SCHEMBL2402887

SCHEMBL2402887

Nc1c(OCc2ccccc2)nc2cccnc2c1O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
L3MBTL1 Q9Y468 4/20 0.48
LTA4H P09960 1/20 0.46
MAPK14 Q16539 1/20 0.46
EGLN1 Q9GZT9 1/20 0.44
CYP3A4 P08684 3/20 0.42
PDE5A O76074 1/20 0.42
ATP4A P20648 1/20 0.41
ATP4B P51164 1/20 0.41
SGMS2 Q8NHU3 1/20 0.41
MGMT P16455 4/20 0.41
KDM4E B2RXH2 3/20 0.41
LMNA P02545 3/20 0.41
TSHR P16473 2/20 0.41
CDK1 P06493 2/20 0.41
CCNB1 P14635 2/20 0.41
CCNA2 P20248 2/20 0.41
CDK2 P24941 2/20 0.41
CCNA1 P78396 2/20 0.41
CYP1A2 P05177 2/20 0.41
CYP2C19 P33261 2/20 0.41

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
SCHEMBL1775713 0.87 L3MBTL1 (0.51) L3MBTL1LTA4HMAPK14EGLN1CYP3A4
SCHEMBL2400897 0.83 L3MBTL1 (0.53) L3MBTL1CYP3A4PDE5AMGMTKDM4E
SCHEMBL312573 0.79 MGMT (0.53) L3MBTL1EGLN1MGMTLMNAPIN1
SCHEMBL311056 0.76 MGMT (0.59) L3MBTL1LTA4HMAPK14MGMTLMNA
SCHEMBL1232862 0.75 L3MBTL1 (0.57) L3MBTL1LTA4HMAPK14CYP3A4PDE5A
SCHEMBL2399974 0.72 KDM4E (0.49) L3MBTL1LTA4HMAPK14EGLN1CYP3A4
SCHEMBL312251 0.72 CYP3A4 (0.49) L3MBTL1LTA4HMAPK14CYP3A4PDE5A
SCHEMBL2400247 0.72 L3MBTL1 (0.47) L3MBTL1LTA4HMAPK14EGLN1CYP3A4
SCHEMBL13313402 0.71 L3MBTL1 (0.49) L3MBTL1LTA4HMAPK14CYP3A4PDE5A
SCHEMBL16852229 0.71 MGMT (0.64) L3MBTL1LTA4HMAPK14CYP3A4PDE5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8378102-B2 Oxime and hydroxylamine substituted thiazolo[4,5-c] ring compounds and methods 3M INNOVATIVE PROPERTIES COMPANY (US) 2013-02-19 US disclosed
US-8026366-B2 Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-09-27 US disclosed
US-20100240693-A1 Oxime and Hydroxylamine Substituted Thiazolo [4,5-C] Ring Compounds and Methods COLEY PHARMACEUTICAL GROUP, INC (US) 2010-09-23 US disclosed
EP-1877056-A2 OXIME AND HYDROXYLAMINE SUBSTITUTED THIAZOLOÝ4,5-C¨RING COMPOUNDS AND METHODS Coley Pharmaceutical Group, Inc. (US) 2008-01-16 EP disclosed
WO-2007120121-A2 OXIME AND HYDROXYLAMINE SUBSTITUTED THIAZOLO[4,5-C] RING COMPOUNDS AND METHODS COLEY PHARMACEUTICAL GROUP, INC. (US) 2007-10-25 WO disclosed
US-20070208052-A1 Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY 2007-09-06 US disclosed
WO-2006009826-A1 ARYLOXY AND ARYLALKYLENEOXY SUBSTITUTED THIAZOLOQUINOLINES AND THIAZOLONAPHTHYRIDINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-01-26 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-20070208052-A1 Aryloxy and arylalkyleneoxy substituted thiazoloquinolines and thiazolonaphthyridines IL2, TSLP, IFNG L3MBTL1 2999/4885LTA4H 448/4885MAPK14 1120/4885
US-20100240693-A1 Oxime and Hydroxylamine Substituted Thiazolo [4,5-C] Ring Compounds and Methods IL4, IL2, TH L3MBTL1 3690/4885LTA4H 626/4885MAPK14 976/4885

“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.