SCHEMBL4295685

SCHEMBL4295685

COC(=O)C1(CO)CCN(C(=O)OC(C)(C)C)CC1

nearest known ligand 0.53

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
PKM P14618 1/20 0.49
USP2 O75604 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
CYP4F2 P78329 1/20 0.44
CYP4A11 Q02928 1/20 0.44
MMP13 P45452 3/20 0.42
ADAM17 P78536 3/20 0.42
MMP2 P08253 2/20 0.42
EPHX2 P34913 1/20 0.42
EPHX1 P07099 1/20 0.40
NR1H2 P55055 1/20 0.40
MMP14 P50281 1/20 0.40
HPGD P15428 1/20 0.39
GPR119 Q8TDV5 1/20 0.39

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
SCHEMBL12193909 0.91 CYP4F2 (0.48) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL16986998 0.88 PKM (0.49) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL3970403 0.88 PKM (0.49) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL2443534 0.87 PKM (0.48) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL4129353 0.87 PKM (0.48) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL1958618 0.87 PKM (0.48) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL21963889 0.85 PKM (0.47) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL7309006 0.85 USP2 (0.43) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL15437724 0.85 PKM (0.47) PKMUSP2SMN1; SMN2CYP4F2CYP4A11
SCHEMBL23390562 0.84 NR1H2 (0.42) PKMUSP2SMN1; SMN2CYP4F2CYP4A11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250353854-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN BIOMEA FUSION INC (US) 2025-11-20 US disclosed
WO-2024249950-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN BIOMEA FUSION, INC. (US) 2024-12-05 WO disclosed
WO-2023235618-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN BIOMEA FUSION, INC. (US) 2023-12-07 WO disclosed
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2022-02-15 US disclosed
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors INCYTE CORPORATION (US) 2022-02-15 US disclosed
EP-3626713-B1 CYCLOPROPYLAMINES FOR USE AS LSD1 INHIBITORS INCYTE CORP (US) 2021-09-29 EP disclosed
EP-3626713-B1 CYCLOPROPYLAMINES FOR USE AS LSD1 INHIBITORS INCYTE CORP (US) 2021-09-29 EP disclosed
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-02-04 US disclosed
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS INCYTE CORPORATION 2021-02-04 US disclosed
CN-111454188-A Cyclopropylamines as L SD1inhibitors 因赛特公司 2020-07-28 CN disclosed
US-8071625-B2 E.g., [(1-(2-aminoacetyl)-4-{N-[(3-fluoro-2-methylphenyl)methyl]carbamoyl}(4-piperidyl))methoxy]-N-(4-ethylphenyl)carboxamide; smooth muscle myosin or non-muscle myosin modulator; hypotensive agent; asthma, COPD, bronchoconstrictive disease, glaucoma, pre-menstrual cramps, erectile dysfunction CYTOKINETICS, INC. (US) 2011-12-06 US disclosed
US-8071625-B2 E.g., [(1-(2-aminoacetyl)-4-{N-[(3-fluoro-2-methylphenyl)methyl]carbamoyl}(4-piperidyl))methoxy]-N-(4-ethylphenyl)carboxamide; smooth muscle myosin or non-muscle myosin modulator; hypotensive agent; asthma, COPD, bronchoconstrictive disease, glaucoma, pre-menstrual cramps, erectile dysfunction CYTOKINETICS, INC. (US) 2011-12-06 US disclosed
US-20090264466-A1 Certain Chemical Entities, Compositions and Methods CYTOKINETICS, INC. 2009-10-22 US disclosed
US-20090264466-A1 Certain Chemical Entities, Compositions and Methods CYTOKINETICS, INC. 2009-10-22 US disclosed
US-20090264466-A1 Certain Chemical Entities, Compositions and Methods CYTOKINETICS, INC. 2009-10-22 US disclosed
US-20080194633-A1 Certain chemical entities, compositions, and methods CYTOKINETICS, INC. 2008-08-14 US disclosed
US-20080194633-A1 Certain chemical entities, compositions, and methods CYTOKINETICS, INC. 2008-08-14 US disclosed
US-20080194633-A1 Certain chemical entities, compositions, and methods CYTOKINETICS, INC. 2008-08-14 US disclosed
WO-2008016676-A2 CERTAIN CHEMICAL ENTITIES, COMPOSITIONS, AND METHODS CYTOKINETICS, INCORPORATED (US) 2008-02-07 WO disclosed
WO-2008016676-A2 CERTAIN CHEMICAL ENTITIES, COMPOSITIONS, AND METHODS CYTOKINETICS, INCORPORATED (US) 2008-02-07 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 (5 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-20080194633-A1 Certain chemical entities, compositions, and methods MYLK, MYH2, MYH10 PKM 478/4885USP2 2522/4885SMN1; SMN2 252/4885
US-11247992-B2 Cyclopropylamines as LSD1 inhibitors KDM1B, KDM1A, KDM2A PKM 1859/4885USP2 422/4885SMN1; SMN2 2689/4885
US-20090264466-A1 Certain Chemical Entities, Compositions and Methods MYLK, MYH2, MYH10 PKM 433/4885USP2 2629/4885SMN1; SMN2 262/4885
US-20250353854-A1 FUSED PYRIMIDINE COMPOUNDS AS INHIBITORS OF MENIN MEN1, MLLT1, MSI2 PKM 3271/4885USP2 3835/4885SMN1; SMN2 2354/4885
US-20210032244-A1 CYCLOPROPYLAMINES AS LSD1 INHIBITORS KDM1B, KDM1A, KDM2A PKM 1859/4885USP2 422/4885SMN1; SMN2 2689/4885

“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.