SCHEMBL138979

SCHEMBL138979

N[C@H]1CC[C@H](N2CCOCC2)CC1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.44
L3MBTL3 Q96JM7 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
KDM1A O60341 1/20 0.38
MAOB P27338 1/20 0.38
OPRL1 P41146 2/20 0.38
ALDH1A1 P00352 3/20 0.35
CYP2A13 Q16696 1/20 0.35
HPGD P15428 1/20 0.35
IRAK4 Q9NWZ3 4/20 0.35
IRAK2 O43187 1/20 0.35
CLK1 P49759 1/20 0.35
CLK2 P49760 1/20 0.35
IRAK1 P51617 1/20 0.35
HASPIN Q8TF76 1/20 0.35
CLK4 Q9HAZ1 1/20 0.35
IRAK3 Q9Y616 1/20 0.35
HRH3 Q9Y5N1 4/20 0.34
CYP3A4 P08684 1/20 0.33
CYP2C9 P11712 1/20 0.33

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
SCHEMBL138980 1.00 SMN1; SMN2 (0.44) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL862083 1.00 SMN1; SMN2 (0.44) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
Hydrochloric Acid SCHEMBL1699971 0.98 SMN1; SMN2 (0.42) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
Hydrochloric Acid SCHEMBL15227231 0.98 SMN1; SMN2 (0.42) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
Hydrochloric Acid SCHEMBL16593368 0.98 SMN1; SMN2 (0.42) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
Hydrochloric Acid SCHEMBL1699970 0.98 SMN1; SMN2 (0.42) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL15134619 0.88 HRH3 (0.44) SMN1; SMN2HRH3
SCHEMBL3168997 0.87
SCHEMBL26112782 0.87 SMN1; SMN2 (0.52) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB
SCHEMBL26112778 0.87 SMN1; SMN2 (0.52) SMN1; SMN2L3MBTL3L3MBTL1KDM1AMAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12378250-B2 Tricyclic compound as IRAK4 inhibitor KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2025-08-05 US disclosed
US-20250145625-A1 PYRAZOLOPYRIMIDINE DERIVATIVE AND ANTICANCER PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2025-05-08 US disclosed
CN-119841829-A Compounds for the treatment of PI3K gamma mediated diseases and uses thereof 中国科学院合肥物质科学研究院 2025-04-18 CN disclosed
EP-3885348-B1 NOVEL TRICYCLIC COMPOUND AS IRAK4 INHIBITOR KOREA RES INST CHEMICAL TECH (KR) 2025-02-12 EP disclosed
EP-4458827-A1 PYRAZOLOPYRIMIDINE DERIVATIVE AND ANTICANCER PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT Korea Research Institute of Chemical Technology (KR) 2024-11-06 EP disclosed
CN-118894861-A Novel tricyclic compounds as IRAK4 inhibitors 韩国化学研究院 2024-11-05 CN disclosed
CN-118414337-A Pyrazolopyrimidine derivative and anticancer pharmaceutical composition containing same as active ingredient 韩国化学研究院 2024-07-30 CN disclosed
CN-113227095-B Novel tricyclic compounds as IRAK4 inhibitors 韩国化学研究院 2024-07-05 CN disclosed
WO-2024068740-A1 NOVEL CDK9 INHIBITORS ORIGENIS GMBH (DE) 2024-04-04 WO disclosed
EP-3560499-B1 DIHYDROPTERIDINONES FOR THE TREATMENT OF CANCER DISEASES ONCOHEROES BIOSCIENCES INC (US) 2024-03-06 EP disclosed
US-20060009457-A1 New pyridodihydropyrazinones, process for their manufacture and use thereof as medicaments BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2006-01-12 US disclosed
EP-1599478-A1 DIHYDROPTERIDINONES, METHOD FOR THE PRODUCTION AND USE THEREOF IN THE FORM OF DRUGS Boehringer Ingelheim Pharma GmbH & Co.KG (DE) 2005-11-30 EP disclosed
