SCHEMBL1840892

SCHEMBL1840892

CC(C)(C)OC(=O)N[C@@H]1CC[C@H](N2CC[C@H](NC(=O)OCc3ccccc3)C2=O)[C@H](C(N)=O)C1

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.48
KMT2A Q03164 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
ALDH1A1 P00352 1/20 0.43
GAA P10253 1/20 0.43
PREP P48147 2/20 0.42
DPP4 P27487 2/20 0.42
KCNH2 Q12809 2/20 0.42
DPP7 Q9UHL4 2/20 0.42
CPB1 P15086 1/20 0.41
CTSL P07711 1/20 0.41
CTSB P07858 1/20 0.41
CTSK P43235 1/20 0.41
TLR4 O00206 1/20 0.41
DRD2 P14416 1/20 0.40
CASP3 P42574 1/20 0.40

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
SCHEMBL1840896 1.00 TSHR (0.48) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3736738 0.93 ALDH1A1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3736739 0.93 ALDH1A1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL1843571 0.93 ALDH1A1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL1843570 0.93 ALDH1A1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3744222 0.92 CPB1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3732889 0.92 CPB1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3744220 0.92 CPB1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL27667819 0.92 CPB1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA
SCHEMBL3732888 0.92 CPB1 (0.47) TSHRKMT2AL3MBTL1ALDH1A1GAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8049019-B2 Substituted pyrrolidine-2-one compounds BRISTOL-MYERS SQUIBB COMPANY (US) 2011-11-01 US disclosed
EP-2194051-B1 Process for preparing compounds useful as intermediates for the preparation of modulators of chemokine receptor activity BRISTOL MYERS SQUIBB CO (US) 2011-08-31 EP disclosed
EP-2046779-B1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY, CRYSTALLINE FORMS AND PROCESS BRISTOL MYERS SQUIBB CO (US) 2011-05-18 EP disclosed
EP-2049519-B9 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2010-12-29 EP disclosed
EP-2049477-B1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY, CRYSTALLINE FORMS AND PROCESS BRISTOL MYERS SQUIBB CO (US) 2010-06-23 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-2184283-A1 Process for preparing compounds useful as intermediates for the preparation of modulators of chemokine receptor activity Bristol-Myers Squibb Company (US) 2010-05-12 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-7671062-B2 Modulators of chemokine receptor activity, crystalline forms and process BRISTOL-MYERS SQUIBB COMPANY (US) 2010-03-02 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-20080027080-A1 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY 2008-01-31 US disclosed
US-20080027083-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CRYSTALLINE FORMS AND PROCESS BRISTOL-MYERS SQUIBB COMPANY 2008-01-31 US disclosed
US-20080027084-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CRYSTALLINE FORMS AND PROCESS 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 (4 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 TSHR 113/4885KMT2A 3326/4885L3MBTL1 3349/4885
US-20080027083-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CRYSTALLINE FORMS AND PROCESS ACKR3, CCR1, CCR2 TSHR 275/4885KMT2A 3030/4885L3MBTL1 3481/4885
US-20080027080-A1 CYCLIC DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY CCR5, CXCR4, CCR7 TSHR 838/4885KMT2A 4228/4885L3MBTL1 4577/4885
US-20100113489-A1 MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY, CRYSTALLINE FORMS AND PROCESS ACKR3, CCR1, CCR2 TSHR 111/4885KMT2A 3181/4885L3MBTL1 3807/4885

“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.