SCHEMBL5377919

SCHEMBL5377919

CC(=O)n1nc(-c2ccccc2)c2cc(N)ccc21

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PTGER1 P34995 1/20 0.47
▸ CSNK1A1 P48729 2/20 0.47
▸ GSK3A P49840 2/20 0.47
▸ CLK4 Q9HAZ1 2/20 0.47
▸ DYRK1B Q9Y463 2/20 0.47
▸ CHEK1 O14757 1/20 0.47
▸ AURKA O14965 1/20 0.47
▸ DAPK3 O43293 1/20 0.47
▸ LIMK1 P53667 1/20 0.47
▸ IKBKE Q14164 1/20 0.47
▸ MAPK14 Q16539 1/20 0.47
▸ TAOK1 Q7L7X3 1/20 0.47
▸ KDM4E B2RXH2 3/20 0.43
▸ RORC P51449 2/20 0.43
▸ MAPT P10636 1/20 0.42
▸ CDK5 Q00535 2/20 0.42
▸ PDGFRA P16234 1/20 0.42
▸ TYRO3 Q06418 1/20 0.42
▸ NR1H2 P55055 1/20 0.41
▸ NR1H3 Q13133 1/20 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
SCHEMBL5377771 0.83 PRMT1 (0.46) KDM4EMAPTKMT2AELANEALDH1A1
SCHEMBL4006762 0.82 MAP2K4 (0.58) PTGER1KDM4ERORCMAPTNR1H2
SCHEMBL5372323 0.80 LMNA (0.53) KDM4EMAPTKMT2AELANEALDH1A1
SCHEMBL4327851 0.76 PTGER1 (0.45) PTGER1KDM4EELANEMAP2K4
SCHEMBL7148004 0.75 RORC (0.43) KDM4ERORCNR1H2NR1H3KMT2A
SCHEMBL5381037 0.74 LMNA (0.50) KDM4EKMT2AKDRALDH1A1LMNA
SCHEMBL27618323 0.74 KDM4E (0.49) PTGER1CSNK1A1CLK4CHEK1AURKA
SCHEMBL2571241 0.73 CHEK1 (0.48) CSNK1A1GSK3ACLK4DYRK1BCHEK1
SCHEMBL5383368 0.72 PTPN1 (0.52) KDM4EMAPTKMT2AELANEALDH1A1
SCHEMBL5381752 0.72 RORC (0.49) PTGER1RORCHPGDRARGMAP2K4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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-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-20070060616-A1 Methods for treating, preventing and managing chronic lymphocytic leukemia with indazole compounds SIGNAL PHARMACEUTICALS, LLC 2007-03-15 — — US disclosed
EP-1618093-A2 INDAZOLE DERIVATIVES AS JNK INHIBITORS Signal Pharmaceuticals LLC (US) 2006-01-25 — — EP disclosed
US-6897231-B2 Indazole derivatives as JNK inhibitors and compositions and methods related thereto SIGNAL PHARMACEUTICALS, INC. (US) 2005-05-24 — — US disclosed
US-20050107457-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto SINGNAL PHARMACEUTICALS, INC. 2005-05-19 — — US disclosed
US-20050009876-A1 Indazole compounds, compositions thereof and methods of treatment therewith SIGNAL PHARMACEUTICALS, LLC 2005-01-13 — — US disclosed
WO-2004094388-A2 INDAZOLE DERIVATIVES AS JNK INHIBITORS SIGNAL PHARMACEUTICALS, LLC (US) 2004-11-04 — — WO disclosed
US-20040127536-A1 Methods for treating an inflammatory condition or inhibiting JNK SIGNAL PHARMACEUTICALS, LLC 2004-07-01 — — 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
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

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 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-20040127536-A1 Methods for treating an inflammatory condition or inhibiting JNK MAPK1, MAP3K1, MAPKAPK2 PTGER1 798/4885CSNK1A1 117/4885GSK3A 362/4885
US-20040077877-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto MAP3K7, MAP3K1, MAP3K8 PTGER1 1018/4885CSNK1A1 72/4885GSK3A 214/4885
US-20070060616-A1 Methods for treating, preventing and managing chronic lymphocytic leukemia with indazole compounds BCL9, MCL1, INMT PTGER1 3407/4885CSNK1A1 1057/4885GSK3A 1098/4885
US-20050107457-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto MAP3K7, MAP3K1, MAP3K8 PTGER1 988/4885CSNK1A1 86/4885GSK3A 269/4885
US-20020103229-A1 Indazole derivatives as JNK inhibitors and compositions and methods related thereto MAP3K7, MAP3K1, MAP3K8 PTGER1 1018/4885CSNK1A1 72/4885GSK3A 214/4885
US-20050009876-A1 Indazole compounds, compositions thereof and methods of treatment therewith GPR119, JAK3, IGF1R PTGER1 1357/4885CSNK1A1 181/4885GSK3A 22/4885

“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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