SCHEMBL3604756

SCHEMBL3604756

CCCCN(CCCC)CCS(=O)(=O)N(CC(=O)OCc1ccccc1)c1ccc(C(=O)c2c(-c3ccccc3)c(OC)c3ccccn23)cc1OC

nearest known ligand 0.33

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.32
ACHE P22303 3/20 0.31
BCHE P06276 2/20 0.31
MAPT P10636 1/20 0.31
NPC1 O15118 1/20 0.31
GAA P10253 1/20 0.31
ATM Q13315 1/20 0.31
RXFP1 Q9HBX9 1/20 0.31
KMT2A Q03164 1/20 0.30
MARK4 Q96L34 1/20 0.30
LMNA P02545 1/20 0.30

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
Hydrochloric Acid SCHEMBL3606134 0.99 SMN1; SMN2 (0.31) SMN1; SMN2ACHEBCHEMAPTNPC1
SCHEMBL3597898 0.92 NPC1 (0.35) SMN1; SMN2ACHEBCHEMAPTNPC1
SCHEMBL3597180 0.91 MAPT (0.34) ACHEBCHEMAPTNPC1GAA
SCHEMBL3601517 0.82 NPC1 (0.36) SMN1; SMN2MAPTNPC1GAAATM
SCHEMBL3592666 0.82 NPC1 (0.36) SMN1; SMN2MAPTNPC1GAAATM
SCHEMBL3595468 0.80 MAPT (0.34) ACHEBCHEMAPTNPC1GAA
Hydrochloric Acid SCHEMBL3601670 0.76 MAPT (0.36) SMN1; SMN2ACHEMAPTNPC1GAA
SCHEMBL3593134 0.76 MAPT (0.40) SMN1; SMN2MAPTNPC1GAAATM
SCHEMBL3598724 0.73 NPC1 (0.39) SMN1; SMN2MAPTNPC1GAAATM
Hydrochloric Acid SCHEMBL3596333 0.72 NPC1 (0.39) SMN1; SMN2MAPTNPC1GAAATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7803811-B2 1,2,3-substituted indolizine derivatives, inhibitors of FGFs, method for preparing them and pharmaceutical compositions containing them SANOFI-AVENTIS (FR) 2010-09-28 US disclosed
US-20090023770-A1 Novel 1,2,3-Substituted Indolizine Derivatives, Inhibitors of FGFs, Method for Preparing Them and Pharmaceutical Compositions Containing Them SANOFI-AVENTIS (FR) 2009-01-22 US disclosed
US-7442708-B2 1,2,3-substituted indolizine derivatives, inhibitors of fgfs, method for making same and pharmaceutical compositions containing same SANOFI-AVENTIS (FR) 2008-10-28 US disclosed
US-20050203126-A1 Novel 1,2,3-substituted indolizine derivatives, inhibitors of fgfs, method for making same and pharmaceutical compositions containing same SANOFI (FR) 2005-09-15 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 (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-20050203126-A1 Novel 1,2,3-substituted indolizine derivatives, inhibitors of fgfs, method for making same and pharmaceutical compositions containing same FGFR3, FGFR1, NTRK3 SMN1; SMN2 3745/4885ACHE 4222/4885BCHE 1443/4885
US-20090023770-A1 Novel 1,2,3-Substituted Indolizine Derivatives, Inhibitors of FGFs, Method for Preparing Them and Pharmaceutical Compositions Containing Them FGF2, FGF1, FGFR1 SMN1; SMN2 4602/4885ACHE 4333/4885BCHE 3282/4885

“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.