SCHEMBL4093740

SCHEMBL4093740

Cc1ccc2[nH]nc(-c3ccccc3)c2c1

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAP2K4 P45985 10/20 0.71
MAPK1 P28482 5/20 0.71
MAPKAPK3 Q16644 5/20 0.71
MAPK6 Q16659 5/20 0.71
MAPKAPK2 P49137 4/20 0.71
MAPKAPK5 Q8IW41 3/20 0.71
DCLK1 O15075 1/20 0.65
PRKD3 O94806 1/20 0.65
MAP4K4 O95819 1/20 0.65
CHEK2 O96017 1/20 0.65
CSF1R P07333 1/20 0.65
FER P16591 1/20 0.65
CDK2 P24941 1/20 0.65
MARK3 P27448 1/20 0.65
FLT4 P35916 1/20 0.65
FLT3 P36888 1/20 0.65
MAPK9 P45984 1/20 0.65
CSNK1D P48730 1/20 0.65
CLK2 P49760 1/20 0.65
CSNK2A1 P68400 1/20 0.65

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
SCHEMBL4005413 0.86 MAP2K4 (0.65) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL22819364 0.83 MAP2K4 (1.00) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL22801614 0.83 MAP2K4 (1.00) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL5374591 0.83 MAP2K4 (0.71) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL17306449 0.81 MKNK1 (0.87) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL22819363 0.81 MAP2K4 (1.00) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL8251865 0.80 MAP2K4 (0.68) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL22819367 0.79 MAP2K4 (1.00) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL5509470 0.79 MKNK1 (0.61) MAP2K4MAPK1MAPKAPK3MAPK6MAPKAPK2
SCHEMBL16862707 0.79 MAPK10 (0.67) MAP2K4DCLK1PRKD3MAP4K4CHEK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20220170904-A1 SYSTEMS AND METHODS FOR MONITORING BIOLOGICAL TISSUE DEGRADATION ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2022-06-02 US disclosed
EP-2065383-A1 Indazole compounds and methods of use thereof as protein kinase inhibitors Signal Pharmaceuticals, Inc. (US) 2009-06-03 EP disclosed
US-20090099178-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF BHAGWAT SHRIPAD S 2009-04-16 US disclosed
US-7220771-B2 Methods of using indazole derivatives as JNK inhibitors SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-22 US disclosed
US-7220771-B2 Methods of using indazole derivatives as JNK inhibitors SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-22 US disclosed
US-7220771-B2 Methods of using indazole derivatives as JNK inhibitors SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-22 US disclosed
US-7211594-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-01 US disclosed
US-7211594-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-01 US disclosed
US-7211594-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-01 US disclosed
US-7208513-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-04-24 US disclosed
US-20040077877-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto SIGNAL PHARMACEUTICALS, INC. 2004-04-22 US disclosed
EP-1313711-A2 INDAZOLE DERIVATIVES AS JNK INHIBITORS SIGNAL PHARMACEUTICALS, INC. (US) 2003-05-28 EP disclosed
WO-2002010137-A9 INDAZOLE DERIVATIVES AS JNK INHIBITORS SIGNAL PHARM INC (US) 2003-02-06 WO disclosed
WO-2002010137-A9 INDAZOLE DERIVATIVES AS JNK INHIBITORS SIGNAL PHARM INC (US) 2003-02-06 WO disclosed
US-20020103229-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto SIGNAL PHARMACEUTICALS, LLC 2002-08-01 US disclosed
WO-2002010137-A2 INDAZOLE DERIVATIVES AS JNK INHIBITORS SIGNAL PHARMACEUTICALS, INC. (US) 2002-02-07 WO disclosed
US-4409234-A Pyrazoloindazole derivatives and bronchodilating composition CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 1983-10-11 US disclosed
EP-0023633-B1 PYRAZOLOINDAZOLE DERIVATIVES AND PROCESS FOR PREPARING THE SAME AND PHARMACEUTICAL COMPOSITIONS Chugai Seiyaku Kabushiki Kaisha (JP) 1982-11-24 EP disclosed
EP-0023633-A1 Pyrazoloindazole derivatives and process for preparing the same and pharmaceutical compositions Chugai Seiyaku Kabushiki Kaisha (JP) 1981-02-11 EP disclosed
US-3994890-A TRANQUILIZERS, ANTIDEPRESSANTS, ANTIINFLAMMATORY CHUGAI SEIYAKU KABUSHIKI KAISHA (JA) 1976-11-30 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-20040077877-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto MAP3K7, MAP3K1, MAP3K8 MAP2K4 71/4885MAPK1 16/4885MAPKAPK3 21/4885
US-20020103229-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto MAP3K7, MAP3K1, MAP3K8 MAP2K4 71/4885MAPK1 16/4885MAPKAPK3 21/4885
US-20090099178-A1 INDAZOLE COMPOUNDS AND METHODS OF USE THEREOF WNT3, WNT3A, WNK3 MAP2K4 358/4885MAPK1 171/4885MAPKAPK3 23/4885

“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.