SCHEMBL5474167

SCHEMBL5474167

CCOC(=O)c1cc(C(F)(F)F)nn1-c1cccc(C#N)c1

nearest known ligand 0.51

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
KLKB1 P03952 13/20 0.51
SCN9A Q15858 1/20 0.48
CARM1 Q86X55 2/20 0.46
ELANE P08246 3/20 0.44
CYP2C9 P11712 1/20 0.43
PLG P00747 1/20 0.42
PRSS1 P07477 1/20 0.42
PRSS2 P07478 1/20 0.42
PRSS3 P35030 1/20 0.42
KDM4E B2RXH2 1/20 0.42
ALDH1A1 P00352 1/20 0.42

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
SCHEMBL2922816 0.90 GRN (0.48) KLKB1SCN9AELANEKDM4EALDH1A1
SCHEMBL21100762 0.88 KLKB1 (0.53) KLKB1CARM1PLGPRSS1PRSS2
SCHEMBL23428812 0.87 KLKB1 (0.51) KLKB1CARM1PLGPRSS1PRSS2
SCHEMBL31067538 0.85 KMT2A (0.51) SCN9AELANEKDM4EALDH1A1
SCHEMBL3833007 0.85 KMT2A (0.51) SCN9AELANEKDM4EALDH1A1
SCHEMBL12361464 0.84 ALDH1A1 (0.53) KLKB1SCN9AKDM4EALDH1A1
SCHEMBL3830194 0.83 KLKB1 (0.63) KLKB1CARM1PLGPRSS1PRSS2
SCHEMBL18630528 0.83 KLKB1 (0.55) KLKB1CARM1PLGPRSS1PRSS2
SCHEMBL20502767 0.83 KLKB1 (0.59) KLKB1SCN9ACARM1KDM4EALDH1A1
SCHEMBL2926900 0.83 ALDH1A1 (0.47) SCN9AELANEKDM4EALDH1A1

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
US-20070060589-A1 Inhibitors of protein arginine methyl transferases BRISTOL-MYERS SQUIBB COMPANY 2007-03-15 US disclosed
WO-2006069155-A2 INHIBITORS OF PROTEIN ARGININE METHYL TRANSFERASES BRISTOL-MYERS SQUIBB COMPANY (US) 2006-06-29 WO disclosed
US-6465656-B2 ACYLATING/ACETYLATING ARYLHYDRAZINE, REACTING HYDROZONOYL HALIDE/SULFATE WITH AMINE BASE TO FORM 1-(3-CYANO)PHENYL-2-(TRIFLUOROACETYL)HYDRAZINE BRISTOL-MYERS SQUIBB PHARMA COMPANY 2002-10-15 US disclosed
EP-1222172-A1 SYNTHESIS OF 1,3,5-TRISUBSTITUTED PYRAZOLES AND INTERMEDIATES THEREFORE Bristol-Myers Squibb Pharma Company (US) 2002-07-17 EP disclosed
US-20020055641-A1 Synthesis of 1,3,5-trisubstituted pyrazoles BRISTOL-MYERS SQUIBB PHARMA COMPANY 2002-05-09 US disclosed
US-6329527-B1 ACYLATING SUBSTITUTEDARYL HYDRAZINE, FORMING DIPOLAR COMPOUND, CONTACTING DIPOLAROPHILE AND SUBJECTING TO OXIDATION, REMOVING PROTECTING GROUP BRISTOL-MYERS SQUIBB PHARMA COMPANY 2001-12-11 US disclosed
WO-2001029006-A1 SYNTHESIS OF 1,3,5-TRISUBSTITUTED PYRAZOLES AND INTERMEDIATES THEREFORE BRISTOL-MYERS SQUIBB PHARMA COMPANY (US) 2001-04-26 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 (2 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-20020055641-A1 Synthesis of 1,3,5-trisubstituted pyrazoles TFPI, SERPINC1, F11 KLKB1 277/4885SCN9A 2844/4885CARM1 3937/4885
US-20070060589-A1 Inhibitors of protein arginine methyl transferases PRMT1, PRMT3, PRMT6 KLKB1 3255/4885SCN9A 4329/4885CARM1 20/4885

“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.