SCHEMBL945366

SCHEMBL945366

NC(=O)c1ccc(-c2ccccn2)nc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
P4HTM Q9NXG6 4/20 0.68
HPGDS O60760 2/20 0.56
CHEK2 O96017 2/20 0.54
NNMT P40261 3/20 0.52
SMN1; SMN2 Q16637 2/20 0.52
F7 P08709 1/20 0.52
F3 P13726 1/20 0.52
SARM1 Q6SZW1 1/20 0.52
SIRT2 Q8IXJ6 1/20 0.52
SIRT6 Q8N6T7 1/20 0.52
SIRT1 Q96EB6 1/20 0.52
SIRT3 Q9NTG7 1/20 0.52
SIRT5 Q9NXA8 1/20 0.52
SIRT4 Q9Y6E7 1/20 0.52
KDM4E B2RXH2 3/20 0.50
LMNA P02545 2/20 0.50
P4HA1 P13674 2/20 0.50
POLB P06746 2/20 0.50
BLM P54132 2/20 0.50
CYP1A2 P05177 1/20 0.50

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
Hydrochloric Acid SCHEMBL28173955 0.98 P4HTM (0.66) P4HTMHPGDSCHEK2NNMTSMN1; SMN2
SCHEMBL19581478 0.87 NNMT (0.65) P4HTMHPGDSNNMTSMN1; SMN2F7
Dipyridyl SCHEMBL15380517 0.85 TDP1 (0.67) P4HTMCHEK2SMN1; SMN2F7F3
SCHEMBL687378 0.84 P4HTM (0.74) P4HTMHPGDSSMN1; SMN2KDM4ELMNA
SCHEMBL3408513 0.84 HPGDS (0.55) P4HTMHPGDSCHEK2NNMTSMN1; SMN2
SCHEMBL29913684 0.84 P4HTM (0.74) P4HTMHPGDSSMN1; SMN2KDM4ELMNA
SCHEMBL28576114 0.84 P4HTM (0.70) P4HTMHPGDSSMN1; SMN2KDM4ELMNA
Hydrochloric Acid SCHEMBL29488111 0.82 P4HTM (0.71) P4HTMHPGDSSMN1; SMN2KDM4ELMNA
SCHEMBL29488117 0.82 P4HTM (0.71) P4HTMHPGDSSMN1; SMN2KDM4ELMNA
Dipyridyl SCHEMBL28724644 0.81 KDM4E (0.56) P4HTMCHEK2SMN1; SMN2F7F3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115531554-B Synthetic lethal nano-drug combination carrier and application thereof in preparation of GBM targeted drugs 河南大学 2023-08-11 CN claimed
US-20250263407-A1 Compounds STEP PHARMA S.A.S. (FR) 2025-08-21 US disclosed
US-11851428-B2 Activator of TREK (TWIK RElated K+channels) channels ONO PHARMACEUTICAL CO., LTD. (JP) 2023-12-26 US disclosed
US-20210347773-A1 ACTIVATOR OF TREK (TWIK RELATED K+ CHANNELS) CHANNELS ONO PHARMACEUTICAL CO., LTD. (JP) 2021-11-11 US disclosed
US-11046683-B2 Activator of TREK (TWIK RElated K+ channels) channels ONO PHARMACEUTICAL CO., LTD. (JP) 2021-06-29 US disclosed
US-20200339569-A1 1,2,4-OXADIAZOLE DERIVATIVES AS HISTONE DEACETYLASE 6 INHIBITORS ORYZON GENOMICS, S.A. (ES) 2020-10-29 US disclosed
CN-110402141-A The conjoint therapy of Axl inhibitor and EGFR tyrosine kinase inhibitor DAIICHI SANKYO CO LTD 2019-11-01 CN disclosed
US-20190322662-A1 ACTIVATOR OF TREK (TWIK RELATED K+ CHANNELS) CHANNELS ONO PHARMACEUTICAL CO., LTD. (JP) 2019-10-24 US disclosed
CN-105939998-B Heteroaryl compound and application thereof as BTK inhibitor 默克专利有限公司 2019-04-16 CN disclosed
