SCHEMBL4407292

SCHEMBL4407292

Cc1c(CCC(=O)Nc2ccccc2)c(C)n(C)c1C=O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 3/20 0.48
▸ HTT P42858 1/20 0.48
▸ PKM P14618 1/20 0.43
▸ PANK1 Q8TE04 1/20 0.43
▸ PANK3 Q9H999 1/20 0.43
▸ PTGDR2 Q9Y5Y4 1/20 0.43
▸ KDM4E B2RXH2 2/20 0.42
▸ HSP90B1 P14625 1/20 0.42
▸ ALDH1A1 P00352 3/20 0.42
▸ KMT2A Q03164 2/20 0.42
▸ POLB P06746 1/20 0.42
▸ LMNA P02545 1/20 0.42
▸ MEN1 O00255 1/20 0.42
▸ MAPK1 P28482 1/20 0.42
▸ EGFR P00533 1/20 0.42
▸ SRC P12931 1/20 0.42
▸ GAA P10253 1/20 0.42
▸ HPGD P15428 1/20 0.42
▸ SMN1; SMN2 Q16637 1/20 0.42
▸ RGS12 O14924 1/20 0.42

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
SCHEMBL4405756 0.88 MAPT (0.52) MAPTKDM4EALDH1A1KMT2APOLB
SCHEMBL4409427 0.86 L3MBTL1 (0.51) MAPTHTTPANK1PANK3ALDH1A1
SCHEMBL8219367 0.82 HTT (0.53) MAPTHTTPKMKDM4EALDH1A1
SCHEMBL4415982 0.78 NPSR1 (0.38) PKMKDM4EALDH1A1EGFRGAA
SCHEMBL17755717 0.69 MAPT (0.53) MAPTHTTPKMKDM4EALDH1A1
SCHEMBL17755721 0.68 MAPT (0.51) MAPTHTTPKMKDM4EALDH1A1
SCHEMBL29160657 0.68 NPC1 (0.53) MAPTKDM4EALDH1A1KMT2APOLB
SCHEMBL3342586 0.67 L3MBTL1 (0.80) MAPTHTTKDM4EALDH1A1EGFR
Methyl Alcohol SCHEMBL4593446 0.67 MAPT (0.93) MAPTHTTALDH1A1KMT2ALMNA
SCHEMBL4414249 0.67 LMNA (0.52) PTGDR2ALDH1A1KMT2ALMNAMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2020408-A1 Pyrrole substituted 2-indolinone protein kinase inhibitors Sugen, Inc. (US) 2009-02-04 — — EP disclosed
US-7189721-B2 Bicyclic protein kinase inhibitors SUGEN INC. (US) 2007-03-13 — — US disclosed
US-7119090-B2 Pyrrole substituted 2-indolinone protein kinase inhibitors SUGEN, INC. (US) 2006-10-10 — — US disclosed
US-6878733-B1 Formulations for pharmaceutical agents ionizable as free acids or free bases SUGEN, INC. (US) 2005-04-12 — — US disclosed
US-6855730-B2 3-methylidenyl-2-indolinone modulators of protein kinase SUGEN, INC. (US) 2005-02-15 — — US disclosed
US-20040106618-A1 Bicyclic protein kinase inhibitors SUGEN, INC. 2004-06-03 — — US disclosed
US-6696448-B2 USEFUL IN THE PREVENTION AND TREATMENT OF PROTEIN TYROSINE KINASE RELATED CELLULAR DISORDERS SUCH AS CANCER, DIABETES, AUTOIMMUNE DISORDERS, HYPERPROLIFERATIVE DISORDERS SUCH AS RHEUMATOID ARTHRITIS AND INFLAMMATORY DISORDERS SUGEN, INC. 2004-02-24 — — US disclosed
US-20040024010-A1 3-methylidenyl-2-indolinone modulators of protein kinase SUGEN, INC. 2004-02-05 — — US disclosed
US-6683082-B2 3-HETERO-ARYLIDENE-2-INDOLINONE COMPOUNDS; ANTICANCER AGENTS SUGEN, INC. 2004-01-27 — — US disclosed
US-6579897-B2 For therapy of cancer, arthritis, diabetic retinopathy, restinosis, hepatic cirrhosis, atherosclerosis, angiogenesis, glomerulonephritis, diabetic nephropathy, thrombic microangiopathy syndromes, transplant rejection SUGEN, INC. 2003-06-17 — — US disclosed
US-20020058661-A1 Bioavailability 3-heteroarylidenyl-2-indolinones active as protein tyrosine kinase inhibitors TANG PENG CHO (US) 2002-05-16 — — US disclosed
US-6350754-B2 ANTICARCINOGENIC AGENTS SUGEN, INC. 2002-02-26 — — US disclosed
US-20010056094-A1 Anticarcinogenic agents TANG PENG CHO (US) 2001-12-27 — — US disclosed
US-6316429-B1 ENZYME INHIBITORS MODULATE THE ACTIVITY OF PROTEIN KINASES AND THEREFORE ARE EXPECTED TO BE USEFUL IN THE PREVENTION AND TREATMENT OF PROTEIN KINASE RELATED CELLULAR DISORDERS SUCH AS CANCER. SUGEN, INC. 2001-11-13 — — US disclosed
US-6313158-B1 THERAPY AND PROPHYLAXIS OF CANCER SUGEN, INC. 2001-11-06 — — US disclosed
EP-1082305-A4 PYRROLE SUBSTITUTED 2-INDOLINONE PROTEIN KINASE INHIBITORS SUGEN INC (US) 2001-09-26 — — EP disclosed
WO-2001037820-A2 IONIZABLE INDOLINONE DERIVATIVES AND THEIR USE AS PTK LIGANDS SUGEN, INC. (US) 2001-05-31 — — WO disclosed
EP-1082305-A1 PYRROLE SUBSTITUTED 2-INDOLINONE PROTEIN KINASE INHIBITORS Sugen, Inc. (US) 2001-03-14 — — EP disclosed
US-6051593-A USEFUL IN THE PREVENTION AND TREATMENT OF PROTEIN TYROSINE KINASE RELATED CELLULAR DISORDERS SUCH AS CANCER SUGEN, INC. (US) 2000-04-18 — — US disclosed
WO-1999061422-A1 PYRROLE SUBSTITUTED 2-INDOLINONE PROTEIN KINASE INHIBITORS SUGEN, INC. (US) 1999-12-02 — — 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 (4 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-20010056094-A1 Anticarcinogenic agents GSTK1, CDC42BPG, GLS MAPT 4728/4885HTT 3559/4885PKM 1867/4885
US-20040106618-A1 Bicyclic protein kinase inhibitors MAP3K20, MAP4K3, MAP4K2 MAPT 3296/4885HTT 3823/4885PKM 489/4885
US-20040024010-A1 3-methylidenyl-2-indolinone modulators of protein kinase DMPK, MAP4K3, MAP3K20 MAPT 4113/4885HTT 4537/4885PKM 477/4885
US-20020058661-A1 Bioavailability 3-heteroarylidenyl-2-indolinones active as protein tyrosine kinase inhibitors TH, DSTYK, ERBB2 MAPT 3037/4885HTT 1514/4885PKM 1144/4885

“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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