SCHEMBL14924068

SCHEMBL14924068

CC(C)c1ccc(N2CCC(N3CCCC3)CC2)c(F)c1

nearest known ligand 0.46

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
L3MBTL3 Q96JM7 5/20 0.46
L3MBTL1 Q9Y468 4/20 0.46
MBTD1 Q05BQ5 2/20 0.43
CSF1R P07333 1/20 0.42
CDK4 P11802 1/20 0.42
CDK6 Q00534 1/20 0.42
NPY2R P49146 2/20 0.41
ALDH1A1 P00352 2/20 0.40
SMN1; SMN2 Q16637 1/20 0.40
HRH3 Q9Y5N1 2/20 0.39
MAPT P10636 2/20 0.39
AXL P30530 1/20 0.39
GAA P10253 1/20 0.39
HPGD P15428 1/20 0.38
TSHR P16473 1/20 0.38
CCR4 P51679 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
SCHEMBL14924049 0.99 L3MBTL3 (0.45) L3MBTL3L3MBTL1MBTD1CSF1RCDK4
SCHEMBL13467936 0.91 L3MBTL3 (0.43) L3MBTL3L3MBTL1MBTD1CSF1RCDK4
SCHEMBL14924073 0.88 KDM2B (0.48) CSF1RCDK4CDK6ALDH1A1SMN1; SMN2
SCHEMBL17660584 0.87 ABCB1 (0.47) MAPTTSHR
SCHEMBL14200383 0.86 L3MBTL3 (0.46) L3MBTL3L3MBTL1MBTD1NPY2RHRH3
SCHEMBL14924052 0.86 NPY2R (0.52) L3MBTL3L3MBTL1MBTD1NPY2RALDH1A1
SCHEMBL12160700 0.85 ALDH1A1 (0.53) ALDH1A1SMN1; SMN2MAPTGAAHPGD
SCHEMBL22860583 0.84 PIK3CD (0.42) CSF1RCDK4CDK6HRH3
SCHEMBL14410284 0.83 L3MBTL3 (0.46) L3MBTL3L3MBTL1MBTD1NPY2RALDH1A1
SCHEMBL16249197 0.83 ALDH1A1 (0.51) ALDH1A1SMN1; SMN2MAPTGAAHPGD

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230062022-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS NUVATION BIO INC (US) 2023-03-02 US disclosed
US-11174252-B2 Heterocyclic compounds as kinase inhibitors NUVATION BIO INC. (US) 2021-11-16 US disclosed
US-20190248774-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS SAGARD HOLDINGS MANAGER LP, AS ADMINISTRATIVE AGENT (CA) 2019-08-15 US disclosed
US-RE46511-E1 Fused pyrimidine derivatives for inhibition of tyrosine kinase activity HANMI SCIENCE CO., LTD. (KR) 2017-08-15 US disclosed
US-RE46511-E1 Fused pyrimidine derivatives for inhibition of tyrosine kinase activity HANMI SCIENCE CO., LTD. (KR) 2017-08-15 US disclosed
US-20160229868-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY HANMI SCIENCE CO., LTD (KR) 2016-08-11 US disclosed
US-9345719-B2 Fused pyrimidine derivatives for inhibition of tyrosine kinase activity HANMI SCIENCE CO., LTD. (KR) 2016-05-24 US disclosed
US-8957065-B2 Fused pyrimidine derivatives for inhibition of tyrosine kinase activity HANMI SCIENCE CO., LTD (KR) 2015-02-17 US disclosed
US-20150045324-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY HANMI SCIENCE CO., LTD (KR) 2015-02-12 US disclosed
US-20130116213-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY HANMI SCIENCE CO., LTD. (KR) 2013-05-09 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 (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-20160229868-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY LCK, LTK, FYN L3MBTL3 3429/4885L3MBTL1 2596/4885MBTD1 754/4885
US-11174252-B2 Heterocyclic compounds as kinase inhibitors CDK6, CDK4, CDK9 L3MBTL3 3021/4885L3MBTL1 2902/4885MBTD1 1827/4885
US-20190248774-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS CDK4, CDK6, CDK8 L3MBTL3 1705/4885L3MBTL1 1563/4885MBTD1 1365/4885
US-20230062022-A1 HETEROCYCLIC COMPOUNDS AS KINASE INHIBITORS CDK4, CDK6, CDK8 L3MBTL3 1705/4885L3MBTL1 1563/4885MBTD1 1365/4885
US-20150045324-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY LCK, FYN, TYK2 L3MBTL3 3628/4885L3MBTL1 2790/4885MBTD1 799/4885
US-20130116213-A1 NOVEL FUSED PYRIMIDINE DERIVATIVES FOR INHIBITION OF TYROSINE KINASE ACTIVITY LCK, FYN, TYK2 L3MBTL3 3628/4885L3MBTL1 2790/4885MBTD1 799/4885

“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.