SCHEMBL778980

SCHEMBL778980

CC(C)(C)OC(=O)N1CCN(C(=O)OCc2ccccc2)C(CO)C1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP1 P09874 1/20 0.58
PDK1 Q15118 1/20 0.53
PDK2 Q15119 1/20 0.53
PDK3 Q15120 1/20 0.53
PDK4 Q16654 1/20 0.53
JAK2 O60674 1/20 0.46
JAK1 P23458 1/20 0.46
ABHD6 Q9BV23 1/20 0.46
DAGLA Q9Y4D2 1/20 0.46
OPRK1 P41145 1/20 0.45
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45
NPC1 O15118 2/20 0.44
RAB9A P51151 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
HTT P42858 1/20 0.44
NR1H2 P55055 2/20 0.44
NR1H3 Q13133 2/20 0.44
GPR119 Q8TDV5 1/20 0.44
STS P08842 1/20 0.43

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
SCHEMBL4828910 1.00 PARP1 (0.58) PARP1PDK1PDK2PDK3PDK4
SCHEMBL17068124 1.00 PARP1 (0.58) PARP1PDK1PDK2PDK3PDK4
SCHEMBL6334954 0.96 PARP1 (0.63) PARP1PDK1PDK2PDK3PDK4
SCHEMBL2420439 0.96 PARP1 (0.63) PARP1PDK1PDK2PDK3PDK4
SCHEMBL20129602 0.96 PARP1 (0.63) PARP1PDK1PDK2PDK3PDK4
SCHEMBL22034240 0.94 PARP1 (0.54) PARP1PDK1PDK2PDK3PDK4
SCHEMBL7496827 0.91 PARP1 (0.56) PARP1PDK1PDK2PDK3PDK4
SCHEMBL7494554 0.91 PARP1 (0.56) PARP1PDK1PDK2PDK3PDK4
SCHEMBL19959259 0.91 PARP1 (0.58) PARP1PDK1PDK2PDK3PDK4
SCHEMBL21594462 0.91 PARP1 (0.63) PARP1PDK1PDK2PDK3PDK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250304568-A1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE ABBVIE INC (US) 2025-10-02 US disclosed
US-12319679-B2 Morpholinyl, piperazinyl, oxazepanyl and diazepanyl O-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors BIOGEN MA INC. (US) 2025-06-03 US disclosed
EP-4480482-A2 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE AbbVie Inc. (US) 2024-12-25 EP disclosed
US-12172992-B2 Pyrimidines for degrading Bruton's tyrosine kinase ABBVIE INC. (US) 2024-12-24 US disclosed
EP-4249073-B1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE ABBVIE INC (US) 2024-12-11 EP disclosed
US-20240109877-A1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE ABBVIE INC. 2024-04-04 US disclosed
EP-4327814-A2 MORPHOLINYL, PIPERAZINYL, OXAZEPANYL AND DIAZEPANYL O-GLYCOPROTEIN-2-ACETAMIDO-2-DEOXY-3-D-GLUCOPYRANOSIDASE INHIBITORS Biogen MA Inc. (US) 2024-02-28 EP disclosed
EP-4294800-A1 APOL1 INHIBITORS AND METHODS OF USE Maze Therapeutics, Inc. (US) 2023-12-27 EP disclosed
CN-117083274-A Fused ring heterocyclic derivative and application thereof in medicine 四川海思科制药有限公司 2023-11-17 CN disclosed
WO-2023183811-A1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE ABBVIE INC. (US) 2023-09-28 WO disclosed
EP-1206265-B1 SRC KINASE INHIBITOR COMPOUNDS MERCK & CO INC (US) 2003-11-12 EP disclosed
WO-2003041711-A1 PIPERAZINE BIS-AMIDE DERIVATIVES AND THEIR USE AS ANTAGONISTS OF THE OREXIN RECEPTOR SMITHKLINE BEECHAM P.L.C. (GB) 2003-05-22 WO disclosed
US-6498165-B1 PYRIMIDINE COMPOUNDS; PROPHYLAXIS AND TREATMENT OF SUCH AS IMMUNE DISEASES, HYPERPROLIFERATIVE DISORDERS, CANCER, ANGIOGENSIS, ATHEROSCELEROSIS, GRAFT REJECTION, RHEUMATOID ARTHRITIS, PSORIASIS MERCK & CO., INC. 2002-12-24 US disclosed
EP-1194152-A4 SRC KINASE INHIBITOR COMPOUNDS MERCK & CO INC (US) 2002-11-06 EP disclosed
EP-1206265-A4 SRC KINASE INHIBITOR COMPOUNDS MERCK & CO INC (US) 2002-08-07 EP disclosed
EP-1206265-A1 SRC KINASE INHIBITOR COMPOUNDS Merck & Co., Inc. (US) 2002-05-22 EP disclosed
EP-1194152-A1 SRC KINASE INHIBITOR COMPOUNDS Merck & Co., Inc. (US) 2002-04-10 EP disclosed
US-6316444-B1 SRC kinase inhibitor compounds MERCK & CO., INC. 2001-11-13 US disclosed
WO-2001000213-A1 SRC KINASE INHIBITOR COMPOUNDS MERCK & CO., INC. (US) 2001-01-04 WO disclosed
WO-2001000214-A1 SRC KINASE INHIBITOR COMPOUNDS MERCK & CO., INC. (US) 2001-01-04 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 (4 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-20250304568-A1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE BTK, TYMP, LYN PARP1 404/4885PDK1 1176/4885PDK2 725/4885
US-20240109877-A1 PYRIMIDINES FOR DEGRADING BRUTON'S TYROSINE KINASE BTK, TYMP, LYN PARP1 404/4885PDK1 1176/4885PDK2 725/4885
US-12319679-B2 Morpholinyl, piperazinyl, oxazepanyl and diazepanyl O-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors MAN2A1, MAN2B2, MGAT3 PARP1 3527/4885PDK1 1670/4885PDK2 1099/4885
US-12172992-B2 Pyrimidines for degrading Bruton's tyrosine kinase BTK, TYMP, LYN PARP1 404/4885PDK1 1176/4885PDK2 725/4885

“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.