SCHEMBL14075951

SCHEMBL14075951

CC(C)(C)OC(=O)NCCN1CCN(C/C=C/C(=O)O)CC1

nearest known ligand 0.50

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ DRD2 P14416 11/20 0.50
▸ CACNA1H O95180 1/20 0.49
▸ SIGMAR1 Q99720 3/20 0.44
▸ MEN1 O00255 1/20 0.40
▸ GAA P10253 1/20 0.40
▸ KMT2A Q03164 1/20 0.40
▸ TDP1 Q9NUW8 1/20 0.39
▸ CD274 Q9NZQ7 1/20 0.39
▸ ALDH1A1 P00352 1/20 0.38
▸ GFER P55789 1/20 0.38

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
SCHEMBL14165710 1.00 DRD2 (0.50) DRD2CACNA1HSIGMAR1MEN1GAA
SCHEMBL16208607 0.90 DRD2 (0.50) DRD2CACNA1HSIGMAR1MEN1GAA
SCHEMBL21754610 0.88 DRD2 (0.52) DRD2CACNA1HSIGMAR1TDP1CD274
SCHEMBL22252842 0.88 DRD2 (0.49) DRD2CACNA1HSIGMAR1MEN1GAA
SCHEMBL20411791 0.85 DRD2 (0.47) DRD2CACNA1HSIGMAR1MEN1KMT2A
SCHEMBL31301242 0.84 DRD2 (0.63) DRD2CACNA1HSIGMAR1MEN1GAA
SCHEMBL20411793 0.84 DRD2 (0.50) DRD2CACNA1HSIGMAR1TDP1CD274
SCHEMBL25716981 0.83 DRD2 (0.54) DRD2CACNA1HSIGMAR1TDP1CD274
SCHEMBL13202614 0.80 DRD2 (0.59) DRD2CACNA1HSIGMAR1MEN1GAA
SCHEMBL31110037 0.79 DRD2 (0.55) DRD2CACNA1HSIGMAR1MEN1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250340560-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2025-11-06 — — US disclosed
US-12187687-B2 Compositions and uses thereof UNIVERSITY OF VIRGINIA PATENT FOUNDATION (US) 2025-01-07 — — US disclosed
US-20240270700-A1 COMPOSITIONS AND USES THEREOF UNIVERSITY OF VIRGINIA PATENT FOUNDATION 2024-08-15 — — US disclosed
US-20240254128-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2024-08-01 — — US disclosed
US-20230013862-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2023-01-19 — — US disclosed
US-20230013862-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BEIGENE SWITZERLAND GMBH (CH) 2023-01-19 — — US disclosed
EP-4056562-A1 HETEROCYCLIC INHIBITORS OF BRUTON'S TYROSINE KINASE Merck Patent GmbH (DE) 2022-09-14 — — EP disclosed
US-11142528-B2 Substituted pyrazolo[1,5-a]pyrimidines as Bruton's tyrosine kinase modulators BEIGENE SWITZERLAND GMBH (CH) 2021-10-12 — — US disclosed
US-11142528-B2 Substituted pyrazolo[1,5-a]pyrimidines as Bruton's tyrosine kinase modulators BEIGENE SWITZERLAND GMBH (CH) 2021-10-12 — — US disclosed
US-20200231551-A1 COMPOSITIONS AND USES THEREOF UNIVERSITY OF VIRGINIA 2020-07-23 — — US disclosed
WO-2015017502-A1 PYRIDINES, PYRIMIDINES, AND PYRAZINES, AS BTK INHIBITORS AND USES THEREOF MERCK PATENT GMBH (DE) 2015-02-05 — — WO disclosed
WO-2014173289-A1 FUSED HETEROCYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS BEIGENE, LTD. (KY) 2014-10-30 — — WO disclosed
US-20140162983-A1 Compositions and Methods for the Production of Pyrimidine and Pyridine Compounds with BTK Inhibitory Activity MERCK PATENT GMBH (DE) 2014-06-12 — — US disclosed
EP-2718270-A2 COMPOSITIONS AND METHODS FOR THE PRODUCTION OF PYRIMIDINE AND PYRIDINE COMPOUNDS WITH BTK INHIBITORY ACTIVITY Merck Patent GmbH (DE) 2014-04-16 — — EP disclosed
US-20130225812-A1 BRUTON'S TYROSINIE KINASE ACTIVITY PROBE AND METHOD OF USING PHARMACYCLICS, INC. (US) 2013-08-29 — — US disclosed
