SCHEMBL676894

SCHEMBL676894

c1cnc(C2CCCC2)nc1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 3/20 0.43
GAA P10253 1/20 0.43
CYP11B2 P19099 1/20 0.40
POLB P06746 1/20 0.37
CASP3 P42574 1/20 0.37
SENP7 Q9BQF6 1/20 0.37
SENP6 Q9GZR1 1/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
MAPK1 P28482 2/20 0.37
ALDH1A1 P00352 2/20 0.37
NPC1 O15118 1/20 0.37
TP53 P04637 1/20 0.37
RAB9A P51151 1/20 0.37
CYP1A2 P05177 1/20 0.35
GRM5 P41594 1/20 0.35
OPRL1 P41146 3/20 0.35
OPRM1 P35372 1/20 0.35
L3MBTL1 Q9Y468 2/20 0.34
KMT2A Q03164 2/20 0.34
GLA P06280 1/20 0.34

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
SCHEMBL16916365 0.97 KDM4E (0.46) KDM4EGAACYP11B2POLBCASP3
SCHEMBL61212 0.97 KDM4E (0.46) KDM4EGAACYP11B2POLBCASP3
Ammonia Solution, Strong SCHEMBL28326987 0.97 KDM4E (0.41) KDM4EGAACYP11B2POLBCASP3
SCHEMBL1444138 0.94 KDM4E (0.38) KDM4EGAACYP11B2POLBCASP3
SCHEMBL935722 0.88
Hydrochloric Acid SCHEMBL29162507 0.86 OPRL1 (0.36) KDM4EGAAMAPK1OPRL1OPRM1
Carbamic Acid SCHEMBL9705391 0.83 KDM4E (0.45) KDM4EGAACYP11B2POLBCASP3
Fluoromethane SCHEMBL28832696 0.81 PDE10A (0.34) KDM4EGAAMAPK1OPRL1OPRM1
SCHEMBL2103674 0.79 OPRM1 (0.33) KDM4EGAAOPRL1OPRM1
SCHEMBL12539825 0.77 MAPK1 (0.50) MAPK1OPRL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3125920-A2 USE OF DIANHYDROGALACTITOL AND ANALOGS OR DERIVATIVES THEREOF TO TREAT NON-SMALL-CELL CARCINOMA OF THE LUNG AND OVARIAN CANCER Del Mar Pharmaceuticals (CA) 2017-02-08 EP claimed
CN-105198864-A Solvent-free preparation method of cyclopentyl pyrimidine compound HUAREN PHARMACEUTICAL CO LTD 2015-12-30 CN claimed
WO-2015154064-A2 USE OF DIANHYDROGALACTITOL AND ANALOGS OR DERIVATIVES THEREOF TO TREAT NON-SMALL-CELL CARCINOMA OF THE LUNG AND OVARIAN CANCER DEL MAR PHARMACEUTICALS (CA) 2015-10-08 WO claimed
CN-112898210-B Process for preparing pyrimidinylcyclopentane compounds 豪夫迈·罗氏有限公司 2025-02-21 CN disclosed
CN-112898210-B Process for preparing pyrimidinylcyclopentane compounds 豪夫迈·罗氏有限公司 2025-02-21 CN disclosed
US-12202826-B2 N-pyridinyl acetamide derivatives as inhibitors of the Wnt signaling pathway REDX PHARMA PLC (GB) 2025-01-21 US disclosed
EP-4282973-A3 PROCESSES FOR THE PREPARATION OF PYRIMIDINYLCYCLOPENTANE COMPOUNDS F. Hoffmann-La Roche AG (CH) 2024-03-27 EP disclosed
US-11840539-B2 Substituted pyrrolo,-furano, and cyclopentylpyrimidines having antimitotic and/or antitumor activity and methods of use thereof DUQUESNE UNIVERSITY OF THE HOLY SPIRIT (US) 2023-12-12 US disclosed
US-11840539-B2 Substituted pyrrolo,-furano, and cyclopentylpyrimidines having antimitotic and/or antitumor activity and methods of use thereof DUQUESNE UNIVERSITY OF THE HOLY SPIRIT (US) 2023-12-12 US disclosed
EP-4282973-A2 PROCESSES FOR THE PREPARATION OF PYRIMIDINYLCYCLOPENTANE COMPOUNDS F. Hoffmann-La Roche AG (CH) 2023-11-29 EP disclosed
EP-4282973-A2 PROCESSES FOR THE PREPARATION OF PYRIMIDINYLCYCLOPENTANE COMPOUNDS F. Hoffmann-La Roche AG (CH) 2023-11-29 EP disclosed
EP-2404907-A1 Pyrimidyl cyclopentanes as AKT protein kinase inhibitors Array Biopharma, Inc. (US) 2012-01-11 EP disclosed
US-8063050-B2 Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors ARRAY BIOPHARMA INC. (US) 2011-11-22 US disclosed
CN-102015708-A Pyrimidyl cyclopentanes as AKT protein kinase inhibitors ARRAY BIOPHARMA INC 2011-04-13 CN disclosed
CN-101932564-A Hydroxylated pyrimidyl cyclopentanes as the AKT kinases inhibitor ARRAY BIOPHARMA INC 2010-12-29 CN disclosed
CN-101932565-A Hydroxylated pyrimidyl cyclopentane as the AKT kinases inhibitor GENENTECH INC 2010-12-29 CN disclosed
CN-101932565-A Hydroxylated pyrimidyl cyclopentane as the AKT kinases inhibitor GENENTECH INC 2010-12-29 CN disclosed
CN-101932564-A Hydroxylated pyrimidyl cyclopentanes as the AKT kinases inhibitor ARRAY BIOPHARMA INC 2010-12-29 CN disclosed
US-20100233733-A1 MULTIPLE MECHANISMS FOR MODULATION OF THE PI3 KINASE PATHWAY NODALITY, INC., A DELAWARE CORPORATION (US) 2010-09-16 US disclosed
US-20100035863-A1 2 Amino-Pyrimidine Derivatives As H4 Receptor Antagonists, Processes For Preparing Them And Their Use In Pharmaceutical Compositions UCB PHARMA, S.A. (BE) 2010-02-11 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 (3 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-12202826-B2 N-pyridinyl acetamide derivatives as inhibitors of the Wnt signaling pathway WNT1, WNT3, CTNNB1 KDM4E 1635/4885GAA 3180/4885CYP11B2 1433/4885
US-11840539-B2 Substituted pyrrolo,-furano, and cyclopentylpyrimidines having antimitotic and/or antitumor activity and methods of use thereof ABCB1, ABCC1, ABCG2 KDM4E 1977/4885GAA 1307/4885CYP11B2 1779/4885
US-20100035863-A1 2 Amino-Pyrimidine Derivatives As H4 Receptor Antagonists, Processes For Preparing Them And Their Use In Pharmaceutical Compositions HRH4, HRH2, HRH3 KDM4E 1873/4885GAA 4116/4885CYP11B2 1778/4885

“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.