CN-107209186-A The measure of BTK inhibitor 默克专利有限公司 2017-09-26 CN disclosed
US-20110009410-A1 APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS GILEAD SCIENCES, INC. (US) 2011-01-13 US disclosed
EP-1720542-A4 ARYLALKYLAMINO-SUBSTITUTED QUINAZOLINE ANALOGUES NEUROGEN CORP (US) 2007-11-28 EP disclosed
EP-1720542-A1 ARYLALKYLAMINO-SUBSTITUTED QUINAZOLINE ANALOGUES NEUROGEN CORPORATION (US) 2006-11-15 EP disclosed
EP-1581225-A1 COMBINATION THERAPY FOR THE TREATMENT OF PAIN NEUROGEN CORPORATION (US) 2005-10-05 EP disclosed
WO-2005087227-A1 ARYLALKYLAMINO-SUBSTITUTED QUINAZOLINE ANALOGUES NEUROGEN CORPORATION (US) 2005-09-22 WO disclosed
EP-1569926-A1 CARBOXYLIC ACID, PHOSPHATE OR PHOSPHONATE SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS NEUROGEN CORPORATION (US) 2005-09-07 EP disclosed
EP-1471910-A2 SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS MODULATORS OF CAPSAICIN RECEPTORS NEUROGEN CORPORATION (US) 2004-11-03 EP disclosed
WO-2004055004-A1 CARBOXYLIC ACID, PHOSPHATE OR PHOSPHONATE SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS CAPSAICIN RECEPTOR MODULATORS NEUROGEN CORPORATION (US) 2004-07-01 WO disclosed
WO-2004054582-A1 COMBINATION THERAPY FOR THE TREATMENT OF PAIN NEUROGEN CORPORATION (US) 2004-07-01 WO disclosed
WO-2003062209-A2 SUBSTITUTED QUINAZOLIN-4-YLAMINE ANALOGUES AS MODULATORS OF CAPSAICIN NEUROGEN CORPORATION (US) 2003-07-31 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 (7 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-20200339569-A1 1,2,4-OXADIAZOLE DERIVATIVES AS HISTONE DEACETYLASE 6 INHIBITORS HDAC6, HDAC1, HDAC3 P4HTM 2628/4885HPGDS 1668/4885CHEK2 1702/4885
US-20250263407-A1 Compounds CYP1A1, UGT1A1, CYP1A2 P4HTM 2315/4885HPGDS 1204/4885CHEK2 1278/4885
US-20110009410-A1 APOPTOSIS SIGNAL-REGULATING KINASE INHIBITORS BAX, CASP1, AIFM1 P4HTM 4408/4885HPGDS 1340/4885CHEK2 399/4885
US-11851428-B2 Activator of TREK (TWIK RElated K+channels) channels KCNJ11, KCNJ1, KCNJ8 P4HTM 2204/4885HPGDS 1223/4885CHEK2 1202/4885
US-20190322662-A1 ACTIVATOR OF TREK (TWIK RELATED K+ CHANNELS) CHANNELS KCNJ11, KCNJ1, KCNJ8 P4HTM 2204/4885HPGDS 1223/4885CHEK2 1202/4885
US-11046683-B2 Activator of TREK (TWIK RElated K+ channels) channels KCNJ11, KCNJ1, KCNJ8 P4HTM 2204/4885HPGDS 1223/4885CHEK2 1202/4885
US-20210347773-A1 ACTIVATOR OF TREK (TWIK RELATED K+ CHANNELS) CHANNELS KCNJ11, KCNJ1, KCNJ8 P4HTM 2204/4885HPGDS 1223/4885CHEK2 1202/4885

“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.