SCHEMBL4574192

SCHEMBL4574192

CCOC(=O)c1cc(-c2ccccc2)n(N)c1C

nearest known ligand 0.67

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.67
HPGD P15428 2/20 0.67
TSHR P16473 2/20 0.67
SMN1; SMN2 Q16637 2/20 0.67
NPSR1 Q6W5P4 1/20 0.64
MEN1 O00255 2/20 0.62
GLA P06280 2/20 0.62
KMT2A Q03164 2/20 0.62
GAA P10253 2/20 0.58
TP53 P04637 6/20 0.57
LMNA P02545 6/20 0.55
MAPT P10636 4/20 0.54
POLB P06746 2/20 0.54
RAB9A P51151 2/20 0.52
ALOX15 P16050 1/20 0.52
HSD17B10 Q99714 1/20 0.52
NPC1 O15118 1/20 0.52
MAPK1 P28482 1/20 0.52

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
SCHEMBL2213963 0.84 NPSR1 (0.70) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL5922348 0.82 LMNA (0.69) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL14276075 0.80 ALDH1A1 (0.63) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL7168904 0.79 CHRNA7 (0.60) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL4574483 0.78 ALDH1A1 (0.49) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL1156108 0.78 ALDH1A1 (0.64) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL7166012 0.77 LMNA (0.66) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL31650801 0.77 ALDH1A1 (0.60) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL7165586 0.77 TP53 (0.74) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1
SCHEMBL5922342 0.77 CHRNA7 (0.72) ALDH1A1HPGDTSHRSMN1; SMN2NPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7319084-B2 Catalysts containing N-pyrrolyl substituted nitrogen donors E.I. DU PONT DE NEMOURS AND COMPANY (US) 2008-01-15 US disclosed
US-20060178490-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors E. I. DU PONT DE NEMOURS AND COMPANY 2006-08-10 US disclosed
US-20050054856-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors EASTMAN CHEMICAL COMPANY (US) 2005-03-10 US disclosed
US-6825356-B2 REMAINING DONOR ATOMS OF THE LIGAND ARE SELECTED FROM THE GROUP CONSISTING OF C, N, P, AS, O, S, AND SE EASTMAN CHEMICAL COMPANY 2004-11-30 US disclosed
US-20030225228-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors EASTMAN CHEMICAL COMPANY 2003-12-04 US disclosed
US-20030195110-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors E. I. DU PONT DE NEMOURS AND COMPANY 2003-10-16 US disclosed
US-6559091-B1 Metal complex ligated by a monodentate, bidentate, tridentate, or tetradentate ligand, wherein at least one of the donor atoms of the ligand is a nitrogen atom substituted by a 1-pyrrolyl or substituted 1- pyrrolyl group EASTMAN CHEMICAL COMPANY 2003-05-06 US disclosed
US-6545108-B1 Ti, Zr, Hf, Cr, Mo, W, V, Nb, or Ta complex of a monodentate dianionic ligand in which a nitrogen atom is substituted by a 1-pyrrolyl and the remaining donor atoms are N, P, As, O, S, or Se EASTMAN CHEMICAL COMPANY 2003-04-08 US disclosed
EP-1278784-A2 CATALYSTS CONTAINING N-PYRROLYL SUBSTITUTED NITROGEN DONORS EASTMAN CHEMICAL COMPANY (US) 2003-01-29 EP disclosed
EP-1192189-A2 CATALYSTS CONTAINING N-PYRROLYL SUBSTITUTED NITROGEN DONORS EASTMAN CHEMICAL COMPANY (US) 2002-04-03 EP disclosed
WO-2001083571-A2 CATALYSTS CONTAINING N-PYRROLYL SUBSTITUTED NITROGEN DONORS EASTMAN CHEMICAL COMPANY (US) 2001-11-08 WO disclosed
WO-2000050470-A2 CATALYSTS CONTAINING N-PYRROLYL SUBSTITUTED NITROGEN DONORS EASTMAN CHEMICAL COMPANY (US) 2000-08-31 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-20060178490-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors NCL, NSFL1C, NCLN ALDH1A1 3786/4885HPGD 79/4885TSHR 4856/4885
US-20050054856-A1 Catalysts containing N-pyrrolyl substituted nitrogen donors NCL, NSFL1C, NCLN ALDH1A1 3786/4885HPGD 79/4885TSHR 4856/4885

“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.