SCHEMBL995828

SCHEMBL995828

NC(=O)c1ccccc1-c1nccs1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSNK1A1 P48729 1/20 0.50
TYRO3 Q06418 1/20 0.50
DYRK1B Q9Y463 1/20 0.50
BCAT2 O15382 2/20 0.49
PDPK1 O15530 1/20 0.46
NUDT1 P36639 1/20 0.44
CHEK2 O96017 1/20 0.44
ADORA2A P29274 1/20 0.43
ADORA1 P30542 1/20 0.43
ALDH1A1 P00352 3/20 0.43
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
GAA P10253 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.43
GRM5 P41594 1/20 0.43
MAPT P10636 2/20 0.42
MEN1 O00255 1/20 0.42
MAPK1 P28482 1/20 0.42
KMT2A Q03164 1/20 0.42
TYK2 P29597 1/20 0.41

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
SCHEMBL30517722 1.00 CSNK1A1 (0.50) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
Hydrochloric Acid SCHEMBL30810223 0.98 CSNK1A1 (0.49) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
SCHEMBL918767 0.94 CSNK1A1 (0.48) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
Pyrrole SCHEMBL11072397 0.91 CSNK1A1 (0.50) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
SCHEMBL919208 0.90 CSNK1A1 (0.44) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
Nitrobenzene SCHEMBL27714783 0.87 MAPT (0.43) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
SCHEMBL27744970 0.86 TYK2 (0.41) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
SCHEMBL27599253 0.86 TYK2 (0.41) CSNK1A1TYRO3DYRK1BBCAT2PDPK1
SCHEMBL5698661 0.85 CYP1A2 (0.53) PDPK1ADORA2AADORA1ALDH1A1NPC1
SCHEMBL2733045 0.84 TYK2 (0.43) CSNK1A1TYRO3DYRK1BPDPK1CHEK2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-120058701-A Thioether structure-containing targeted PHGDH active molecular probe, preparation method and application thereof 中国药科大学 2025-05-30 CN claimed
CN-108602827-A Imidazopyrazine inhibitors of Bruton's tyrosine kinase 安塞塔制药公司 2018-09-28 CN claimed
EP-3256449-A2 SODIUM CHANNEL BLOCKERS Daewoong Pharmaceutical Co., Ltd. (KR) 2017-12-20 EP claimed
WO-2016129933-A2 SODIUM CHANNEL BLOCKERS DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2016-08-18 WO claimed
WO-2016004305-A2 INHIBITORS OF BRUTON'S TYROSINE KINASE PHARMACYCLICS LLC (US) 2016-01-07 WO claimed
EP-2925322-A1 INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL Merck Sharp & Dohme Corp. (US) 2015-10-07 EP claimed
CN-103930409-A Aromatic amidothiazoles, cosmetic or dermatological preparations containing said aromatic amidothiazoles, and use thereof to combat or prevent undesired pigmentation of the skin BEIERSDORF AG 2014-07-16 CN claimed
WO-2014085210-A1 INHIBITORS OF THE RENAL OUTER MEDULLARY POTASSIUM CHANNEL MERCK SHARP & DOHME CORP. (US) 2014-06-05 WO claimed
CN-103070876-A Composition for resisting Japanese encephalitis virus infection and application thereof SHANGHAI VETERINARY RES INST CAAS 2013-05-01 CN claimed
EP-2459554-A2 SUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS Cadila Healthcare Limited (IN) 2012-06-06 EP claimed
EP-2445908-A1 DISUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS Cadila Healthcare Limited (IN) 2012-05-02 EP claimed
CN-102335171-A Application of N-(2-thiazole)benzamide derivatives SHANGHAI VETERINARY RES INST CAAS 2012-02-01 CN claimed
WO-2011013141-A2 SUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS CADILA HEALTHCARE LIMITED (IN) 2011-02-03 WO claimed
