SCHEMBL22150447

SCHEMBL22150447

O=C1CCC(N2C(=O)c3cccc(OCCOCCOCCOCc4ccccc4)c3C2=O)C(=O)N1

nearest known ligand 0.76

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
CRBN Q96SW2 16/20 0.76
DDB1 Q16531 14/20 0.76
IKZF3 Q9UKT9 6/20 0.58
MAP1LC3B Q9GZQ8 2/20 0.57
TNF P01375 1/20 0.56
IL1B P01584 1/20 0.56
TBXA2R P21731 1/20 0.56
IKZF1 Q13422 1/20 0.56
STAT3 P40763 1/20 0.55
ALDH1A1 P00352 1/20 0.53
CHRM2 P08172 1/20 0.53
OPRM1 P35372 1/20 0.53
CYP1A2 P05177 1/20 0.53
TSHR P16473 1/20 0.53
TDP1 Q9NUW8 1/20 0.53
AR P10275 1/20 0.52

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
SCHEMBL23133984 1.00 CRBN (0.76) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL23124803 1.00 CRBN (0.76) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL20294798 0.99 CRBN (0.75) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL20294800 0.99 CRBN (0.75) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL20294765 0.95 CRBN (0.75) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL20294768 0.95 CRBN (0.75) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL23302478 0.94 CRBN (0.76) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL24459261 0.90 CRBN (0.68) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL30862211 0.90 CRBN (0.68) CRBNDDB1IKZF3MAP1LC3BTNF
SCHEMBL29922394 0.90 CRBN (0.77) 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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250019371-A1 SMALL-MOLECULAR INHIBITORS FOR THE BETA-CATENIN/ B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. 2025-01-16 US disclosed
WO-2023077057-A1 SMALL-MOLECULAR INHIBITORS FOR THE BETA-CATENIN/ B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2023-05-04 WO disclosed
WO-2023077057-A1 SMALL-MOLECULAR INHIBITORS FOR THE BETA-CATENIN/ B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2023-05-04 WO disclosed
US-20220411372-A1 SMALL-MOLECULE INHIBITORS FOR THE B-CATENIN/B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. 2022-12-29 US disclosed
US-11236090-B2 Substituted glutarimides as CDK inhibitors SHANGHAI MEIZER PHARMACEUTICALS CO., LTD. (CN) 2022-02-01 US disclosed
US-20210363148-A1 COMPOUND HAVING BRUTON'S TYROSINE KINASE (BTK)-INHIBITION AND DEGRADATION ACTIVITY SHANGHAI MEIZER PHARMACEUTICALS CO LTD (CN) 2021-11-25 US disclosed
US-11155561-B2 Substituted glutarimides as Btk inhibitors SHANGHAI MEIZER PHARMACEUTICALS CO., LTD. (CN) 2021-10-26 US disclosed
WO-2021055936-A1 SMALL-MOLECULE INHIBITORS FOR THE Β-CATENIN/B-CELL LYMPHOMA 9 PROTEIN−PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2021-03-25 WO disclosed
WO-2021055936-A1 SMALL-MOLECULE INHIBITORS FOR THE Β-CATENIN/B-CELL LYMPHOMA 9 PROTEIN−PROTEIN INTERACTION H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2021-03-25 WO disclosed
US-20200216450-A1 COMPOUND FOR INHIBITING AND DEGRADING CDK SHANGHAI MEIZER PHARMACEUTICALS CO., LTD. (CN) 2020-07-09 US disclosed
EP-3677584-A1 COMPOUND HAVING BRUTON'S TYROSINE KINASE (BTK)-INHIBITION AND DEGRADATION ACTIVITY Shanghai Meizer Pharmaceuticals Co., Ltd. (CN) 2020-07-08 EP disclosed
US-20200199132-A1 COMPOUND HAVING BRUTON'S TYROSINE KINASE (BTK)-INHIBITION AND DEGRADATION ACTIVITY SHANGHAI MEIZER PHARMACEUTICALS CO., LTD. (CN) 2020-06-25 US disclosed
US-20200199106-A1 COMPOUND FOR INHIBITING AND DEGRADING TYROSINE PROTEIN KINASE ALK SHANGHAI MEIZER PHARMACEUTICALS CO., LTD. (CN) 2020-06-25 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 (8 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-20210363148-A1 COMPOUND HAVING BRUTON'S TYROSINE KINASE (BTK)-INHIBITION AND DEGRADATION ACTIVITY BTK, LYN, SYK CRBN 413/4885DDB1 1265/4885IKZF3 1314/4885
US-20220411372-A1 SMALL-MOLECULE INHIBITORS FOR THE B-CATENIN/B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION BCL9, BCL9L, BCL6 CRBN 444/4885DDB1 471/4885IKZF3 932/4885
US-20200199106-A1 COMPOUND FOR INHIBITING AND DEGRADING TYROSINE PROTEIN KINASE ALK ALK, BCR, BCL6 CRBN 183/4885DDB1 1835/4885IKZF3 966/4885
US-11155561-B2 Substituted glutarimides as Btk inhibitors BTK, SYK, GCDH CRBN 686/4885DDB1 940/4885IKZF3 1203/4885
US-20200216450-A1 COMPOUND FOR INHIBITING AND DEGRADING CDK CDK1, CDK6, CDK9 CRBN 790/4885DDB1 605/4885IKZF3 1512/4885
US-11236090-B2 Substituted glutarimides as CDK inhibitors CDKL1, CDKL2, CDK2 CRBN 1350/4885DDB1 219/4885IKZF3 3383/4885
US-20200199132-A1 COMPOUND HAVING BRUTON'S TYROSINE KINASE (BTK)-INHIBITION AND DEGRADATION ACTIVITY BTK, SYK, LYN CRBN 408/4885DDB1 1190/4885IKZF3 819/4885
US-20250019371-A1 SMALL-MOLECULAR INHIBITORS FOR THE BETA-CATENIN/ B-CELL LYMPHOMA 9 PROTEIN-PROTEIN INTERACTION BCL9, BCL9L, BCL6 CRBN 108/4885DDB1 138/4885IKZF3 506/4885

“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.