SCHEMBL5030435

SCHEMBL5030435

CC(C)N(C)C1CCC(NC(=O)CNC(=O)OCc2ccccc2)CC1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.67
CCR2 P41597 2/20 0.54
GAA P10253 1/20 0.53
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
TSHR P16473 2/20 0.51
CYP3A4 P08684 2/20 0.46
CTSL P07711 1/20 0.46
CTSB P07858 1/20 0.46
CTSS P25774 1/20 0.46
CTSK P43235 1/20 0.46
LIPG Q9Y5X9 5/20 0.44
OPRK1 P41145 1/20 0.44
KDM1A O60341 1/20 0.44
RCOR1 Q9UKL0 1/20 0.44
LIPC P11150 1/20 0.43
KCNH2 Q12809 2/20 0.43
EPHX1 P07099 1/20 0.43
DPP4 P27487 1/20 0.43
DPP7 Q9UHL4 1/20 0.43

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
SCHEMBL5030442 1.00 ALDH1A1 (0.67) ALDH1A1CCR2GAAMEN1KMT2A
SCHEMBL8717361 0.86 ALDH1A1 (0.87) ALDH1A1GAAMEN1KMT2ATSHR
SCHEMBL5029286 0.84 ALDH1A1 (0.52) ALDH1A1CCR2MEN1KMT2ATSHR
SCHEMBL5033696 0.82 CCR2 (0.61) ALDH1A1CCR2TSHRCYP3A4KDM1A
SCHEMBL5033692 0.82 CCR2 (0.61) ALDH1A1CCR2TSHRCYP3A4KDM1A
SCHEMBL5713028 0.81 ALDH1A1 (1.00) ALDH1A1GAAMEN1KMT2ATSHR
Trifluoroacetic Acid SCHEMBL5030519 0.80 CCR2 (0.53) ALDH1A1CCR2TSHRCYP3A4KCNH2
SCHEMBL16055815 0.77 ALDH1A1 (0.69) ALDH1A1GAAMEN1KMT2ATSHR
SCHEMBL8326426 0.77 ALDH1A1 (0.69) ALDH1A1GAAMEN1KMT2ATSHR
SCHEMBL10325767 0.77 ALDH1A1 (0.69) ALDH1A1GAAMEN1KMT2ATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7378409-B2 Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY (US) 2008-05-27 US disclosed
EP-1656138-A4 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL MYERS SQUIBB CO (US) 2007-04-18 EP disclosed
EP-1656138-A2 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY Bristol-Myers Squibb Company (US) 2006-05-17 EP disclosed
WO-2005020899-A2 SUBSTITUTED CYCLOALKYAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY (US) 2005-03-10 WO disclosed
US-20050054626-A1 Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY 2005-03-10 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 (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-20050054626-A1 Substituted cycloalkylamine derivatives as modulators of chemokine receptor activity CCL11, CCR1, CCR2 ALDH1A1 827/4885CCR2 3/4885GAA 4005/4885

“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.