WO-2011011514-A1 HETEROARYL BENZAMIDES, COMPOSITIONS AND METHODS OF USE THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2011-01-27 WO claimed
WO-2010150280-A1 DISUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS CADILA HEALTHCARE LIMITED (IN) 2010-12-29 WO claimed
EP-2086964-A2 BENZOYL AMINO HETEROCYCLYL COMPOUNDS USEFUL IN THE TREATMENT OF A DISEASE MEDIATED THROUGH GLK Astra Zeneca AB (SE) 2009-08-12 EP claimed
WO-2008050101-A2 BENZOYL AMINO HETEROCYCLYL COMPOUNDS USEFUL IN THE TREATMENT OF A DISEASE MEDIATED THROUGH GLK ASTRAZENECA AB (SE) 2008-05-02 WO claimed
EP-1756076-A1 HETROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES AstraZeneca AB (SE) 2007-02-28 EP claimed
WO-2005121110-A1 HETROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES ASTRAZENECA AB (SE) 2005-12-22 WO claimed
EP-4583870-A2 MITOCHONDRIAL UNCOUPLERS FOR TREATMENT OF METABOLIC DISEASES AND CANCER Mito Biopharma, LLC (US) 2025-07-16 EP disclosed
CN-120058701-A Thioether structure-containing targeted PHGDH active molecular probe, preparation method and application thereof 中国药科大学 2025-05-30 CN disclosed
WO-2024054766-A2 MITOCHONDRIAL UNCOUPLERS FOR TREATMENT OF METABOLIC DISEASES AND CANCER MITO BIOPHARMA, LLC (US) 2024-03-14 WO disclosed
EP-4308122-A1 HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS Chiesi Farmaceutici S.p.A. (IT) 2024-01-24 EP disclosed
WO-2022194779-A1 HETEROCYCLIC DERIVATIVES AS JANUS KINASE INHIBITORS CHIESI FARMACEUTICI S.P.A. (IT) 2022-09-22 WO disclosed
US-20210380546-A1 VACCINE ADJUVANT THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2021-12-09 US disclosed
CN-106632401-B Methods and compounds for the synthesis of fused aminodihydrothiazine derivatives 卫材R&D管理有限公司 2020-12-29 CN disclosed
CN-110167556-A Thio-hydantoin androgen receptor antagonist for treating cancer 詹森药业有限公司 2019-08-23 CN disclosed
CN-110023290-A heteroaryl carboxamide compounds as RIPK2 inhibitors 勃林格殷格翰国际有限公司 2019-07-16 CN disclosed
CN-109640986-A Thio-hydantoin androgen receptor antagonists for treating cancer 詹森药业有限公司 2019-04-16 CN disclosed
US-10196411-B2 Tizoxanide phosphate and alkane sulfonate and pharmaceutical applications thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2019-02-05 US disclosed
EP-3006431-B1 TIZOXANIDE CARBAMATE AND PHARMACEUTICAL USE THEREOF INST PHARMACOLOGY & TOXICOLOGY ACADEMY MILITARY MEDICAL SCIENCES PLA CHINA (CN) 2019-01-30 EP disclosed
CN-108938629-A The application of 3- methyl-N- (4- Trifluoromethoxyphen-l) benzimidazole and thiazole carboxamides 马韫韬 2018-12-07 CN disclosed
CN-108853098-A The application of N- (2- furfuryl) -3- tolimidazole and thiazole carboxamides 山东大学齐鲁医院 2018-11-23 CN disclosed
US-10131643-B2 Tizoxanide carbamate and pharmaceutical use thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2018-11-20 US disclosed
CN-105030797-B The composition of a kind of anti-japanese encephalitis virus infection and its application 中国农业科学院上海兽医研究所 2018-10-23 CN disclosed
CN-105030797-B The composition of a kind of anti-japanese encephalitis virus infection and its application 中国农业科学院上海兽医研究所 2018-10-23 CN disclosed
CN-108685912-A The application of N- (the bromo- 2- methoxyphenyls of 5-) benzimidazoles and thiazole carboxamides 山东大学 2018-10-23 CN disclosed
CN-108602827-A Imidazopyrazine inhibitors of Bruton's tyrosine kinase 安塞塔制药公司 2018-09-28 CN disclosed
