SCHEMBL6498768

SCHEMBL6498768

CCC(=O)c1ccc(N=C=O)cc1

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.48
MAPT P10636 3/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
CYP3A4 P08684 2/20 0.48
TSHR P16473 1/20 0.48
RAB9A P51151 4/20 0.40
PGR P06401 1/20 0.40
TRPA1 O75762 1/20 0.39
ATM Q13315 1/20 0.39
KMT2A Q03164 2/20 0.37
NPC1 O15118 2/20 0.37
MEN1 O00255 1/20 0.37
HSD17B3 P37058 2/20 0.37
GABRA1 P14867 1/20 0.37
GABRB2 P47870 1/20 0.37
MAPK1 P28482 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
CYP1A2 P05177 1/20 0.37
ALDH1A1 P00352 2/20 0.36
GAA P10253 1/20 0.36

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
SCHEMBL3631791 0.85 HSD17B3 (0.56) SMN1; SMN2L3MBTL1CYP3A4TSHRNPC1
SCHEMBL13664653 0.83 HSD17B10 (0.47) SMN1; SMN2MAPTL3MBTL1RAB9APGR
SCHEMBL9420576 0.81 NPC1 (0.48) MAPTL3MBTL1CYP3A4TSHRRAB9A
SCHEMBL2763360 0.80 CYP3A4 (0.44) SMN1; SMN2MAPTL3MBTL1CYP3A4TSHR
SCHEMBL1878539 0.79 CYP3A4 (0.57) MAPTL3MBTL1CYP3A4TSHRRAB9A
SCHEMBL27661229 0.79 GABRA1 (0.41) SMN1; SMN2MAPTL3MBTL1CYP3A4TSHR
SCHEMBL8051337 0.78 SMN1; SMN2 (0.70) SMN1; SMN2MAPTL3MBTL1RAB9APGR
SCHEMBL219763 0.78 NOS3 (0.55) SMN1; SMN2MAPTL3MBTL1CYP3A4TSHR
SCHEMBL13455429 0.78 SMN1; SMN2 (0.53) SMN1; SMN2MAPTL3MBTL1TSHRRAB9A
SCHEMBL308386 0.77 CYP3A4 (0.52) MAPTCYP3A4TSHRTRPA1MAPK1

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-6956053-B2 Pyrazole derivatives and their use as gastrin and cholecystokin receptor ligands THE JAMES BLACK FOUNDATION LIMITED (GB) 2005-10-18 US disclosed
US-20030207874-A1 Pyrazole derivatives and their use as gastrin and cholecystokin receptor ligands JAMES BLACK FOUNDATION LIMITED, THE (GB) 2003-11-06 US disclosed
WO-2001090078-A1 PYRAZOLE DERIVATIVES AND THEIR USE AS GASTRIN AND CHOLECYSTOKIN IN RECEPTOR LIGANDS JAMES BLACK FOUNDATION LIMITED (GB) 2001-11-29 WO disclosed
US-4977272-A Radiation absorbers THE STANDARD OIL COMPANY (US) 1990-12-11 US disclosed
US-4868061-A ADDITION POLYMERS, ULTRAVIOLET RADIATION STABILIZERS THE STANDARD OIL COMPANY (US) 1989-09-19 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-20030207874-A1 Pyrazole derivatives and their use as gastrin and cholecystokin receptor ligands CCKBR, GRPR, CCKAR SMN1; SMN2 4823/4885MAPT 4713/4885L3MBTL1 4487/4885

“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.