SCHEMBL6558543

SCHEMBL6558543

CC(C)Sc1ccc(F)cc1[N+](=O)[O-]

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PDE7A Q13946 3/20 0.54
▸ TDP1 Q9NUW8 2/20 0.53
▸ ATM Q13315 1/20 0.53
▸ TXNRD1 Q16881 1/20 0.42
▸ TXNRD3 Q86VQ6 1/20 0.42
▸ TXNRD2 Q9NNW7 1/20 0.42
▸ USP10 Q14694 1/20 0.42
▸ USP7 Q93009 1/20 0.42
▸ USP47 Q96K76 1/20 0.42
▸ ALDH1A1 P00352 4/20 0.40
▸ KMT2A Q03164 1/20 0.40
▸ HSPB1 P04792 2/20 0.38
▸ IDO1 P14902 1/20 0.38
▸ PDE4B Q07343 1/20 0.37
▸ PDE4D Q08499 1/20 0.37
▸ PDE7B Q9NP56 1/20 0.37
▸ HTT P42858 1/20 0.36
▸ MAPT P10636 3/20 0.36
▸ MAPK1 P28482 2/20 0.36
▸ L3MBTL1 Q9Y468 1/20 0.36

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
SCHEMBL2061399 0.90 ATM (0.58) PDE7ATDP1ATMTXNRD1TXNRD3
SCHEMBL10651245 0.84 ALDH1A1 (0.56) PDE7ATDP1ATMUSP10USP7
SCHEMBL282648 0.81 TSHR (0.56) TDP1TXNRD1TXNRD3TXNRD2ALDH1A1
SCHEMBL3874156 0.81 PDE7A (0.58) PDE7ATDP1ATMTXNRD1TXNRD3
SCHEMBL6556635 0.80 PDE7A (0.57) PDE7AUSP7ALDH1A1KMT2APDE4B
SCHEMBL11432656 0.80 ALDH1A1 (0.54) PDE7ATDP1TXNRD1TXNRD3TXNRD2
SCHEMBL1026140 0.80 TXNRD1 (0.42) PDE7ATXNRD1TXNRD3TXNRD2ALDH1A1
SCHEMBL10651192 0.78 MAPT (0.49) PDE7ATDP1ATMUSP10USP7
SCHEMBL14866332 0.78 ALDH1A1 (0.49) ALDH1A1KMT2AHTTMAPTMAPK1
SCHEMBL5913415 0.78 ALDH1A1 (0.57) TDP1TXNRD1TXNRD3TXNRD2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0976725-B1 Process for the continuous preparation of amino-halogenophenyl alkyl thioethers BAYER CHEMICALS AG (DE) 2004-03-03 — — EP claimed
US-6077974-A Process for the continuous preparation of amino-halo-genophenyl alkyl thioethers BAYER AKTIENGESELLSCHAFT (DE) 2000-06-20 — — US claimed
EP-0976725-A2 Process for the continuous preparation of amino-halogenophenyl alkyl thioethers Bayer Aktiengesellschaft (DE) 2000-02-02 — — EP claimed
US-20180111905-A1 N2-(2-METHOXYPHENYL)PYRIMIDINE DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION FOR CANCER PREVENTION OR TREATMENT CONTAINING SAME AS ACTIVE INGREDIENT KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2018-04-26 — — US disclosed
EP-0976725-B1 Process for the continuous preparation of amino-halogenophenyl alkyl thioethers BAYER CHEMICALS AG (DE) 2004-03-03 — — EP disclosed
US-6077974-A Process for the continuous preparation of amino-halo-genophenyl alkyl thioethers BAYER AKTIENGESELLSCHAFT (DE) 2000-06-20 — — US disclosed
EP-0976725-A2 Process for the continuous preparation of amino-halogenophenyl alkyl thioethers Bayer Aktiengesellschaft (DE) 2000-02-02 — — EP 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 (1 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-20180111905-A1 N2-(2-METHOXYPHENYL)PYRIMIDINE DERIVATIVE, METHOD FOR PREPARING SAME, AND PHARMACEUTICAL COMPOSITION FOR CANCER PREVENTION OR TREATMENT CONTAINING SAME AS ACTIVE INGREDIENT ALK, NPM1, EML4 PDE7A 4052/4885TDP1 1272/4885ATM 1285/4885

“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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