US-20170362261-A1 Tizoxanide Phosphate and Alkane Sulfonate and Pharmaceutical Applications Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2017-12-21 US disclosed
EP-3239160-A1 TIZOXANIDE PHOSPHATE AND ALKANE SULFONATE AND PHARMACEUTICAL APPLICATIONS THEREOF Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2017-11-01 EP disclosed
CN-106632401-A Methods and compounds for the synthesis of fused aminodihydrothiazine derivatives 卫材R&D管理有限公司 2017-05-10 CN disclosed
US-20160340326-A1 Tizoxanide Carbamate and Pharmaceutical Use Thereof INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY ACADEMY OF MILITARY MEDICAL SCIENCES P.L.A. CHINA (CN) 2016-11-24 US disclosed
US-9447033-B2 Potassium channel blockers JAPAN TOBACCO INC. (JP) 2016-09-20 US disclosed
EP-3006431-A1 TIZOXANIDE CARBAMATE AND PHARMACEUTICAL USE THEREOF Institute of Pharmacology and Toxicology Academy of Military Medical Sciences P.L.A. China (CN) 2016-04-13 EP disclosed
WO-2016004305-A2 INHIBITORS OF BRUTON'S TYROSINE KINASE PHARMACYCLICS LLC (US) 2016-01-07 WO disclosed
WO-2016004272-A1 INHIBITORS OF BRUTON'S TYROSINE KINASE PHARMACYCLICS LLC (US) 2016-01-07 WO disclosed
US-20150259282-A1 Potassium Channel Blockers XENTION LIMITED (GB) 2015-09-17 US disclosed
US-9120762-B2 Salts of bicyclo-substituted pyrazolon azo derivatives, preparation method and use thereof JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2015-09-01 US disclosed
US-9073834-B2 Potassium channel blockers XENTION LIMITED (GB) 2015-07-07 US disclosed
EP-2236500-B1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF JIANGSU HENGRUI MEDICINE CO (CN) 2014-12-24 EP disclosed
US-20140221337-A1 Potassium Channel Blockers XENTION LIMITED (GB) 2014-08-07 US disclosed
CN-103930409-A Aromatic amidothiazoles, cosmetic or dermatological preparations containing said aromatic amidothiazoles, and use thereof to combat or prevent undesired pigmentation of the skin BEIERSDORF AG 2014-07-16 CN disclosed
US-20140140953-A1 SALTS OF BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION METHOD AND USE THEREOF SHANGHAI HENGRUI PHARMACEUTICAL CO., LTD. (CN) 2014-05-22 US disclosed
US-8673901-B2 Potassium channel blockers XENTION LIMITED (GB) 2014-03-18 US disclosed
US-8642637-B2 Salts of bicyclo-substituted pyrazolon azo derivatives, preparation method and use thereof JIANGSU HENGRUI MEDICINE CO., LTD. (CN) 2014-02-04 US disclosed
CN-103502231-A Methods and compounds for the synthesis of fused aminodihydrothiazine derivatives EISAI R&D MAN CO LTD 2014-01-08 CN disclosed
CN-102335171-B Application of N-(2-thiazole)benzamide derivatives SHANGHAI VETERINARY RES INST CAAS 2013-09-11 CN disclosed
CN-101679242-B Ethylidene hydrazine carboxamide derivatives, preparation process and pharmaceutical use thereof SHANGHAI HENGRUI PHARM CO LTD 2013-07-10 CN disclosed
US-20130123507-A1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF SHANGHAI HENGRUI PHARMACEUTICAL CO. LTD. (CN) 2013-05-16 US disclosed
CN-103070876-A Composition for resisting Japanese encephalitis virus infection and application thereof SHANGHAI VETERINARY RES INST CAAS 2013-05-01 CN disclosed
US-8367710-B2 Bicyclo-substituted pyrazolon azo derivatives, preparation process and pharmaceutical use thereof JIANGSU HENGRUI MEDICINE CO. LTD. (CN) 2013-02-05 US disclosed
