR (0.30) TSHR
SCHEMBL23096948 0.69
SCHEMBL4659025 0.69
SCHEMBL1352336 0.69 TDP1 (0.39) ALDH1A1TSHRMAPK1
SCHEMBL31153121 0.69

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 49 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-20070144970-A1 Supported zeolite membranes, their process for production and their applications INSTITUT FRANCAIS DU PETROLE (FR) 2007-06-28 US 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
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
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-2023134629-A1 NUCLEAR TRANSPORT REGULATOR AND USE THEREOF 上海海雁医药科技有限公司 2023-07-20 WO disclosed
WO-2022257960-A1 BICYCLIC COMPOUND FOR THE TREATMENT OF EP2 AND EP4 RECEPTOR-MEDIATED DISEASES 武汉人福创新药物研发中心有限公司 2022-12-15 WO disclosed
US-7125997-B2 Differential tumor cytotoxicity compounds and compositions IRM LLC (BM) 2006-10-24 US disclosed
US-7115651-B2 Macrocycles and uses thereof SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2006-10-03 US disclosed
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 disclosed
WO-2005061481-A1 NOVEL MA CROCYCLES AND USES THEREOF SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 2005-07-07 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-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 ALDH1A1 205/4885OPRM1 1600/4885TSHR 4210/4885
US-20070043093-A1 Glucagon-like peptide-1 receptor agonists, the preparation and the use of the same GLP1R, GCGR, GIPR ALDH1A1 4201/4885OPRM1 1100/4885TSHR 48/4885
US-20260015341-A1 PI3K INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF PIK3CA, PIK3R4, PIK3R1 ALDH1A1 2781/4885OPRM1 3017/4885TSHR 1648/4885
US-20240368203-A1 DEGRADATION OF (EGFR) BY CONJUGATION OF EGFR INHIBITORS WITH E3 LIGASE LIGAND AND METHODS OF USE EGFR, CBL, ERBB2 ALDH1A1 3281/4885OPRM1 3695/4885TSHR 2105/4885

“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.