SCHEMBL6099859

SCHEMBL6099859

CCOC(=O)c1ccccc1-n1nnnc1C

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 2/20 0.54
▸ OPRM1 P35372 1/20 0.48
▸ ALDH1A1 P00352 6/20 0.48
▸ HSD17B10 Q99714 3/20 0.48
▸ MAPK1 P28482 4/20 0.46
▸ MAPT P10636 3/20 0.46
▸ SMN1; SMN2 Q16637 2/20 0.46
▸ GAA P10253 1/20 0.46
▸ TP53 P04637 1/20 0.46
▸ ALOX12 P18054 1/20 0.46
▸ POLB P06746 1/20 0.45
▸ APEX1 P27695 1/20 0.45
▸ RECQL P46063 1/20 0.45
▸ CTDSP1 Q9GZU7 1/20 0.45
▸ TDP1 Q9NUW8 1/20 0.45
▸ L3MBTL1 Q9Y468 1/20 0.45
▸ HPGD P15428 2/20 0.45
▸ KMT2A Q03164 1/20 0.43
▸ SLC5A1 P13866 1/20 0.43
▸ SLC5A2 P31639 1/20 0.43

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
SCHEMBL3353271 0.83 RAB9A (0.41) TSHRALDH1A1MAPK1SMN1; SMN2TP53
SCHEMBL1486496 0.83 CA12 (0.54) TSHROPRM1MAPK1LMNA
SCHEMBL3353715 0.80 OPRK1 (0.47) TSHRALDH1A1HSD17B10TP53ALOX12
SCHEMBL1486817 0.79 MEN1 (0.54) MAPTL3MBTL1HPGDKMT2ALMNA
SCHEMBL1486749 0.79 KDM4E (0.40) TSHRALDH1A1HSD17B10MAPK1SMN1; SMN2
SCHEMBL4215375 0.74 MAPK1 (0.57) TSHRALDH1A1HSD17B10MAPK1MAPT
SCHEMBL2209512 0.73 TSHR (0.65) TSHRALDH1A1HSD17B10MAPK1MAPT
SCHEMBL17172445 0.73 MYC (0.71) TSHRALDH1A1HSD17B10MAPK1MAPT
SCHEMBL5971730 0.73 TSHR (0.51) TSHROPRM1ALDH1A1HSD17B10MAPK1
SCHEMBL12843980 0.73 ALOX15 (0.52) ALDH1A1SMN1; SMN2TP53ALOX12KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7026482-B2 Process for preparing imidazoquinolinamines MEDICIS PHARMACEUTICAL CORPORATION 2006-04-11 — — US 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
US-20040072858-A1 Heterocyclic ether substituted imidazoquinolines 3M INNOVATIVE PROPERTIES COMPANY 2004-04-15 — — US disclosed
EP-0912565-B1 PROCESS FOR PREPARING IMIDAZOQUINOLINAMINES MINNESOTA MINING & MFG (US) 2004-04-14 — — EP disclosed
US-20040019213-A1 Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY 2004-01-29 — — US disclosed
US-6664260-B2 Viricides; anticarcinogneic agents; induction cytokine biosynthesis 3M INNOVATIVE PROPERTIES COMPANY 2003-12-16 — — US 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
EP-1339715-A2 HETEROCYCLIC ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M Innovative Properties Company (US) 2003-09-03 — — EP disclosed
US-6613902-B2 Induce biosynthesis of cytokines such as interferons, interleukins, and tumor necrosis factor in humans and in mice. 3M INNOVATIVE PROPERTIES COMPANY 2003-09-02 — — US disclosed
US-6437131-B1 REACTING A 6H-IMIDAZO(4,5-C)TETRAZOLO(1,5-A)QUINOLINE WITH TRIPHENYLPHOSPHINE, HYDROLYZING TO FORM 1H-IMIDAZO(4,5-C) QUINOLIN-4-AMINES; INTERMEDIATE IS A 4-NITROTETRAZOLO(1,5-A) QUINOLIN-5-SULFONATE IN THE PR 3M INNOVATIVE PROPERTIES COMPANY 2002-08-20 — — US disclosed
WO-2002046193-A2 HETEROCYCLIC ETHER SUBSTITUTED IMIDAZOQUINOLINES 3M INNOVATIVE PROPERTIES COMPANY (US) 2002-06-13 — — WO disclosed
US-6150523-A Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY (US) 2000-11-21 — — US disclosed
US-5998619-A Process for preparing imidazoquinolinamines 3M INNOVATIVE PROPERTIES COMPANY (US) 1999-12-07 — — US disclosed
EP-0912565-A1 PROCESS FOR PREPARING IMIDAZOQUINOLINAMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1999-05-06 — — EP disclosed
EP-0912564-A1 PROCESS FOR PREPARING TETRAHYDROIMIDAZOQUINOLINAMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1999-05-06 — — EP disclosed
US-5741908-A Process for reparing imidazoquinolinamines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1998-04-21 — — US disclosed
WO-1997048703-A1 PROCESS FOR PREPARING TETRAHYDROIMIDAZOQUINOLINAMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-12-24 — — WO disclosed
WO-1997048704-A1 PROCESS FOR PREPARING IMIDAZOQUINOLINAMINES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-12-24 — — WO disclosed
US-5693811-A Process for preparing tetrahdroimidazoquinolinamines MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-12-02 — — 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 (3 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-20040019213-A1 Process for preparing imidazoquinolinamines VAT1, QARS1, TALDO1 TSHR 3957/4885OPRM1 2941/4885ALDH1A1 1648/4885
US-20050096470-A1 Process for preparing imidazoquinolinamines ITPA, INMT, PIP4K2C TSHR 3050/4885OPRM1 1943/4885ALDH1A1 1777/4885
US-20040072858-A1 Heterocyclic ether substituted imidazoquinolines IFNG, IL2, IRF3 TSHR 2857/4885OPRM1 2821/4885ALDH1A1 2486/4885

“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.

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