SCHEMBL176995

SCHEMBL176995

O=C(O)CN1CCNC1=O

nearest known ligand 0.44

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
POLB P06746 4/20 0.44
KMT2A Q03164 4/20 0.44
CYP2C9 P11712 3/20 0.44
CYP2C19 P33261 3/20 0.44
CYP2D6 P10635 2/20 0.44
TSHR P16473 2/20 0.44
ALDH1A1 P00352 2/20 0.43
RET P07949 1/20 0.42
KDR P35968 1/20 0.42
ACE P12821 2/20 0.42
LMNA P02545 1/20 0.41
MAPT P10636 2/20 0.40
MEN1 O00255 2/20 0.40
RAB9A P51151 1/20 0.40
KDM4E B2RXH2 1/20 0.40
CYP1A2 P05177 1/20 0.40
CYP3A4 P08684 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.40

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
SCHEMBL8177700 0.82 CYP2D6 (0.41) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL8520401 0.81 POLB (0.42) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL3452808 0.81 TSHR (0.50) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL6877063 0.81 KMT2A (0.42) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL5590383 0.80 ALDH1A1 (0.39) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL8343320 0.79 KMT2A (0.47) POLBKMT2ACYP2C9CYP2C19CYP2D6
Cyclocreatine SCHEMBL450343 0.79 CYP2D6 (0.39) POLBKMT2ACYP2C9CYP2C19CYP2D6
Cyclocreatine SCHEMBL7935371 0.79 CYP2D6 (0.39) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL6070489 0.79 KMT2A (0.44) POLBKMT2ACYP2C9CYP2C19CYP2D6
SCHEMBL28931873 0.78 FAAH (0.51) POLBALDH1A1RETKDRMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250223266-A1 PARG INHIBITORY COMPOUNDS CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2025-07-10 US disclosed
EP-4522596-A1 DIHYDROINDENE DERIVATIVES AS MALT1 INHIBITORS C4X Discovery Limited (GB) 2025-03-19 EP disclosed
CN-119497712-A Indane derivatives as MALT1 inhibitors 希四克斯探索有限公司 2025-02-21 CN disclosed
US-12129236-B2 PARG inhibitory compounds CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2024-10-29 US disclosed
CN-112979631-B PARG inhibiting compounds 癌症研究科技有限公司 2024-09-20 CN disclosed
WO-2023218203-A1 DIHYDROINDENE DERIVATIVES AS MALT1 INHIBITORS C4X DISCOVERY LIMITED (GB) 2023-11-16 WO disclosed
US-20230136702-A1 Inhibitors of Human Herpesviruses THE GOVERNORS OF THE UNIVERSTIY OF ALBERTA (CA) 2023-05-04 US disclosed
US-20220340893-A1 BI-FUNCTIONAL COMPLEXES AND METHODS FOR MAKING AND USING SUCH COMPLEXES NUEVOLUTION A/S (DK) 2022-10-27 US disclosed
CN-114787114-A Improved process for the photocatalytic hydrocarboxylation of methanol using CO2 to produce acetic acid 科学和工业研究理事会是印度注册的机构(1860年第XXI号法案) 2022-07-22 CN disclosed
US-20210380539-A1 PARG INHIBITORY COMPOUNDS CANCER RESEARCH TECHNOLOGY LIMITED (GB) 2021-12-09 US disclosed
US-20100286191-A1 2-Arylthiazole Derivatives as CXCR3 Receptor Modulators MERCK SHARP & DOHME CORP. 2010-11-11 US disclosed
US-20100286191-A1 2-Arylthiazole Derivatives as CXCR3 Receptor Modulators MERCK SHARP & DOHME CORP. 2010-11-11 US disclosed
US-7790747-B2 Chemokine receptor binding compounds GENZYME CORPORATION (US) 2010-09-07 US disclosed
WO-2010043000-A1 S1P RECEPTORS MODULATORS AND THEIR USE THEREOF AKAAL PHARMA PTY LTD (AU) 2010-04-22 WO disclosed
EP-1942890-A4 CHEMOKINE RECEPTOR BINDING COMPOUNDS GENZYME CORP (US) 2009-08-26 EP disclosed
US-20090099205-A1 Chemokine receptor binding compounds GENZYME CORPORATION 2009-04-16 US disclosed
EP-1942890-A2 CHEMOKINE RECEPTOR BINDING COMPOUNDS ANORMED INC. (CA) 2008-07-16 EP disclosed
US-20080132500-A1 Antibiotic compounds MERCK SHARP & DOHME CORP. 2008-06-05 US disclosed
WO-2007070433-A2 2-ARYLTHIAZOLE DERIVATIVES AS CXCR3 RECEPTOR MODULATORS MERCK & CO., INC. (US) 2007-06-21 WO disclosed
WO-2006138350-A2 CHEMOKINE RECEPTOR BINDING COMPOUNDS ANORMED INC. (CA) 2006-12-28 WO 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-20210380539-A1 PARG INHIBITORY COMPOUNDS PARP11, PARG, PARP16 POLB 126/4885KMT2A 1566/4885CYP2C9 2487/4885
US-20230136702-A1 Inhibitors of Human Herpesviruses RPL5, RPL35, HAVCR2 POLB 1101/4885KMT2A 329/4885CYP2C9 4510/4885
US-12129236-B2 PARG inhibitory compounds PARP11, PARG, PARP16 POLB 126/4885KMT2A 1566/4885CYP2C9 2487/4885
US-20250223266-A1 PARG INHIBITORY COMPOUNDS PARG, PARP11, PARP16 POLB 141/4885KMT2A 1643/4885CYP2C9 2176/4885
US-20090099205-A1 Chemokine receptor binding compounds CCR5, CXCR3, CCL5 POLB 3133/4885KMT2A 4728/4885CYP2C9 4329/4885
US-20100286191-A1 2-Arylthiazole Derivatives as CXCR3 Receptor Modulators CXCR3, CXCR1, CXCR2 POLB 4548/4885KMT2A 3866/4885CYP2C9 1150/4885
US-20080132500-A1 Antibiotic compounds NRDC, MRPL21, PEPD POLB 2634/4885KMT2A 4616/4885CYP2C9 3260/4885

“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.