SCHEMBL2423601

SCHEMBL2423601

CC(C)(C)OC(=O)N1CC[C@@H](n2cc(B3OC(C)(C)C(C)(C)O3)cn2)C1

nearest known ligand 0.55

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
USP30 Q70CQ3 4/20 0.55
DDB1 Q16531 1/20 0.46
CRBN Q96SW2 1/20 0.46
FFAR1 O14842 1/20 0.41
SRC P12931 3/20 0.39
EGFR P00533 1/20 0.39
CCNC P24863 1/20 0.39
CDK8 P49336 1/20 0.39
GPR119 Q8TDV5 6/20 0.38
RECQL P46063 1/20 0.37

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
SCHEMBL2422527 1.00 USP30 (0.55) USP30DDB1CRBNFFAR1SRC
SCHEMBL2422530 1.00 USP30 (0.55) USP30DDB1CRBNFFAR1SRC
SCHEMBL1425502 0.94 USP30 (0.51) USP30DDB1CRBNFFAR1GPR119
SCHEMBL12539259 0.94 USP30 (0.51) USP30DDB1CRBNFFAR1GPR119
SCHEMBL1425500 0.94 USP30 (0.51) USP30DDB1CRBNFFAR1GPR119
SCHEMBL320828 0.94 USP30 (0.52) USP30DDB1CRBNFFAR1CCNC
SCHEMBL21602904 0.92 USP30 (0.48) USP30DDB1CRBNFFAR1SRC
SCHEMBL660078 0.92 USP30 (0.49) USP30DDB1CRBNFFAR1GPR119
SCHEMBL25238268 0.90 USP30 (0.49) USP30DDB1CRBNFFAR1EGFR
SCHEMBL15140394 0.88 USP30 (0.52) USP30DDB1CRBNFFAR1GPR119

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4719592-A1 BICYCLIC COMPOUNDS FOR KETOHEXOKINASE INHIBITION Centennial Therapeutics, LLC (US) 2026-04-08 EP disclosed
US-20250340533-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS TYRA BIOSCIENCES INC (US) 2025-11-06 US disclosed
US-12351571-B2 Substituted quinoxaline compounds as inhibitors of FGFR tyrosine kinases ARRAY BIOPHARMA INC. (US) 2025-07-08 US disclosed
US-12264149-B2 Indazole compounds as kinase inhibitors TYRA BIOSCIENCES, INC. (US) 2025-04-01 US disclosed
WO-2024253416-A1 PYRIMIDINE/PYRIDINE DERIVATIVES OR SALTS THEREOF AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE SAME YUHAN CORPORATION (KR) 2024-12-12 WO disclosed
WO-2024249612-A1 BICYCLIC COMPOUNDS FOR KETOHEXOKINASE INHIBITION CENTENNIAL THERAPEUTICS, LLC (US) 2024-12-05 WO disclosed
US-12071428-B2 Indazole compounds as kinase inhibitors TYRA BIOSCIENCES, INC. (US) 2024-08-27 US disclosed
US-20240208941-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS TYRA BIOSCIENCES, INC. 2024-06-27 US disclosed
US-11999722-B2 Disubstituted pyrazole compounds ELI LILLY AND COMPANY (US) 2024-06-04 US disclosed
US-20240109865-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS TYRA BIOSCIENCES, INC. 2024-04-04 US disclosed
US-20170362240-A1 4,6-SUBSTITUTED-PYRAZOLO[1,5-a]PYRAZINES AS JANUS KINASE INHIBITORS ARRAY BIOPHARMA INC. (US) 2017-12-21 US disclosed
EP-2265616-B1 FURO-AND THIENO[3,2-C]PYRIDINES OSI PHARM INC (US) 2013-11-20 EP disclosed
US-8178668-B2 2-aminopyridine kinase inhibitors OSI Pharmaceuticals, LLC (US) 2012-05-15 US disclosed
US-8022206-B2 Furo[3,2-C]pyridines OSI Pharmaceuticals, LLC (US) 2011-09-20 US disclosed
EP-2265270-A1 2-AMINOPYRIDINE KINASE INHIBITORS OSI Pharmaceuticals, Inc. (US) 2010-12-29 EP disclosed
EP-2265616-A1 FURO-AND THIENO[3,2-C]PYRIDINES OSI Pharmaceuticals, Inc. (US) 2010-12-29 EP disclosed
WO-2009100282-A1 FURO-AND THIENO[3,2-C] PYRIDINES OSI PHARMACEUTICALS, INC. (US) 2009-08-13 WO disclosed
WO-2009099982-A1 2-AMINOPYRIDINE KINASE INHIBITORS OSI PHARMACEUTICALS, INC. (US) 2009-08-13 WO disclosed
US-20090197864-A1 Furo- and Thieno [3,2-c] Pyridines OSI PHARMACEUTICALS, INC. 2009-08-06 US disclosed
US-20090197862-A1 2-AMINOPYRIDINE KINASE INHIBITORS OSI PHARMACEUTICALS, INC. 2009-08-06 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 (10 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-12071428-B2 Indazole compounds as kinase inhibitors FGFR1, FGFR2, FGFR3 USP30 3362/4885DDB1 1526/4885CRBN 1641/4885
US-20240208941-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS FGFR1, FGFR2, FGFR3 USP30 3362/4885DDB1 1526/4885CRBN 1641/4885
US-11999722-B2 Disubstituted pyrazole compounds SLC5A2, SLC5A1, GOT2 USP30 4494/4885DDB1 4540/4885CRBN 4623/4885
US-20170362240-A1 4,6-SUBSTITUTED-PYRAZOLO[1,5-a]PYRAZINES AS JANUS KINASE INHIBITORS JAK1, JAK3, JAK2 USP30 2445/4885DDB1 2741/4885CRBN 913/4885
US-20250340533-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS FGFR1, FGFR2, FGFR3 USP30 3362/4885DDB1 1526/4885CRBN 1641/4885
US-20090197864-A1 Furo- and Thieno [3,2-c] Pyridines RET, MET, ERBB2 USP30 3651/4885DDB1 2782/4885CRBN 414/4885
US-12264149-B2 Indazole compounds as kinase inhibitors FGFR1, FGFR2, FGFR3 USP30 3362/4885DDB1 1526/4885CRBN 1641/4885
US-12351571-B2 Substituted quinoxaline compounds as inhibitors of FGFR tyrosine kinases FGFR3, FGFR4, FGFR1 USP30 2688/4885DDB1 1067/4885CRBN 1536/4885
US-20090197862-A1 2-AMINOPYRIDINE KINASE INHIBITORS ERBB2, ABL2, TIE1 USP30 4472/4885DDB1 3218/4885CRBN 2509/4885
US-20240109865-A1 INDAZOLE COMPOUNDS AS KINASE INHIBITORS FGFR1, FGFR2, FGFR3 USP30 3362/4885DDB1 1526/4885CRBN 1641/4885

“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.