SCHEMBL3718600

SCHEMBL3718600

O=Cc1ccc(OCC2CC2)cc1

nearest known ligand 0.54

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
PARP15 Q460N3 5/20 0.54
PARP10 Q53GL7 5/20 0.54
PARP2 Q9UGN5 2/20 0.54
HPGD P15428 6/20 0.50
ALDH1A1 P00352 4/20 0.46
LMNA P02545 1/20 0.46
MAPT P10636 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
CYP2A6 P11509 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
KDM4E B2RXH2 1/20 0.44
SIGMAR1 Q99720 1/20 0.44

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
SCHEMBL8312964 1.00 PARP15 (0.54) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL8314306 1.00 PARP15 (0.54) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL22820830 0.95 PARP15 (0.50) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL6686905 0.94 PARP15 (0.58) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL1299143 0.93 HPGD (0.58) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL1299517 0.92 HPGD (0.61) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL1299658 0.91 HPGD (0.59) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL10906512 0.91 HPGD (0.59) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL3067625 0.90 PARP15 (0.54) PARP15PARP10PARP2HPGDALDH1A1
SCHEMBL28371333 0.88 ALDH1A1 (0.50) PARP15PARP10PARP2HPGDALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260035361-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) SHANGHAI DEGRON BIOMEDICAL TECH CO LTD (CN) 2026-02-05 US disclosed
US-12528773-B2 Non-lysosomal glucosylceramidase inhibitors and uses thereof ALECTOS THERAPEUTICS INC. (CA) 2026-01-20 US disclosed
EP-4626880-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) Shanghai Degron Biomedical Technology Co., Ltd. (CN) 2025-10-08 EP disclosed
EP-4622647-A1 RNA DEGRADERS AND USES THEREOF Arrakis Therapeutics, Inc. (US) 2025-10-01 EP disclosed
EP-4021901-B1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL MYERS SQUIBB CO (US) 2025-09-24 EP disclosed
US-20240400563-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS BRISTOL-MYERS SQUIBB COMPANY 2024-12-05 US disclosed
WO-2024114639-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) SHANGHAI DEGRON BIOMEDICAL TECHNOLOGY CO., LTD. (CN) 2024-06-06 WO disclosed
CN-114302884-B Substituted pyridopyrimidinone compounds useful as T cell activators 百时美施贵宝公司 2024-06-04 CN disclosed
WO-2024112918-A1 RNA DEGRADERS AND USES THEREOF ARRAKIS THERAPEUTICS, INC. (US) 2024-05-30 WO disclosed
CN-112654621-B Substituted naphthyridinone compounds useful as T cell activators 百时美施贵宝公司 2024-05-14 CN disclosed
EP-2881384-A1 PARTIALLY SATURATED NITROGEN-CONTAINING HETEROCYCLIC COMPOUND Taisho Pharmaceutical Co., Ltd. (JP) 2015-06-10 EP disclosed
CN-104507910-A Partially saturated nitrogen-containing heterocyclic compound TAISHO PHARMACEUTICAL CO LTD 2015-04-08 CN disclosed
CN-102015715-A Fused pyrimidones as TRPV3 modulators GLENMARK PHARMACEUTICALS SA 2011-04-13 CN disclosed
WO-2010127212-A1 INHIBITORS OF ACETYL-COA CARBOXYLASE FOREST LABORATORIES HOLDINGS LIMITED (BM) 2010-11-04 WO disclosed
US-20100280067-A1 INHIBITORS OF ACETYL-COA CARBOXYLASE SARMA PAKALA KUMARA SAVITHRU 2010-11-04 US disclosed
US-20090221649-A1 Use of substituted 2-thio-3,5-dicyano-4-phenyl-6-aminopyridines for the treatment of reperfusion injury and reperfusion damage BAYER HEALTHCARE AG (DE) 2009-09-03 US disclosed
US-20090221649-A1 Use of substituted 2-thio-3,5-dicyano-4-phenyl-6-aminopyridines for the treatment of reperfusion injury and reperfusion damage BAYER HEALTHCARE AG (DE) 2009-09-03 US disclosed
US-20090221649-A1 Use of substituted 2-thio-3,5-dicyano-4-phenyl-6-aminopyridines for the treatment of reperfusion injury and reperfusion damage BAYER HEALTHCARE AG (DE) 2009-09-03 US disclosed
EP-1863482-A1 USE OF SUBSTITUTED 2-THIO-3,5-DICYANO-4-PHENYL-6-AMINOPYRIDINES FOR THE TREATMENT OF REPERFUSION INJURY AND REPERFUSION DAMAGE Bayer HealthCare AG (DE) 2007-12-12 EP disclosed
WO-2006099958-A1 USE OF SUBSTITUTED 2-THIO-3,5-DICYANO-4-PHENYL-6-AMINOPYRIDINES FOR THE TREATMENT OF REPERFUSION INJURY AND REPERFUSION DAMAGE BAYER HEALTHCARE AG (DE) 2006-09-28 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 (5 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-12528773-B2 Non-lysosomal glucosylceramidase inhibitors and uses thereof GBA1, GBA2, GAA PARP15 4010/4885PARP10 3942/4885PARP2 4231/4885
US-20240400563-A1 SUBSTITUTED PYRIDOPYRIMIDINONYL COMPOUNDS USEFUL AS T CELL ACTIVATORS DGKZ, DGKA, DGKG PARP15 1689/4885PARP10 1518/4885PARP2 2439/4885
US-20090221649-A1 Use of substituted 2-thio-3,5-dicyano-4-phenyl-6-aminopyridines for the treatment of reperfusion injury and reperfusion damage TNNI3, CASP3, GOT2 PARP15 1341/4885PARP10 2576/4885PARP2 905/4885
US-20100280067-A1 INHIBITORS OF ACETYL-COA CARBOXYLASE ACACA, ACACB, PC PARP15 419/4885PARP10 607/4885PARP2 643/4885
US-20260035361-A1 COMPOUNDS FOR MODULATING HUR (ELAVL1) ELAVL1, ELAVL3, HNRNPL PARP15 3662/4885PARP10 3592/4885PARP2 3405/4885

“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.