US-20050261295-A1 2-Anilino-4-amino-, -oxy- or -thio-substituted, e.g., 2-(2-methoxy-4-N-propylcarbamoyl-phenylamino)-4-(2-carboxy-3-fluoro-phenylamino)-5-trifluoromethyl-pyrimidine; and 3-anilino--5-amino-, -oxy- or -thio-substituted 1,2,4-triazines; antiproliferative agents BOEHRINGER INGELHEIM INTERNATIONAL GMBH (DE) 2005-11-24 US disclosed
EP-1598343-A1 2-Arylaminopyrimidine derivatives as PLK inhibitors Boehringer Ingelheim International GmbH (DE) 2005-11-23 EP disclosed
WO-2005105790-A1 4- 2- (CYCLOALKYLAMINO) PYRIMIDIN-4-YL ! - (PHENYL) - IMIDAZOLIN-2- ONE DERIVATIVES AS P38 MAP- KINASE INHIBITORS FOR THE TREATMENT OF INFLAMMATORY DISEASES TANABE SEIYAKU CO., LTD. (JP) 2005-11-10 WO disclosed
US-6861422-B2 Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-03-01 US disclosed
US-20050014761-A1 Intermediate compounds for making dihydropteridinones useful as pharmaceutical compositions BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG 2005-01-20 US disclosed
US-20050014760-A1 Methods of treating diseases or conditions using dihydropteridinone compounds BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG (DE) 2005-01-20 US disclosed
WO-2004076454-A1 DIHYDROPTERIDINONES, METHOD FOR THE PRODUCTION AND USE THEREOF IN THE FORM OF DRUGS BOEHRINGER INGELHEIM PHARMA GMBH & CO KG (DE) 2004-09-10 WO disclosed
US-20040176380-A1 New dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions BOEHRINGER INGELHEIM PHARMA GMBH CO. KG (DE) 2004-09-09 US 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 (7 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-20060009457-A1 New pyridodihydropyrazinones, process for their manufacture and use thereof as medicaments PLPBP, CYP2D6, CYP2B6 SMN1; SMN2 4669/4885L3MBTL3 4398/4885L3MBTL1 4304/4885
US-20250145625-A1 PYRAZOLOPYRIMIDINE DERIVATIVE AND ANTICANCER PHARMACEUTICAL COMPOSITION CONTAINING SAME AS ACTIVE INGREDIENT DPYD, TP53, WASHC5 SMN1; SMN2 3352/4885L3MBTL3 4871/4885L3MBTL1 4872/4885
US-20050261295-A1 2-Anilino-4-amino-, -oxy- or -thio-substituted, e.g., 2-(2-methoxy-4-N-propylcarbamoyl-phenylamino)-4-(2-carboxy-3-fluoro-phenylamino)-5-trifluoromethyl-pyrimidine; and 3-anilino--5-amino-, -oxy- or -thio-substituted 1,2,4-triazines; antiproliferative agents MKI67, CCNY, CCNO SMN1; SMN2 2193/4885L3MBTL3 1831/4885L3MBTL1 1594/4885
US-20040176380-A1 New dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions QDPR, DHPS, DRD5 SMN1; SMN2 4582/4885L3MBTL3 4854/4885L3MBTL1 4487/4885
US-12378250-B2 Tricyclic compound as IRAK4 inhibitor IRAK4, IRAK1, IRAK2 SMN1; SMN2 2401/4885L3MBTL3 3661/4885L3MBTL1 1925/4885
US-20050014760-A1 Methods of treating diseases or conditions using dihydropteridinone compounds QDPR, DHPS, DHFR SMN1; SMN2 1711/4885L3MBTL3 1941/4885L3MBTL1 1277/4885
US-20050014761-A1 Intermediate compounds for making dihydropteridinones useful as pharmaceutical compositions QDPR, DHPS, DHODH SMN1; SMN2 4436/4885L3MBTL3 3917/4885L3MBTL1 3166/4885

“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.