SCHEMBL6477287

SCHEMBL6477287

NNC(=O)c1sc2ccccc2c1Cl

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OGG1 O15527 2/20 1.00
HDAC1 Q13547 1/20 0.73
HDAC8 Q9BY41 1/20 0.73
HDAC6 Q9UBN7 1/20 0.73
MCL1 Q07820 1/20 0.65
RAB9A P51151 8/20 0.64
NPC1 O15118 7/20 0.64
MAPT P10636 11/20 0.61
SMN1; SMN2 Q16637 7/20 0.61
ALDH1A1 P00352 6/20 0.61
KDM4E B2RXH2 4/20 0.61
GAA P10253 3/20 0.61
TP53 P04637 3/20 0.61
LMNA P02545 3/20 0.61
RXFP1 Q9HBX9 1/20 0.61
KMT2A Q03164 4/20 0.59
MEN1 O00255 3/20 0.59
HPGD P15428 2/20 0.59
PRNP P04156 1/20 0.59
PKM P14618 1/20 0.59

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
SCHEMBL1886020 0.85 HDAC1 (1.00) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL7984062 0.83 HDAC1 (0.79) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL10148327 0.83 OGG1 (0.71) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL8631382 0.83 OGG1 (0.70) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL29285354 0.81 OGG1 (0.69) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL7675240 0.81 MCL1 (0.71) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL5935569 0.81 MAPT (0.79) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL7088656 0.80 MCL1 (0.76) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL25774012 0.80 OGG1 (0.67) OGG1HDAC1HDAC8HDAC6MCL1
SCHEMBL12768191 0.80 HDAC1 (0.68) OGG1HDAC1HDAC8HDAC6MCL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11535597-B2 Photoreactive ligands and uses thereof THE SCRIPPS RESEARCH INSTITUTE (US) 2022-12-27 US disclosed
US-20200071277-A1 PHOTOREACTIVE LIGANDS AND USES THEREOF THE SCRIPPS RESEARCH INSTITUTE 2020-03-05 US disclosed
US-20170038365-A1 SMALL MOLECULE INHIBITORS OF 8-OXOGUANINE DNA GLYCOSYLASE-1 (OGG1) OREGON HEALTH & SCIENCE UNIVERSITY (US) 2017-02-09 US disclosed
US-20170038365-A1 SMALL MOLECULE INHIBITORS OF 8-OXOGUANINE DNA GLYCOSYLASE-1 (OGG1) OREGON HEALTH & SCIENCE UNIVERSITY (US) 2017-02-09 US disclosed
US-6887863-B2 Hydrazide and alkoxyamide angiogenesis inhibitors ABBOTT LABORATORIES (US) 2005-05-03 US disclosed
EP-1272456-B1 HYDRAZIDE AND ALKOXYAMIDE ANGIOGENESIS INHIBITORS ABBOTT LAB (US) 2004-10-27 EP disclosed
US-20040167126-A1 Hydrazide and alkoxyamide angiogenesis inhibitors ABBVIE INC. 2004-08-26 US disclosed
US-6747052-B2 ANTICANCER AGENTS CYTOVIA, INC. 2004-06-08 US disclosed
US-20030105140-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2003-06-05 US disclosed
EP-1272456-A1 HYDRAZIDE AND ALKOXYAMIDE ANGIOGENESIS INHIBITORS Abbott Laboratories (US) 2003-01-08 EP disclosed
WO-2002102301-A2 SUBSTITUTED INDOLE-2-CARBOXYLIC ACID BENZYLIDENE-HYDRAZIDES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF CYTOVIA, INC. (US) 2002-12-27 WO disclosed
US-20020128292-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof CYTOVIA, INC. 2002-09-12 US disclosed
US-20020002152-A1 Hydrazide and alkoxyamide angiogenesis inhibitors ABBOTT LABORATORIES 2002-01-03 US disclosed
WO-2001079157-A1 HYDRAZIDE AND ALKOXYAMIDE ANGIOGENESIS INHIBITORS ABBOTT LABORATORIES (US) 2001-10-25 WO disclosed
US-5863936-A HETEROCYCLIC ENZYME INHIBITORS AS ANTICANCER AGENTS GERON CORPORATION (US) 1999-01-26 US disclosed
US-5760062-A ANTICANCER AGENTS GERON CORPORATION (US) 1998-06-02 US disclosed
US-5703116-A TREATING CANCER GERON CORPORATION (US) 1997-12-30 US disclosed
US-4269846-A BENZOHETEROCYCLIC OXADIAZOLONES AND TRIAZOLONES USV PHARMACEUTICAL CORPORATION (US) 1981-05-26 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 (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-11535597-B2 Photoreactive ligands and uses thereof CLTB, CRYAB, CRYAA OGG1 3281/4885HDAC1 4007/4885HDAC8 3494/4885
US-20020128292-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof BAD, API5, CASP2 OGG1 2317/4885HDAC1 87/4885HDAC8 290/4885
US-20030105140-A1 Substituted indole-2-carboxylic acid benzylidene-hydrazides and analogs as activators of caspases and inducers of apoptosis and the use thereof BAD, API5, CASP2 OGG1 2317/4885HDAC1 87/4885HDAC8 290/4885
US-20040167126-A1 Hydrazide and alkoxyamide angiogenesis inhibitors METAP2, METAP1, ANPEP OGG1 3275/4885HDAC1 356/4885HDAC8 1824/4885
US-20200071277-A1 PHOTOREACTIVE LIGANDS AND USES THEREOF CLTB, CRYAB, CRYAA OGG1 3281/4885HDAC1 4007/4885HDAC8 3494/4885
US-20020002152-A1 Hydrazide and alkoxyamide angiogenesis inhibitors METAP2, METAP1, ANPEP OGG1 3275/4885HDAC1 356/4885HDAC8 1824/4885

“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.