SCHEMBL1673620

SCHEMBL1673620

CC(C)(C)OC(=O)N1CCCC(c2ccc(Br)cc2)C1

nearest known ligand 0.55

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
FPR2 P25090 6/20 0.55
PDE4B Q07343 1/20 0.52
RORC P51449 2/20 0.51
FPR3 P25089 3/20 0.50
HPGDS O60760 1/20 0.47
CHRNA7 P36544 1/20 0.46
MEN1 O00255 1/20 0.46
ALDH1A1 P00352 1/20 0.46
MAPT P10636 1/20 0.46
KMT2A Q03164 1/20 0.46
JAK2 O60674 1/20 0.46
JAK1 P23458 1/20 0.46
NAMPT P43490 1/20 0.46
TRPV3 Q8NET8 1/20 0.46
USP30 Q70CQ3 2/20 0.45
HSD11B1 P28845 1/20 0.45

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
SCHEMBL28943526 1.00 FPR2 (0.55) FPR2PDE4BRORCFPR3HPGDS
SCHEMBL18557979 1.00 FPR2 (0.55) FPR2PDE4BRORCFPR3HPGDS
SCHEMBL1015281 0.93 PDE4B (0.58) FPR2PDE4BRORCFPR3ALDH1A1
SCHEMBL1015283 0.93 PDE4B (0.58) FPR2PDE4BRORCFPR3ALDH1A1
SCHEMBL18509294 0.88 GPR119 (0.54) PDE4BHPGDSMEN1ALDH1A1MAPT
SCHEMBL20748135 0.88 PDE4B (0.53) FPR2PDE4BHPGDSMEN1ALDH1A1
SCHEMBL15187965 0.88 RORC (0.56) FPR2PDE4BRORCFPR3NAMPT
SCHEMBL1422394 0.87 PDE4B (0.52) PDE4BHPGDSMEN1ALDH1A1MAPT
SCHEMBL1988650 0.87 PDE4B (0.52) PDE4BHPGDSMEN1ALDH1A1MAPT
SCHEMBL22810473 0.87 PDE4B (0.52) PDE4BRORCHPGDSMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115626891-B Synthesis method of nilaparib key intermediate 四川轻化工大学 2024-01-26 CN claimed
CN-115626891-A Synthesis method of nilapanib key intermediate 四川轻化工大学 2023-01-20 CN claimed
EP-4712969-A1 CYCLIN INHIBITORS Circle Pharma, Inc. (US) 2026-03-25 EP disclosed
EP-4709730-A1 HETEROARYL COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK4 Celgene Corporation (US) 2026-03-18 EP disclosed
CN-119751337-A Preparation method of high-purity nilaparib intermediate 南京唯创远医药科技有限公司 2025-04-04 CN disclosed
US-20240408169-A1 CYCLIN INHIBITORS CIRCLE PHARMA, INC. 2024-12-12 US disclosed
WO-2024233742-A1 HETEROARYL COMPOUNDS AS LIGAND DIRECTED DEGRADERS OF IRAK4 CELGENE CORPORATION (US) 2024-11-14 WO disclosed
CN-115626891-B Synthesis method of nilaparib key intermediate 四川轻化工大学 2024-01-26 CN disclosed
CN-115626891-B Synthesis method of nilaparib key intermediate 四川轻化工大学 2024-01-26 CN disclosed
CN-114957101-B Synthesis method of 3-aryl substituted dipiperidone and nilaparil 山东第一医科大学(山东省医学科学院) 2023-11-28 CN disclosed
CN-113461597-B Preparation method of nilaparib intermediate 天津太平洋化学制药有限公司 2023-07-21 CN disclosed
US-20120245172-A1 HETEROCYCLIC AMINE DERIVATIVES HOFFMANN-LA ROCHE INC. 2012-09-27 US disclosed
US-20120245172-A1 HETEROCYCLIC AMINE DERIVATIVES HOFFMANN-LA ROCHE INC. 2012-09-27 US disclosed
WO-2011123419-A1 TRYCYCLIC COMPOUNDS AND PBK INHIBITORS CONTAINING THE SAME ONCOTHERAPY SCIENCE, INC. (JP) 2011-10-06 WO disclosed
EP-2308854-A1 2,3,6-trisubstituted-4-pyrimidone derivatives Sanofi-Aventis (FR) 2011-04-13 EP disclosed
EP-2305651-A1 2,3,6-trisubstituted-4-pyrimidone derivatives Mitsubishi Tanabe Pharma Corporation (JP) 2011-04-06 EP disclosed
US-7504411-B2 2,3,6-Trisubstituted-4-pyrimidone derivatives MITSUBISHI TANABE PHARMA CORPORATION (JP) 2009-03-17 US disclosed
US-20060252768-A1 2,3,6-Trisubstituted-4-pyrimidone derivatives SANOFI (FR) 2006-11-09 US disclosed
EP-1608630-A1 2, 3, 6-TRISUBSTITUTED-4-PYRIMIDONE DERIVATIVES Mitsubishi Pharma Corporation (JP) 2005-12-28 EP disclosed
WO-2004085408-A1 2, 3, 6-TRISUBSTITUTED-4-PYRIMIDONE DERIVATIVES MITSUBISHI PHARMA CORPORATION (JP) 2004-10-07 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 (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-20120245172-A1 HETEROCYCLIC AMINE DERIVATIVES TAAR1, TAAR5, MTNR1A FPR2 2048/4885PDE4B 672/4885RORC 524/4885
US-20240408169-A1 CYCLIN INHIBITORS CCNI, CDK2, CDK1 FPR2 4502/4885PDE4B 3643/4885RORC 646/4885
US-20060252768-A1 2,3,6-Trisubstituted-4-pyrimidone derivatives PSEN1, PSEN2, MAPT FPR2 3254/4885PDE4B 3748/4885RORC 1594/4885

“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.