SCHEMBL11794

SCHEMBL11794

Cn1ncc2cc(Br)ccc21

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGFR P00533 1/20 0.46
TRPA1 O75762 1/20 0.45
CTNNB1 P35222 1/20 0.43
TCF7 P36402 1/20 0.43
CDC7 O00311 1/20 0.43
TRPM5 Q9NZQ8 1/20 0.43
MAOB P27338 3/20 0.42
MCL1 Q07820 1/20 0.42
AR P10275 2/20 0.42
APP P05067 1/20 0.41
KMO O15229 1/20 0.41
MAOA P21397 1/20 0.40
ACHE P22303 1/20 0.40
PDE1C Q14123 1/20 0.40
HDAC8 Q9BY41 1/20 0.39
NPC1 O15118 1/20 0.39
ALDH1A1 P00352 1/20 0.39
MAPT P10636 1/20 0.39
HPGD P15428 1/20 0.39
ALOX12 P18054 1/20 0.39

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
SCHEMBL30855622 0.87 EGFR (0.38) EGFRTRPA1CTNNB1TCF7CDC7
SCHEMBL16364359 0.85 TRPA1 (0.51) TRPA1ARAPP
SCHEMBL29427078 0.84 KMO (0.55) EGFRCTNNB1TCF7KMOPDE1C
SCHEMBL422886 0.84 KMO (0.55) EGFRCTNNB1TCF7KMOPDE1C
SCHEMBL424964 0.78 TRPA1 (0.46) TRPA1CTNNB1TCF7CDC7TRPM5
SCHEMBL29769166 0.78 TRPA1 (0.46) TRPA1CTNNB1TCF7CDC7TRPM5
SCHEMBL13137284 0.78 HDAC8 (0.40) EGFRMCL1KMOHDAC8ALDH1A1
SCHEMBL13548 0.77 KMO (0.49) EGFRMCL1KMOHDAC8NPC1
SCHEMBL13106517 0.77 TRPM5 (0.57) CTNNB1TCF7CDC7TRPM5NPC1
SCHEMBL378619 0.76 CHEK1 (0.57) TRPA1CTNNB1TCF7CDC7TRPM5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113912544-B Preparation method of 5-bromo-1-methylindazole 沧州普瑞东方科技有限公司 2023-03-17 CN claimed
CN-113912544-A Preparation method of 5-bromo-1-methylindazole 沧州普瑞东方科技有限公司 2022-01-11 CN claimed
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE MERCK SHARP & DOHME LLC (US) 2026-05-21 US disclosed
US-12617783-B2 Heterocyclic GLP-1R agonists BIOMEA FUSION, INC. (US) 2026-05-05 US disclosed
US-12612379-B2 Inhibitors of APOL1 and methods of using same VERTEX PHARMACEUTICALS INCORPORATED (US) 2026-04-28 US disclosed
US-20260103463-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-04-16 US disclosed
US-20260060961-A1 SUBSTITUTED HETEROCYCLES AS RAS INHIBITORS JAZZ PHARMACEUTICALS IRELAND LTD (IE) 2026-03-05 US disclosed
US-20260055105-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2026-02-26 US disclosed
US-12534452-B2 N-(1H-imidazol-2-yl)benzamide compound and pharmaceutical composition comprising the same as active ingredient KAINOS MEDICINE, INC. (KR) 2026-01-27 US disclosed
US-20260015743-A1 MEDIATED HYDROGEN ANODE FOR USE IN REDUCTIVE ELECTROSYNTHESIS WISCONSIN ALUMNI RES FOUND (US) 2026-01-15 US disclosed
EP-4665718-A1 SMALL MOLECULES AS MONOACYLGLYCEROL LIPASE (MAGL) INHIBITORS, COMPOSITIONS AND USE THEREOF Apogee Pharmaceuticals, Inc. (CA) 2025-12-24 EP disclosed
EP-1477472-A1 SUBSTITUTED PHENYLALKANOIC ACID DERIVATIVE AND USE THEREOF Asahi Kasei Pharma Corporation (JP) 2004-11-17 EP disclosed
US-20040192653-A1 P38 inhibitors and methods of use thereof ARRAY BIOPHARMA INC. 2004-09-30 US disclosed
