SCHEMBL589519

SCHEMBL589519

CC(O)c1ccc(F)cn1

nearest known ligand 0.57

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
APLNR P35414 2/20 0.57
ESR1 P03372 2/20 0.38
ESR2 Q92731 2/20 0.38
HDAC6 Q9UBN7 1/20 0.38
JAK2 O60674 4/20 0.36
JAK3 P52333 3/20 0.36
HRH1 P35367 1/20 0.36
KCNH2 Q12809 1/20 0.36
FFAR2 O15552 1/20 0.35
TRPA1 O75762 1/20 0.34
NR1I2 O75469 2/20 0.33
TRPV3 Q8NET8 1/20 0.33
MEN1 O00255 1/20 0.33
KMT2A Q03164 1/20 0.33
MAPK1 P28482 1/20 0.33
P2RX3 P56373 1/20 0.32
P2RX2 Q9UBL9 1/20 0.32
KMO O15229 1/20 0.32

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
SCHEMBL29858360 1.00 APLNR (0.57) APLNRESR1ESR2HDAC6JAK2
SCHEMBL25203689 1.00 APLNR (0.57) APLNRESR1ESR2HDAC6JAK2
SCHEMBL1856342 1.00 APLNR (0.57) APLNRESR1ESR2HDAC6JAK2
SCHEMBL3234164 0.85 APLNR (0.52) APLNRKCNH2FFAR2NR1I2MAPK1
SCHEMBL14815592 0.84 APLNR (0.44) APLNR
SCHEMBL179299 0.82 APLNR (0.51) APLNRESR1ESR2HDAC6JAK2
SCHEMBL3234173 0.81 APLNR (0.49) APLNRESR1ESR2HDAC6HRH1
SCHEMBL22506484 0.80 APLNR (0.64) APLNRHDAC6JAK2JAK3KMT2A
SCHEMBL20470117 0.80 APLNR (0.64) APLNRHDAC6JAK2JAK3KMT2A
SCHEMBL20470327 0.80 APLNR (0.64) APLNRHDAC6JAK2JAK3KMT2A

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
US-12545684-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2026-02-10 US disclosed
WO-2025101892-A1 POLY-ADP RIBOSE POLYMERASE (PARP) INHIBITORS AND USES THEREOF Astellas Engineered Small Molecules US, Incorporated (US) 2025-05-15 WO disclosed
US-20240383902-A1 CDK2 INHIBITORS BLUEPRINT MEDICINES CORPORATION 2024-11-21 US disclosed
WO-2024222860-A1 SALT OF MORPHOLINE HETEROCYCLIC COMPOUND, AND PREPARATION METHOD THEREFOR AND USE THEREOF 江苏豪森药业集团有限公司 2024-10-31 WO disclosed
CN-118852146-A Crystal form of morpholine heterocyclic compound, and preparation method and application thereof 江苏豪森药业集团有限公司 2024-10-29 CN disclosed
CN-118176185-A 2- (Aryl-2-yl) morpholine and deuterated derivative thereof, preparation method and application 上海翰森生物医药科技有限公司 2024-06-11 CN disclosed
US-20240174683-A1 MAP4K1 INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2024-05-30 US disclosed
US-11970498-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2024-04-30 US disclosed
US-11932648-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2024-03-19 US disclosed
EP-4288437-A1 MAP4K1 INHIBITORS Bayer Aktiengesellschaft (DE) 2023-12-13 EP disclosed
EP-2069364-A1 NOVEL 5, 7-DISUBSTITUTED [1, 3]THIAZOLO [4, 5-D]PYRIMIDIN-2 (3H)-ONE DERIVATIVES AND THEIR USE IN THERAPY AstraZeneca AB (SE) 2009-06-17 EP disclosed
EP-2069365-A1 NOVEL 5,7-DISUBSTITUTED [1, 3]THIAZOLO [4, 5D]PYRIMIDIN-2 (3H)-AMINE DERIVATIVES AND THEIR USE IN THERAPY AstraZeneca AB (SE) 2009-06-17 EP disclosed
WO-2009016410-A2 CHEMICAL COMPOUNDS 831 ASTRAZENECA AB (SE) 2009-02-05 WO disclosed
WO-2009007753-A2 4- (3-AMINOPYRAZOLE) -PYRIMIDINE DERIVATIVEE AND THEIR USE AS TYROSINE KINASE INHIBITORS FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2009-01-15 WO disclosed
US-20080287437-A1 Pyrazolylaminopyrimidine Derivatives Useful as Tyrosine Kinase Inhibitors ASTRAZENECA AB (SE) 2008-11-20 US disclosed
WO-2008132502-A1 PYRAZOLYL-AMINO-SUBSTITUTED PYRIMIDINES AND THEIR USE FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2008-11-06 WO disclosed
WO-2008117050-A1 PYRAZOLYL-AMINO-SUBSTITUTED PYRAZINES AND THEIR USE FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2008-10-02 WO disclosed
WO-2008039139-A1 NOVEL 5,7-DISUBSTITUTED [1, 3] THIAZOLO [4, 5] PYRIMIDIN-2 (3H)-AMINE DERIVATIVES AND THEIR USE IN THERAPY ASTRAZENECA AB (SE) 2008-04-03 WO disclosed
WO-2008039139-A1 NOVEL 5,7-DISUBSTITUTED [1, 3] THIAZOLO [4, 5] PYRIMIDIN-2 (3H)-AMINE DERIVATIVES AND THEIR USE IN THERAPY ASTRAZENECA AB (SE) 2008-04-03 WO disclosed
WO-2008039138-A1 NOVEL 5, 7-DISUBSTITUTED [1, 3 ] THIAZOLO [4, 5-D] PYRIMIDIN-2 (3H)-ONE DERIVATIVES AND THEIR USE IN THERAPY ASTRAZENECA AB (SE) 2008-04-03 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 (6 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-11932648-B2 CDK2 inhibitors CDK2, CDK20, CDK2AP1 APLNR 4664/4885ESR1 1428/4885ESR2 2253/4885
US-20080287437-A1 Pyrazolylaminopyrimidine Derivatives Useful as Tyrosine Kinase Inhibitors ABL1, FLT3, ERBB2 APLNR 3478/4885ESR1 3445/4885ESR2 2264/4885
US-20240174683-A1 MAP4K1 INHIBITORS MAP3K4, MAP4K4, MAP4K1 APLNR 3263/4885ESR1 1253/4885ESR2 1944/4885
US-11970498-B2 CDK2 inhibitors CDK2, CDK20, CDK2AP1 APLNR 4664/4885ESR1 1428/4885ESR2 2253/4885
US-20240383902-A1 CDK2 INHIBITORS CDK2, CDK20, CDK2AP1 APLNR 4664/4885ESR1 1428/4885ESR2 2253/4885
US-12545684-B2 CDK2 inhibitors CDK2, CDK4, CDK1 APLNR 4594/4885ESR1 1827/4885ESR2 1666/4885

“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.