EP-2089391-B1 BRUTON'S TYROSINE KINASE ACTIVITY PROBE AND METHOD OF USING PHARMACYCLICS INC (US) 2013-01-16 — — EP disclosed
WO-2012170976-A2 COMPOSITIONS AND METHODS FOR THE PRODUCTION OF PYRIMIDINE AND PYRIDINE COMPOUNDS WITH BTK INHIBITORY ACTIVITY MERCK PATENT GMBH (DE) 2012-12-13 — — WO disclosed
US-20080214501-A1 Bruton's tyrosine kinase (Btk) activity probe comprising a Btk inhibitor moiety, a reporter moiety, and a linker moiety that links the inhibitor moiety to the reporter moiety; probes are used to characterize and develop Btk-selective inhibitors intended for therapeutic use PHARMACYCLICS, INC. (US) 2008-09-04 — — US disclosed
US-20080214501-A1 Bruton's tyrosine kinase (Btk) activity probe comprising a Btk inhibitor moiety, a reporter moiety, and a linker moiety that links the inhibitor moiety to the reporter moiety; probes are used to characterize and develop Btk-selective inhibitors intended for therapeutic use PHARMACYCLICS, INC. (US) 2008-09-04 — — US disclosed
WO-2008054827-A2 BRUTON'S TYROSINE KINASE ACTIVITY PROBE AND METHOD OF USING PHARMACYCLICS, INC. (US) 2008-05-08 — — 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 (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-20240270700-A1 COMPOSITIONS AND USES THEREOF CYP11B2, NQO1, CYP11B1 DRD2 4140/4885CACNA1H 4589/4885SIGMAR1 1168/4885
US-20130225812-A1 BRUTON'S TYROSINIE KINASE ACTIVITY PROBE AND METHOD OF USING BTK, SYK, LYN DRD2 4521/4885CACNA1H 3732/4885SIGMAR1 4400/4885
US-20240254128-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BTK, LCK, SYK DRD2 4861/4885CACNA1H 3300/4885SIGMAR1 3653/4885
US-20200231551-A1 COMPOSITIONS AND USES THEREOF CYP11B2, NQO1, CYP11B1 DRD2 4140/4885CACNA1H 4589/4885SIGMAR1 1168/4885
US-20080214501-A1 Bruton's tyrosine kinase (Btk) activity probe comprising a Btk inhibitor moiety, a reporter moiety, and a linker moiety that links the inhibitor moiety to the reporter moiety; probes are used to characterize and develop Btk-selective inhibitors intended for therapeutic use BTK, SYK, LYN DRD2 4210/4885CACNA1H 4474/4885SIGMAR1 4636/4885
US-12187687-B2 Compositions and uses thereof CYP11B2, CYP11B1, NQO1 DRD2 4180/4885CACNA1H 4521/4885SIGMAR1 899/4885
US-20140162983-A1 Compositions and Methods for the Production of Pyrimidine and Pyridine Compounds with BTK Inhibitory Activity BTK, SYK, LCK DRD2 4507/4885CACNA1H 4742/4885SIGMAR1 4714/4885
US-11142528-B2 Substituted pyrazolo[1,5-a]pyrimidines as Bruton's tyrosine kinase modulators BTK, LCK, SYK DRD2 4861/4885CACNA1H 3300/4885SIGMAR1 3653/4885
US-20230013862-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BTK, LCK, SYK DRD2 4861/4885CACNA1H 3300/4885SIGMAR1 3653/4885
US-20250340560-A1 SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINES AS BRUTON'S TYROSINE KINASE MODULATORS BTK, LCK, SYK DRD2 4861/4885CACNA1H 3300/4885SIGMAR1 3653/4885

“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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