US-20040180896-A1 P38 inhibitors and methods of use thereof ARRAY BIOPHARMA, INC. 2004-09-16 US disclosed
WO-2004078116-A2 P38 INHIBITORS AND METHODS OF USE THEREOF ARRAY BIOPHARMA, INC. (US) 2004-09-16 WO disclosed
US-20040106611-A1 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC 2004-06-03 US disclosed
CN-1492852-A N-phenylpropylcyclopentyl substituted glutaramide derivatives as NEP inhibitors of FSAD ������ҩ�����޹�˾ 2004-04-28 CN disclosed
US-20040044258-A1 Substituted phenylalkanoic acid derivatives and use thereof ASAHI KASEI PHARMA CORPORATION (JP) 2004-03-04 US disclosed
US-6660756-B2 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC. 2003-12-09 US disclosed
US-20030105132-A1 N-phenpropylcuclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PFIZER INC. 2003-06-05 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 (13 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-12617783-B2 Heterocyclic GLP-1R agonists GLP1R, GIPR, GPR119 EGFR 1414/4885TRPA1 494/4885CTNNB1 631/4885
US-20260015743-A1 MEDIATED HYDROGEN ANODE FOR USE IN REDUCTIVE ELECTROSYNTHESIS HAO2, HACL2, HVCN1 EGFR 1616/4885TRPA1 1810/4885CTNNB1 1058/4885
US-20030105132-A1 N-phenpropylcuclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PREP, ENGASE, ENPEP EGFR 2190/4885TRPA1 4709/4885CTNNB1 4752/4885
US-20260060961-A1 SUBSTITUTED HETEROCYCLES AS RAS INHIBITORS KRAS, NRAS, HRAS EGFR 191/4885TRPA1 3703/4885CTNNB1 78/4885
US-20260138998-A1 GLP-1 RECEPTOR AGONISTS AND METHODS OF USE GLP1R, GIPR, GPR119 EGFR 405/4885TRPA1 671/4885CTNNB1 2692/4885
US-12612379-B2 Inhibitors of APOL1 and methods of using same APOL1, RNASE1, LOXL1 EGFR 363/4885TRPA1 4530/4885CTNNB1 435/4885
US-20040180896-A1 P38 inhibitors and methods of use thereof MAPK1, MAPK3, MAPK8 EGFR 2342/4885TRPA1 3588/4885CTNNB1 4621/4885
US-20260103463-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT GLP1R, GPR119, GIPR EGFR 954/4885TRPA1 625/4885CTNNB1 1624/4885
US-20040044258-A1 Substituted phenylalkanoic acid derivatives and use thereof PTGER1, CYSLTR1, PTGS1 EGFR 3359/4885TRPA1 135/4885CTNNB1 3629/4885
US-20040106611-A1 N-phenpropylcyclopentyl-substituted glutaramide derivatives as inhibitors of neutral endopeptidase PREP, ENGASE, ENPEP EGFR 2509/4885TRPA1 4721/4885CTNNB1 4751/4885
US-20040192653-A1 P38 inhibitors and methods of use thereof MAPK1, MAPK3, MAPK8 EGFR 2342/4885TRPA1 3588/4885CTNNB1 4621/4885
US-20260055105-A1 PYRAZOLOPYRIDINE DERIVATIVE HAVING GLP-1 RECEPTOR AGONIST EFFECT GLP1R, GIPR, GPR119 EGFR 2103/4885TRPA1 332/4885CTNNB1 1863/4885
US-12534452-B2 N-(1H-imidazol-2-yl)benzamide compound and pharmaceutical composition comprising the same as active ingredient IRAK4, IRAK1, IRAK2 EGFR 703/4885TRPA1 1814/4885CTNNB1 3210/4885

“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.