CN-102159217-B Salt of bicyclo-substituted pyrazolone azo derivative, preparation method and application thereof JIANGSU HENGRUI MEDICINE CO 2012-10-03 CN disclosed
US-20120164102-A1 SALTS OF BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION METHOD AND USE THEREOF SHANGHAI HENGRUI PHARMACEUTICAL CO., LTD. (CN) 2012-06-28 US disclosed
EP-2459554-A2 SUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS Cadila Healthcare Limited (IN) 2012-06-06 EP disclosed
EP-2445908-A1 DISUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS Cadila Healthcare Limited (IN) 2012-05-02 EP disclosed
EP-2441457-A1 SALTS OF BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION METHOD AND USE THEREOF Jiangsu Hengrui Medicine Co., Ltd. (CN) 2012-04-18 EP disclosed
CN-102335171-A Application of N-(2-thiazole)benzamide derivatives SHANGHAI VETERINARY RES INST CAAS 2012-02-01 CN disclosed
CN-101679286-B Bicyclo-substituted pyrazolon azo derivatives, preparation process and pharmaceutical use thereof JIANGSU HENGRUI MEDICINE CO 2011-06-08 CN disclosed
WO-2011013141-A2 SUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS CADILA HEALTHCARE LIMITED (IN) 2011-02-03 WO disclosed
WO-2011011514-A1 HETEROARYL BENZAMIDES, COMPOSITIONS AND METHODS OF USE THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2011-01-27 WO disclosed
WO-2010150280-A1 DISUBSTITUTED BENZAMIDE DERIVATIVES AS GLUCOKINASE (GK) ACTIVATORS CADILA HEALTHCARE LIMITED (IN) 2010-12-29 WO disclosed
CN-101928281-A Bicyclo-substituted pyrazolone azo derivative, preparation method thereof and application thereof in medicaments SHANGHAI HENGRUI PHARM CO LTD 2010-12-29 CN disclosed
CN-101921232-A Salt of 2-ring substituted pyrazolone azo derivatives, and preparation method and application thereof in medicaments SHANGHAI HENGRUI PHARM CO LTD 2010-12-22 CN disclosed
US-20100316601-A1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF JIANGSU HENGRUI MEDICINE CO. LTD. (CN) 2010-12-16 US disclosed
EP-2236500-A1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF Jiangsu Hengrui Medicine Co., Ltd. (CN) 2010-10-06 EP disclosed
EP-2178852-A1 ALKYLSULFONYL-SUBSTITUTED THIAZOLIDE COMPOUNDS Romark Laboratories, L.C. (US) 2010-04-28 EP disclosed
US-20100087428-A1 Novel Potassium Channel Blockers XENTION LIMITED (GB) 2010-04-08 US disclosed
CN-101679242-A Ethylene hydrazine amide derivative, preparation method and medical application thereof SHANGHAI HENGRUI PHARM CO LTD 2010-03-24 CN disclosed
CN-101679286-A Bicyclic substituted pyrazolone azo derivative, preparation method thereof and application thereof in medicine SHANGHAI HENGRUI PHARM CO LTD 2010-03-24 CN disclosed
WO-2009114552-A1 HETEROARYL COMPOUNDS, COMPOSITIONS, AND METHODS OF USE IN CANCER TREATMENT THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2009-09-17 WO disclosed
CN-101514179-A Indolone hydrazine ethylidene carbonyl compound, method for preparing same and application thereof in medicine SHANGHAI HENGRUI PHARM CO LTD (CN) 2009-08-26 CN disclosed
EP-2086964-A2 BENZOYL AMINO HETEROCYCLYL COMPOUNDS USEFUL IN THE TREATMENT OF A DISEASE MEDIATED THROUGH GLK Astra Zeneca AB (SE) 2009-08-12 EP disclosed
