SCHEMBL29360230

SCHEMBL29360230

O=C(O)COc1cccc2c1C(=O)N(C1CCC(=O)NC1=O)C2=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CRBN Q96SW2 17/20 1.00
▸ DDB1 Q16531 16/20 1.00
▸ IKZF3 Q9UKT9 3/20 0.61
▸ TNF P01375 1/20 0.61
▸ IL1B P01584 1/20 0.61
▸ TBXA2R P21731 1/20 0.61
▸ IKZF1 Q13422 1/20 0.61
▸ ALDH1A1 P00352 1/20 0.58
▸ CHRM2 P08172 1/20 0.58
▸ OPRM1 P35372 1/20 0.58
▸ CYP1A2 P05177 1/20 0.58
▸ TSHR P16473 1/20 0.58
▸ TDP1 Q9NUW8 1/20 0.58
▸ STAT3 P40763 2/20 0.58
▸ HDAC3 O15379 1/20 0.56
▸ HDAC4 P56524 1/20 0.56
▸ HDAC1 Q13547 1/20 0.56
▸ HDAC2 Q92769 1/20 0.56
▸ HDAC6 Q9UBN7 1/20 0.56
▸ NCOR2 Q9Y618 1/20 0.56

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
SCHEMBL14085581 1.00 CRBN (1.00) CRBNDDB1IKZF3TNFIL1B
SCHEMBL24377001 0.91 CRBN (0.84) CRBNDDB1IKZF3TNFIL1B
SCHEMBL29622415 0.91 CRBN (0.84) CRBNDDB1IKZF3TNFIL1B
SCHEMBL30850501 0.91 CRBN (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL24621043 0.91 CRBN (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL18379320 0.91 CRBN (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL17884453 0.91 CRBN (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL18379436 0.91 CRBN (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL19481530 0.91 DDB1 (0.83) CRBNDDB1IKZF3TNFIL1B
SCHEMBL30850474 0.90 CRBN (0.82) CRBNDDB1IKZF3TNFIL1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024145315-A1 TARGETED PROTEIN DEGRADERS OF INDOLEAMINE 2,3-DIOXYGENASE 1 (IDO1) NORTHWESTERN UNIVERSITY (US) 2024-07-04 — — WO claimed
WO-2023215321-A2 POLYNUCLEOTIDE COMPOSITIONS FOR THE TREATMENT OF PREMATURE TERMINATION DISEASES CONFLUENCE THERAPEUTICS, INC. (US) 2023-11-09 — — WO claimed
US-20230312639-A1 GPER PROTEOLYTIC TARGETING CHIMERAS UNIVERSITY OF IOWA RESEARCH FOUNDATION 2023-10-05 — — US claimed
EP-4138921-A1 GPER PROTEOLYTIC TARGETING CHIMERAS University Of Iowa Research Foundation (US) 2023-03-01 — — EP claimed
US-20220023431-A1 PROTEOLYSIS-TARGETING CHIMERIC MOLECULES (PROTACS) THAT INDUCE DEGRADATION OF INDOLEAMINE 2,3-DIOXYGENASE (IDO) PROTEIN NORTHWESTERN UNIVERSITY 2022-01-27 — — US claimed
US-20260131010-A1 MENIN PROTEOLYSIS TARGETING CHIMERAS (PROTACS) UNIV TEXAS (US) 2026-05-14 — — US disclosed
US-20260053934-A1 DUAL ACTION ONLY PROTEOLYSIS TARGETING CHIMERAS AND USES THEREOF UNIV MASSACHUSETTS (US) 2026-02-26 — — US disclosed
US-12492209-B2 Substituted [1,2,4]triazolo[4,3-c]pyrimidines that induce degradation of embryonic ectoderm development (EED) protein NORTHWESTERN UNIVERSITY (US) 2025-12-09 — — US disclosed
US-12491252-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 NORTHWESTERN UNIVERSITY (US) 2025-12-09 — — US disclosed
EP-4615869-A1 COMBINATION THERAPY COMPRISING BISPECIFIC ANTIBODIES COMPRISING AN NRP1 BINDING DOMAIN Pinetree Therapeutics, Inc. (US) 2025-09-17 — — EP disclosed
US-12311029-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein NORTHWESTERN UNIVERSITY (US) 2025-05-27 — — US disclosed
