SCHEMBL3249696

SCHEMBL3249696

N[C@@H]1CCC(N2CCC(NC(=O)OCc3ccccc3)C2=O)C(NC(=O)O)C1

nearest known ligand 0.48

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
PREP P48147 2/20 0.45
CASP3 P42574 1/20 0.44
CPB1 P15086 2/20 0.44
CTSK P43235 2/20 0.43
NAAA Q02083 2/20 0.43
TSHR P16473 1/20 0.43
ALDH1A1 P00352 1/20 0.42
GAA P10253 1/20 0.42
CASP1 P29466 2/20 0.42
CTSL P07711 1/20 0.41
CTSB P07858 1/20 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
SCHEMBL3945925 1.00 PREP (0.45) PREPCASP3CPB1CTSKNAAA
SCHEMBL3249694 1.00 PREP (0.45) PREPCASP3CPB1CTSKNAAA
SCHEMBL3440819 0.87 ALDH1A1 (0.46) PREPCASP3CPB1CTSKNAAA
SCHEMBL3252081 0.87 PREP (0.48) PREPCASP3CPB1CTSKNAAA
SCHEMBL3751199 0.87 PREP (0.48) PREPCASP3CPB1CTSKNAAA
SCHEMBL3751193 0.87 PREP (0.48) PREPCASP3CPB1CTSKNAAA
SCHEMBL3252082 0.87 PREP (0.48) PREPCASP3CPB1CTSKNAAA
SCHEMBL27647294 0.85 CPB1 (0.46) PREPCASP3CPB1CTSKNAAA
SCHEMBL27647296 0.85 CPB1 (0.46) PREPCASP3CPB1CTSKNAAA
SCHEMBL3738297 0.85 CPB1 (0.54) PREPCASP3CPB1CTSKTSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2049519-B9 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2010-12-29 EP disclosed
EP-2194051-A1 Process for preparing compounds useful as intermediates for the preparation of modulators of chemokine receptor activity Bristol-Myers Squibb Company (US) 2010-06-09 EP disclosed
EP-2049519-B1 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2010-05-12 EP disclosed
US-20100113489-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY, CRYSTALLINE FORMS AND PROCESS BRISTOL-MYERS SQUIBB COMPANY 2010-05-06 US disclosed
US-7687508-B2 Cyclic derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY (US) 2010-03-30 US disclosed
US-7629351-B2 N-((1R,2S,5R)-5-(tert-butylamino)-2-((S)-2-oxo-3-(6-(trifluoromethyl)quinazolin-4-ylamino) pyrrolidin-1-yl)cyclohexyl)acetamide and other modulators of chemokine receptor activity, crystalline forms and process BRISTOL-MYERS SQUIBB COMPANY (US) 2009-12-08 US disclosed
US-20080027084-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CRYSTALLINE FORMS AND PROCESS BRISTOL-MYERS SQUIBB COMPANY 2008-01-31 US disclosed
US-20080027080-A1 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY 2008-01-31 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-20080027084-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CRYSTALLINE FORMS AND PROCESS ACKR3, CCR1, CXCR1 PREP 1946/4885CASP3 1476/4885CPB1 1105/4885
US-20080027080-A1 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CCR5, CXCR4, CCR7 PREP 1679/4885CASP3 3061/4885CPB1 1115/4885
US-20100113489-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY, CRYSTALLINE FORMS AND PROCESS ACKR3, CCR1, CCR2 PREP 1931/4885CASP3 1702/4885CPB1 1107/4885

“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.