SCHEMBL1895460

SCHEMBL1895460

CC(C)(O)Cn1cnc2c(Cl)nc3ccccc3c21

nearest known ligand 0.73

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
TLR7 Q9NYK1 15/20 0.73
NUDT1 P36639 2/20 0.46
LMNA P02545 1/20 0.46
POLB P06746 1/20 0.46
HRH2 P25021 1/20 0.46
ADRA1D P25100 1/20 0.46
HTR2A P28223 1/20 0.46
ADORA2A P29274 1/20 0.46
ADRA1A P35348 1/20 0.46
HTR2B P41595 1/20 0.46
PDE4D Q08499 1/20 0.46
KCNH2 Q12809 1/20 0.46
TLR8 Q9NR97 2/20 0.42
FDPS P14324 1/20 0.35
PKM P14618 1/20 0.34
EGLN3 Q9H6Z9 1/20 0.34

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
Propionic Acid SCHEMBL7553163 0.93 TLR7 (0.65) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL29508382 0.85 TLR7 (1.00) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL189202 0.85 TLR7 (1.00) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL10732746 0.82 TLR7 (0.51) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL6719054 0.81 TLR7 (0.50) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL9602030 0.80 TLR7 (0.47) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL9601993 0.80 CYP11B1 (0.50) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL9385147 0.80 TLR7 (0.47) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL1774913 0.79 TLR7 (0.72) TLR7NUDT1LMNAPOLBHRH2
SCHEMBL29378640 0.79 TLR7 (0.72) TLR7NUDT1LMNAPOLBHRH2

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7939526-B2 Sulfone substituted imidazo ring ethers 3M INNOVATIVE PROPERTIES COMPANY (US) 2011-05-10 US disclosed
US-20070155767-A1 Sulfone substituted imidazo ring ethers 3M INNOVATIVE PROPERTIES COMPANY 2007-07-05 US disclosed
CN-1914203-A Sulfone substituted imidazo ring ethers 3M INNOVATIVE PROPERTIES CO (US) 2007-02-14 CN disclosed
EP-1694674-A2 SULFONE SUBSTITUTED IMIDAZO RING ETHERS 3M Innovative Properties Company (US) 2006-08-30 EP disclosed
US-7026482-B2 Process for preparing imidazoquinolinamines MEDICIS PHARMACEUTICAL CORPORATION 2006-04-11 US disclosed
WO-2005076783-A2 SULFONE SUBSTITUTED IMIDAZO RING ETHERS 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-08-25 WO disclosed
US-6897314-B2 Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY (US) 2005-05-24 US disclosed
US-20050096470-A1 Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY 2005-05-05 US disclosed
EP-0912565-B1 PROCESS FOR PREPARING IMIDAZOQUINOLINAMINES MINNESOTA MINING & MFG (US) 2004-04-14 EP disclosed
US-6624305-B2 Reacting a 6H-imidazo(4,5-c) tetrazolo(1,5-a)quinoline with triphenylphosphine and hydrolyzing 3M INNOVATIVE PROPERTIES COMPANY 2003-09-23 US disclosed
US-5998619-A Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY (US) 1999-12-07 US disclosed
US-5741908-A Process for reparing imidazoquinolinamines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-04-21 US disclosed
US-5693811-A Process for preparing tetrahdroimidazoquinolinamines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-12-02 US disclosed
US-5602256-A Process for 1H-imidazo[4,5-C]quinolines RIKER LABORATORIES, INC. (US) 1997-02-11 US disclosed
US-5578727-A Process for 1H-imidazo[4,5-c]quinolines RIKER LABORATORIES, INC. (US) 1996-11-26 US disclosed
EP-0425306-B1 Process for 1H-imidazo[4,5-c]-quinolines RIKER LABORATORIES INC (US) 1995-08-23 EP disclosed
EP-0425306-A2 Process for 1H-imidazo[4,5-c]-quinolines RIKER LABORATORIES, INC. (US) 1991-05-02 EP disclosed
US-4988815-A 3-Amino or 3-nitro quinoline compounds which are intermediates in preparing 1H-imidazo[4,5-c]quinolines RIKER LABORATORIES, INC. (US) 1991-01-29 US disclosed
US-4698348-A 1H-imidazo[4,5-c]quinolines and their use as bronchodilating agents RIKER LABORATORIES, INC. (US) 1987-10-06 US disclosed
US-4689338-A 1H-Imidazo[4,5-c]quinolin-4-amines and antiviral use RIKER LABORATORIES, INC. (US) 1987-08-25 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-20070155767-A1 Sulfone substituted imidazo ring ethers IL2, IL4, IFNG TLR7 82/4885NUDT1 2054/4885LMNA 4796/4885
US-20050096470-A1 Process for preparing imidazoquinolinamines ITPA, INMT, PIP4K2C TLR7 2042/4885NUDT1 15/4885LMNA 1093/4885

“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.