SCHEMBL2914054

SCHEMBL2914054

Oc1ccc2sc(-c3ccccc3)nc2c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
APP P05067 5/20 0.66
RAB9A P51151 7/20 0.65
KDM4E B2RXH2 6/20 0.65
NPC1 O15118 6/20 0.65
MAPT P10636 5/20 0.65
LMNA P02545 3/20 0.65
ALDH1A1 P00352 3/20 0.65
GAA P10253 3/20 0.65
GLA P06280 2/20 0.65
NFKB1 P19838 6/20 0.64
NFKB2 Q00653 6/20 0.64
RELA Q04206 6/20 0.64
SMN1; SMN2 Q16637 6/20 0.64
POLB P06746 2/20 0.64
TP53 P04637 2/20 0.64
HSD17B10 Q99714 1/20 0.64
NPSR1 Q6W5P4 1/20 0.59
HPGD P15428 3/20 0.58
STAT1 P42224 1/20 0.58
PKM P14618 3/20 0.55

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
SCHEMBL3237813 0.86 APP (0.71) APPRAB9AKDM4ENPC1MAPT
SCHEMBL13391563 0.83 APP (0.77) APPRAB9AKDM4ENPC1MAPT
SCHEMBL2923164 0.83 APP (0.71) APPRAB9AKDM4ENPC1MAPT
SCHEMBL13806234 0.83 APP (0.77) APPRAB9AKDM4ENPC1MAPT
SCHEMBL3187010 0.81 KDM4E (0.68) APPRAB9AKDM4ENPC1MAPT
SCHEMBL27494065 0.81 RAB9A (0.96) APPRAB9AKDM4ENPC1MAPT
SCHEMBL1744060 0.80 SMN1; SMN2 (0.77) RAB9AKDM4ENPC1MAPTLMNA
SCHEMBL697049 0.80 KDM4E (0.71) APPRAB9AKDM4ENPC1MAPT
SCHEMBL27541328 0.80 KDM4E (0.55) APPRAB9AKDM4ENPC1MAPT
SCHEMBL17404415 0.80 KDM4E (0.66) APPRAB9AKDM4ENPC1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109180590-A A method of Benzoheterocyclic compounds are quickly prepared using physical grinding method under room temperature solvent-free 福建医科大学 2019-01-11 CN disclosed
EP-2222160-B1 HALOALLYLAMINE INHIBITORS OF SSAO/VAP-1 AND USES THEREFOR PHARMAXIS LTD (AU) 2015-03-18 EP disclosed
US-8426587-B2 Haloallylamine inhibitors of SSAO/VAP-1 and uses therefor PHARMAXIS LTD. (AU) 2013-04-23 US disclosed
US-20100298330-A1 HALOALLYLAMINE INHIBITORS OF SSAO/VAP-1 AND USES THEREFOR PHARMAXIS LTD. (AU) 2010-11-25 US disclosed
EP-2222160-A2 HALOALLYLAMINE INHIBITORS OF SSAO/VAP-1 AND USES THEREFOR Pharmaxis Ltd. (AU) 2010-09-01 EP disclosed
WO-2009066152-A2 HALOALLYLAMINE INHIBITORS OF SSAO/VAP-1 AND USES THEREFOR PHARMAXIS LTD. (US) 2009-05-28 WO disclosed
EP-1339701-B1 HETEROARYL ALKYL PIPERAZINE DERIVATIVES AS FATTY ACID OXIDATION INHIBITORS CV THERAPEUTICS INC (US) 2007-02-14 EP disclosed
US-6849632-B2 Heteroaryl alkyl piperazine derivatives CV THERAPEUTICS, INC. (US) 2005-02-01 US disclosed
US-20040192702-A1 Heteroaryl alkyl piperazine derivatives ZABLOCKI JEFF (US) 2004-09-30 US disclosed
US-20040029889-A1 Heteroaryl alkyl piperazine derivatives as fatty acid oxidation inhibitors CV THERAPEUTICS, INC. 2004-02-12 US disclosed
US-20030216409-A1 Heteroaryl alkyl piperazine derivatives CV THERAPEUTICS, INC. 2003-11-20 US disclosed
EP-1339701-A1 HETEROARYL ALKYL PIPERAZINE DERIVATIVES AS FATTY ACID OXIDATION INHIBITORS CV THERAPEUTICS, INC. (US) 2003-09-03 EP disclosed
US-6573264-B1 Protecting skeletal muscles against damage, treating shock conditions, preserving donor tissue and organs used in transplants, treating cardiovascular diseases CV THERAPEUTICS, INC. 2003-06-03 US disclosed
WO-2002064576-A1 HETEROARYL ALKYL PIPERAZINE DERIVATIVES AS FATTY ACID OXIDATION INHIBITORS CV THERAPEUTICS, INC. (US) 2002-08-22 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-20040029889-A1 Heteroaryl alkyl piperazine derivatives as fatty acid oxidation inhibitors CPT1B, CPT1A, ALOX15 APP 4118/4885RAB9A 2974/4885KDM4E 4148/4885
US-20040192702-A1 Heteroaryl alkyl piperazine derivatives ATP2A1, CPT1B, ATP2A3 APP 4270/4885RAB9A 2107/4885KDM4E 4298/4885
US-20100298330-A1 HALOALLYLAMINE INHIBITORS OF SSAO/VAP-1 AND USES THEREFOR VAPA, SLC6A11, VAPB APP 1634/4885RAB9A 3543/4885KDM4E 3842/4885
US-20030216409-A1 Heteroaryl alkyl piperazine derivatives ATP2A1, CPT1B, ATP2A3 APP 4270/4885RAB9A 2107/4885KDM4E 4298/4885

“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.