SCHEMBL845548

SCHEMBL845548

CN1C(=O)CCC(N2C(=O)c3ccccc3C2=O)C1=O

nearest known ligand 0.54

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
CRBN Q96SW2 15/20 0.54
DDB1 Q16531 11/20 0.54
IKZF3 Q9UKT9 2/20 0.54
TSHR P16473 2/20 0.54
ALDH1A1 P00352 1/20 0.54
CHRM2 P08172 1/20 0.54
OPRM1 P35372 1/20 0.54
CYP1A2 P05177 1/20 0.54
TDP1 Q9NUW8 1/20 0.54
TNF P01375 1/20 0.42
IL1B P01584 1/20 0.42
TBXA2R P21731 1/20 0.42
IKZF1 Q13422 1/20 0.42
CASP3 P42574 1/20 0.41
KMT2A Q03164 1/20 0.39

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
SCHEMBL17197939 0.86 CRBN (0.45) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL22940384 0.84 CRBN (0.62) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL9988681 0.84 DDB1 (0.60) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL12809078 0.84 CRBN (0.51) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL21341598 0.84 CRBN (0.43) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL21062845 0.83 CRBN (0.60) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL21196697 0.83 DDB1 (0.60) CRBNDDB1IKZF3TNFIL1B
SCHEMBL32679446 0.83 CRBN (0.60) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL29589619 0.83 CRBN (0.59) CRBNDDB1IKZF3TSHRALDH1A1
SCHEMBL21331544 0.83 CRBN (0.59) CRBNDDB1TSHRALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118027003-A PROTAC compound, preparation method thereof and application of PROTAC compound as estrogen receptor degradation agent 山东大学 2024-05-14 CN claimed
CN-117836299-A Novel bifunctional heterocyclic compounds with Bruton tyrosine kinase decomposition via ubiquitin proteasome pathway and uses thereof 韩国化学研究院 2024-04-05 CN claimed
WO-1992014455-A1 METHOD FOR CONTROLLING ABNORMAL CONCENTRATION TNF α IN HUMAN TISSUES THE ROCKEFELLER UNIVERSITY (US) 1992-09-03 WO claimed
CN-122029163-A Chemical for targeting chromatin remodeling complexes and uses thereof 丹娜-法伯癌症研究院 2026-05-12 CN disclosed
US-12564583-B2 Small molecules against cereblon to enhance effector T cell function Lee Moffitt Cancer Center and Research Institute, Inc. (US) 2026-03-03 US disclosed
US-20250368640-A1 MULTIPLE KINASE DEGRADERS, COMPOSITIONS COMPRISING THE DEGRADER, AND METHODS OF USING THE SAME BIOFRONT LTD (KY) 2025-12-04 US disclosed
EP-4629981-A2 SMALL MOLECULE DEGRADERS OF C-SRC KINASE The Regents Of The University Of Michigan (US) 2025-10-15 EP disclosed
US-20250127903-A1 SUBSTITUTED PIPERIDINE DEGRONIMERS FOR TARGET PROTEIN DEGRADATION C4 THERAPEUTICS, INC. (US) 2025-04-24 US disclosed
EP-4540246-A1 MULTIPLE KINASE DEGRADERS, COMPOSITIONS COMPRISING THE DEGRADER, AND METHODS OF USING THE SAME BIOFRONT LTD (KY) 2025-04-23 EP disclosed
CN-119751533-A Estrogen receptor protein targeted degradation chimeric derivative based on estratriene structure, and preparation method and application thereof 山东大学 2025-04-04 CN disclosed
US-20250051347-A1 BIFUNCTIONAL CHIMERIC HETEROCYCLIC COMPOUND AND USE THEREOF AS ANDROGEN RECEPTOR DEGRADER Hinova Pharmaceuticals, Inc. (CN) 2025-02-13 US disclosed
EP-1903873-A2 HERPES VIRUS-BASED COMPOSITIONS AND METHODS OF USE IN THE PRENATAL AND PERINATAL PERIODS THE UNIVERSITY OF ROCHESTER (US) 2008-04-02 EP disclosed
US-20080070303-A1 Using myocardial and/or muscle progenitor cells as modeling tool in tissue engineering; regenerative medicine and organ replacement ADVANCED CELL TECHNOLOGY 2008-03-20 US disclosed
EP-1853302-A2 ANTIANGIOGENIC AGENTS WITH ALDESLEUKIN Novartis Vaccines and Diagnostics, Inc. (US) 2007-11-14 EP disclosed
US-20070197791-A1 Method for the preparation of dicarboxylic lmides SIEGFRIED LTD. (CH) 2007-08-23 US disclosed
WO-2007062198-A1 METHODS TO ACCELERATE THE ISOLATION OF NOVEL CELL STRAINS FROM PLURIPOTENT STEM CELLS AND CELLS OBTAINED THEREBY ADVANCED CELL TECHNOLOGY, INC. (US) 2007-05-31 WO disclosed
US-20070021464-A1 Methods and compositions for inhibition of angiogenesis with EM-12 Derivatives D AMATO ROBERT 2007-01-25 US disclosed
WO-2006135602-A2 HERPES VIRUS-BASED COMPOSITIONS AND METHODS OF USE IN THE PRENATAL AND PERINATAL PERIODS UNIVERSITY OF ROCHESTER (US) 2006-12-21 WO disclosed
WO-2006089150-A2 ANTIANGIOGENIC AGENTS WITH ALDESLEUKIN NOVARTIS VACCINES AND DIAGNOSTICS INC. (US) 2006-08-24 WO disclosed
WO-1992014455-A1 METHOD FOR CONTROLLING ABNORMAL CONCENTRATION TNF α IN HUMAN TISSUES THE ROCKEFELLER UNIVERSITY (US) 1992-09-03 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 (6 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-12564583-B2 Small molecules against cereblon to enhance effector T cell function CRBN, CD4, ICOS CRBN 1/4885DDB1 2979/4885IKZF3 80/4885
US-20250127903-A1 SUBSTITUTED PIPERIDINE DEGRONIMERS FOR TARGET PROTEIN DEGRADATION STUB1, UBE3C, NEDD4 CRBN 77/4885DDB1 769/4885IKZF3 2159/4885
US-20250368640-A1 MULTIPLE KINASE DEGRADERS, COMPOSITIONS COMPRISING THE DEGRADER, AND METHODS OF USING THE SAME MAP4K1, MAP4K4, MAP4K5 CRBN 1379/4885DDB1 1741/4885IKZF3 1428/4885
US-20250051347-A1 BIFUNCTIONAL CHIMERIC HETEROCYCLIC COMPOUND AND USE THEREOF AS ANDROGEN RECEPTOR DEGRADER AR, ADRM1, MDM2 CRBN 619/4885DDB1 2893/4885IKZF3 755/4885
US-20070197791-A1 Method for the preparation of dicarboxylic lmides RPL3, CCNH, CCNB3 CRBN 17/4885DDB1 2008/4885IKZF3 1533/4885
US-20070021464-A1 Methods and compositions for inhibition of angiogenesis with EM-12 Derivatives EDF1, FLT4, EML4 CRBN 272/4885DDB1 412/4885IKZF3 2960/4885

“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.