CN-119732914-A Nanometer degradation agent based on proteolytic targeting chimeric molecule, preparation method and application thereof 中国科学院长春应用化学研究所 2025-04-01 — — CN disclosed
US-11890346-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of c-MYC protein NORTHWESTERN UNIVERSITY (US) 2024-02-06 — — US disclosed
WO-2023215321-A2 POLYNUCLEOTIDE COMPOSITIONS FOR THE TREATMENT OF PREMATURE TERMINATION DISEASES CONFLUENCE THERAPEUTICS, INC. (US) 2023-11-09 — — WO disclosed
US-20230346953-A1 SUBSTITUTED 3-AMINO-5-PHENYLBENZAMIDE COMPOUNDS AS COVALENT INHIBITORS OF ENHANCER ZESTE HOMOLOG 2 (EZH2) AND PROTEOLYSIS-TARGETING CHIMERIC DERIVATIVES THEREOF (PROTACS) THAT INDUCE DEGRADATION OF EZH2 UNITED STATES GOVERNMENT 2023-11-02 — — US disclosed
US-20230312639-A1 GPER PROTEOLYTIC TARGETING CHIMERAS UNIVERSITY OF IOWA RESEARCH FOUNDATION 2023-10-05 — — US disclosed
WO-2023074780-A1 THERAPEUTIC AGENT COMPOSITION 国立大学法人愛媛大学 2023-05-04 — — WO disclosed
EP-4138921-A1 GPER PROTEOLYTIC TARGETING CHIMERAS University Of Iowa Research Foundation (US) 2023-03-01 — — EP disclosed
WO-2022185319-A1 UBIQUITIN LIGASE KPC1-PEPTIDE BASED PROTEOLYSIS TARGETING CHIMERAS (PROTAC) AND USES THEREOF TECHNION RESEARCH & DEVELOPMENT FOUNDATION LIMITED (IL) 2022-09-09 — — WO disclosed
US-20220023431-A1 PROTEOLYSIS-TARGETING CHIMERIC MOLECULES (PROTACS) THAT INDUCE DEGRADATION OF INDOLEAMINE 2,3-DIOXYGENASE (IDO) PROTEIN NORTHWESTERN UNIVERSITY 2022-01-27 — — 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 (9 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-12311029-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein IDO1, IDO2, KMO CRBN 95/4885DDB1 1376/4885IKZF3 151/4885
US-20230312639-A1 GPER PROTEOLYTIC TARGETING CHIMERAS GPER1, ESR1, ADRM1 CRBN 658/4885DDB1 1582/4885IKZF3 1524/4885
US-20260131010-A1 MENIN PROTEOLYSIS TARGETING CHIMERAS (PROTACS) CRBN, UBE3C, PSME3 CRBN 1/4885DDB1 757/4885IKZF3 744/4885
US-12492209-B2 Substituted [1,2,4]triazolo[4,3-c]pyrimidines that induce degradation of embryonic ectoderm development (EED) protein EED, CUL3, PSME3 CRBN 73/4885DDB1 923/4885IKZF3 433/4885
US-20230346953-A1 SUBSTITUTED 3-AMINO-5-PHENYLBENZAMIDE COMPOUNDS AS COVALENT INHIBITORS OF ENHANCER ZESTE HOMOLOG 2 (EZH2) AND PROTEOLYSIS-TARGETING CHIMERIC DERIVATIVES THEREOF (PROTACS) THAT INDUCE DEGRADATION OF EZH2 EZH2, BAZ2A, BAZ2B CRBN 33/4885DDB1 613/4885IKZF3 91/4885
US-20260053934-A1 DUAL ACTION ONLY PROTEOLYSIS TARGETING CHIMERAS AND USES THEREOF PSMA1, PSMB1, PSME1 CRBN 77/4885DDB1 1611/4885IKZF3 503/4885
US-20220023431-A1 PROTEOLYSIS-TARGETING CHIMERIC MOLECULES (PROTACS) THAT INDUCE DEGRADATION OF INDOLEAMINE 2,3-DIOXYGENASE (IDO) PROTEIN IDO1, IDO2, KMO CRBN 176/4885DDB1 1197/4885IKZF3 151/4885
US-12491252-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 EZH2, BAZ2A, BAZ2B CRBN 33/4885DDB1 613/4885IKZF3 91/4885
US-11890346-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of c-MYC protein MYCBP, MYC, MYCBP2 CRBN 6/4885DDB1 743/4885IKZF3 298/4885

“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.

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