SCHEMBL741856

SCHEMBL741856

COc1ccc2c(=O)[nH]c(C)cc2c1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ AXL P30530 1/20 0.59
▸ KDM4E B2RXH2 6/20 0.56
▸ GAA P10253 2/20 0.56
▸ HSD17B10 Q99714 2/20 0.54
▸ LMNA P02545 1/20 0.54
▸ ALDH1A1 P00352 4/20 0.53
▸ HPGD P15428 1/20 0.53
▸ PARP15 Q460N3 1/20 0.48
▸ PARP14 Q460N5 1/20 0.48
▸ PARP10 Q53GL7 1/20 0.48
▸ TNKS2 Q9H2K2 1/20 0.48
▸ PARP2 Q9UGN5 1/20 0.48
▸ TUBB4A P04350 2/20 0.47
▸ TUBB P07437 2/20 0.47
▸ TUBA3C P0DPH7 2/20 0.47
▸ TUBA1B P68363 2/20 0.47
▸ TUBA4A P68366 2/20 0.47
▸ TUBB4B P68371 2/20 0.47
▸ TUBB3 Q13509 2/20 0.47
▸ TUBB2A Q13885 2/20 0.47

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
SCHEMBL7715523 0.86 KDM4E (0.58) AXLKDM4EGAAHSD17B10LMNA
SCHEMBL28582802 0.82 KDM4E (0.47) AXLKDM4EGAAHSD17B10LMNA
SCHEMBL26018335 0.81 KDM4E (0.49) AXLKDM4EGAAHSD17B10LMNA
SCHEMBL4773470 0.79 PARP1 (0.58) KDM4EGAALMNAALDH1A1HPGD
SCHEMBL824579 0.78 KDM4E (0.63) KDM4EGAALMNAALDH1A1TUBB4A
SCHEMBL1536353 0.76 KDM4E (0.64) KDM4EHSD17B10LMNAALDH1A1HPGD
SCHEMBL16740907 0.76 LMNA (0.64) AXLKDM4EGAAHSD17B10LMNA
SCHEMBL26785799 0.76 PARP15 (0.58) KDM4EGAAHSD17B10LMNAALDH1A1
SCHEMBL29853659 0.76 PARP15 (0.58) KDM4EGAAHSD17B10LMNAALDH1A1
SCHEMBL392734 0.75 GAA (0.59) KDM4EGAALMNAHPGDTNKS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112876419-A Allylamine derivatives, process for producing the same and use thereof 四川科伦博泰生物医药股份有限公司 2021-06-01 — — CN disclosed
US-8518874-B2 HCV inhibitors VIROBAY, INC. (US) 2013-08-27 — — US disclosed
US-8518874-B2 HCV inhibitors VIROBAY, INC. (US) 2013-08-27 — — US disclosed
US-8518874-B2 HCV inhibitors VIROBAY, INC. (US) 2013-08-27 — — US disclosed
US-8211897-B2 Inhibitors of cathepsin B VIROBAY, INC. (US) 2012-07-03 — — US disclosed
US-8211897-B2 Inhibitors of cathepsin B VIROBAY, INC. (US) 2012-07-03 — — US disclosed
US-8211897-B2 Inhibitors of cathepsin B VIROBAY, INC. (US) 2012-07-03 — — US disclosed
EP-2431379-A2 HCV inhibitors Virobay, Inc. (US) 2012-03-21 — — EP disclosed
EP-2431379-A2 HCV inhibitors Virobay, Inc. (US) 2012-03-21 — — EP disclosed
EP-2340830-A2 Hepatitis C Virus Inhibitors Bristol-Myers Squibb Company (US) 2011-07-06 — — EP disclosed
WO-2009100225-A1 INHIBITORS OF CATHEPSIN B VIROBAY, INC. (US) 2009-08-13 — — WO disclosed
WO-2009100225-A1 INHIBITORS OF CATHEPSIN B VIROBAY, INC. (US) 2009-08-13 — — WO disclosed
EP-1745024-A4 1-ARYL-4-SUBSTITUTED ISOQUINOLINES NEUROGEN CORP (US) 2008-01-09 — — EP disclosed
US-20070249665-A1 1-aryl-4-substituted isoquinolines NEUROGEN CORPORATION (US) 2007-10-25 — — US disclosed
US-20070054864-A1 1-[2S-(3-Tert-butylureido)-3,3-dimethylbutyryl]-4R-(7-methoxy-2-pyrazol-1-yl-quinolin-4-yloxy)-pyrrolidine-2S-carboxylic acid (1S-cyclopropylaminooxalylbutyl)amide, for example; useful in treating hepatitis C infections QUEST DIAGNOSTICS INVESTMENTS LLC 2007-03-08 — — US disclosed
US-20070054864-A1 1-[2S-(3-Tert-butylureido)-3,3-dimethylbutyryl]-4R-(7-methoxy-2-pyrazol-1-yl-quinolin-4-yloxy)-pyrrolidine-2S-carboxylic acid (1S-cyclopropylaminooxalylbutyl)amide, for example; useful in treating hepatitis C infections QUEST DIAGNOSTICS INVESTMENTS LLC 2007-03-08 — — US disclosed
US-20070054864-A1 1-[2S-(3-Tert-butylureido)-3,3-dimethylbutyryl]-4R-(7-methoxy-2-pyrazol-1-yl-quinolin-4-yloxy)-pyrrolidine-2S-carboxylic acid (1S-cyclopropylaminooxalylbutyl)amide, for example; useful in treating hepatitis C infections QUEST DIAGNOSTICS INVESTMENTS LLC 2007-03-08 — — US disclosed
EP-1745024-A1 1-ARYL-4-SUBSTITUTED ISOQUINOLINES NEUROGEN CORPORATION (US) 2007-01-24 — — EP disclosed
WO-2007005838-A2 HCV INHIBITORS VIROBAY, INC. (US) 2007-01-11 — — WO disclosed
WO-2005110991-A1 1-ARYL-4-SUBSTITUTED ISOQUINOLINES NEUROGEN CORPORATION (US) 2005-11-24 — — 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 (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-20070249665-A1 1-aryl-4-substituted isoquinolines C3AR1, C5AR1, C5AR2 AXL 743/4885KDM4E 2418/4885GAA 4844/4885
US-20070054864-A1 1-[2S-(3-Tert-butylureido)-3,3-dimethylbutyryl]-4R-(7-methoxy-2-pyrazol-1-yl-quinolin-4-yloxy)-pyrrolidine-2S-carboxylic acid (1S-cyclopropylaminooxalylbutyl)amide, for example; useful in treating hepatitis C infections HAVCR2, EIF2AK2, GTF3C1 AXL 3757/4885KDM4E 536/4885GAA 716/4885

“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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