SCHEMBL22166531

SCHEMBL22166531

CCCCCCCC(=O)N(C)CCC(C)(C)C

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ EPHX2 P34913 2/20 0.53
▸ CNR1 P21554 1/20 0.45
▸ KDM5A P29375 3/20 0.44
▸ KDM4C Q9H3R0 2/20 0.44
▸ PHF8 Q9UPP1 1/20 0.44
▸ ALDH1A1 P00352 3/20 0.44
▸ CES2 O00748 3/20 0.42
▸ CES1 P23141 3/20 0.42
▸ KDM5C P41229 1/20 0.41
▸ KDM5B Q9UGL1 1/20 0.41
▸ DNM1 Q05193 2/20 0.41
▸ PPARG P37231 5/20 0.41
▸ PPARD Q03181 5/20 0.41
▸ PPARA Q07869 5/20 0.41
▸ HDAC11 Q96DB2 4/20 0.41
▸ TSHR P16473 3/20 0.41
▸ GPR84 Q9NQS5 3/20 0.41
▸ TLR2 O60603 2/20 0.41
▸ TDP1 Q9NUW8 2/20 0.41
▸ FABP4 P15090 2/20 0.41

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
SCHEMBL22166535 1.00 EPHX2 (0.53) EPHX2CNR1KDM5AKDM4CPHF8
SCHEMBL22021691 0.98 EPHX2 (0.50) EPHX2CNR1KDM5AKDM4CPHF8
SCHEMBL22021680 0.89 EPHX2 (0.41) EPHX2KDM5AKDM4CPHF8
SCHEMBL22021685 0.89 EPHX2 (0.41) EPHX2KDM5AKDM4CPHF8
SCHEMBL22021658 0.89 EPHX2 (0.41) EPHX2KDM5AKDM4CPHF8
SCHEMBL21456131 0.86 CYP4F2 (0.42) EPHX2CNR1KDM5AKDM4CPHF8
SCHEMBL21376559 0.85 EPHX2 (0.36) EPHX2CNR1ALDH1A1CES2CES1
SCHEMBL22021679 0.85 EPHX2 (0.36) EPHX2CNR1KDM5AKDM4CPHF8
SCHEMBL22021659 0.85 EPHX2 (0.39) EPHX2CNR1KDM5AKDM4CPHF8
SCHEMBL7939776 0.85 EPHX2 (0.62) EPHX2CNR1KDM5AKDM4CPHF8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11642342-B2 Combinations of estrogen receptor degraders and cyclin-dependent kinase inhibitors for treating cancer Accutar Biotechnology (US) 2023-05-09 — — US disclosed
US-20210213012-A1 COMBINATIONS OF ESTROGEN RECEPTOR DEGRADERS AND CYCLIN-DEPENDENT KINASE INHIBITORS FOR TREATING CANCER ACCUTAR BIOTECHNOLOGY INC. 2021-07-15 — — US disclosed
US-10696659-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ACCUTAR BIOTECHNOLOGY INC. (US) 2020-06-30 — — 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 (3 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-20210213012-A1 COMBINATIONS OF ESTROGEN RECEPTOR DEGRADERS AND CYCLIN-DEPENDENT KINASE INHIBITORS FOR TREATING CANCER CDK3, CDK4, CDK1 EPHX2 1763/4885CNR1 844/4885KDM5A 790/4885
US-11642342-B2 Combinations of estrogen receptor degraders and cyclin-dependent kinase inhibitors for treating cancer CDK3, CDK4, CDK1 EPHX2 1763/4885CNR1 844/4885KDM5A 790/4885
US-10696659-B2 Compounds having estrogen receptor alpha degradation activity and uses thereof ESR2, ESRRG, ESR1 EPHX2 896/4885CNR1 645/4885KDM5A 2158/4885

“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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