CN-101481352-A Bicycle substituted pyrazolone azo derivative, preparation thereof and use in medicine SHANGHAI HENGRUI PHARM CO LTD (CN) 2009-07-15 CN disclosed
US-20090088371-A1 COMBINATION THERAPY WITH SYK KINASE INHIBITOR RIGEL PHARMACEUTICALS, INC. 2009-04-02 US disclosed
WO-2009035788-A1 ALKYLSULFONYL-SUBSTITUTED THIAZOLIDE COMPOUNDS ROMARK LABORATORIES L.C. (US) 2009-03-19 WO disclosed
WO-2009029682-A1 COMBINATION THERAPY WITH SYK KINASE INHIBITOR RIGEL PHARMACEUTICALS, INC. (US) 2009-03-05 WO disclosed
CN-100420678-C Cyclization process for substituted benzothiazole derivatives HOFFMANN LA ROCHE (CH) 2008-09-24 CN disclosed
WO-2008050101-A2 BENZOYL AMINO HETEROCYCLYL COMPOUNDS USEFUL IN THE TREATMENT OF A DISEASE MEDIATED THROUGH GLK ASTRAZENECA AB (SE) 2008-05-02 WO disclosed
EP-1828153-A1 N-(2-AMINOPHENYL)-4-(5-((ETHYLAMINO)METHYL)-1,3-THIAZOL-2-YL)BENZAMIDE AND N-(2-AMINOPHENYL)-4-(5-((ISOPROPYLAMINO)METHYL)-1,3-THIAZOL-2-YL)BENZAMIDE AS HDAC INHIBITORS AstraZeneca AB (SE) 2007-09-05 EP disclosed
US-7241783-B2 Thrombopoietin mimetics SMITHKLINE BEECHAM CORPORATION (US) 2007-07-10 US disclosed
EP-1756076-A1 HETROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES AstraZeneca AB (SE) 2007-02-28 EP disclosed
CN-1870996-A N-thiazol-2-yl-benzamide derivatives LUNDBECK & CO AS H (DK) 2006-11-29 CN disclosed
WO-2006064246-A1 N- (2-AMINOPHENYL) -4- (5- ((ETHYLAMINO) METHYL) 1,3-THIAZOL-2-YL) BENZAMIDE AND N- (2-AMINOPHEYNL) -4- (5- ((ISOPROPYLAMINO) METHYL) -1,3-THIAZOL-2-YL) BENZAMIDE AS HDAC INHIBITORS ASTRAZENECA AB (SE) 2006-06-22 WO disclosed
EP-1656373-A2 DERIVATIVES OF 2-ACYLAMINO-4-PHENYLTHIAZOLE, PREPARATION METHOD THEREOF AND USE OF SAME AS CHEMOKINEANTAGONISTS Sanofi-Aventis (FR) 2006-05-17 EP disclosed
CN-1738808-A Cyclization process for substituted benzothiazole derivatives HOFFMANN LA ROCHE (CH) 2006-02-22 CN disclosed
WO-2005121110-A1 HETROARYL BENZAMIDE DERIVATIVES FOR USE AS GLK ACTIVATORS IN THE TREATMENT OF DIABETES ASTRAZENECA AB (SE) 2005-12-22 WO disclosed
EP-1583752-A2 CYCLIZATION PROCESS FOR SUBSTITUTED BENZOTHIAZOLE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2005-10-12 EP disclosed
EP-1349613-A4 THROMBOPOIETIN MIMETICS SMITHKLINE BEECHAM CORP (US) 2005-09-21 EP disclosed
WO-2004096798-A2 DERIVATIVES OF 2-ACYLAMINO-4-PHENYLTHIAZOLE, PREPARATION METHOD THEREOF AND USE OF SAME AS CHEMOKINE ANTAGONISTS SANOFI-AVENTIS (FR) 2004-11-11 WO disclosed
WO-2004060879-A2 CYCLIZATION PROCESS FOR SUBSTITUTED BENZOTHIAZOLE DERIVATIVES F. HOFFMANN-LA ROCHE AG (CH) 2004-07-22 WO disclosed
US-20040058990-A1 Thrombopoietin mimetics SMITHKLINE BEECHAM CORPORATION 2004-03-25 US disclosed
EP-1349613-A2 THROMBOPOIETIN MIMETICS SmithKline Beecham Corporation (US) 2003-10-08 EP disclosed
EP-0871619-B1 PHENYL THIAZOLE DERIVATIVES WITH ANTI HERPES VIRUS PROPERTIES BOEHRINGER INGELHEIM PHARMA (US) 2002-11-06 EP disclosed
US-6458959-B1 VIRICIDES AND ENZYME INHIBITORS BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. 2002-10-01 US disclosed
WO-2002049413-A2 THROMBOPOIETIN MIMETICS SMITHKLINE BEECHAM CORPORATION (US) 2002-06-27 WO disclosed
US-6348477-B1 SUBSTITUTED PHENYL THIAZOLE DERIVATIVES AS VIRICIDES BOEHRINGER INGELHEIM(CANADA) LTD. (CA) 2002-02-19 US disclosed
US-6057451-A AMINOTHIAZOLE DERIVATIVES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 2000-05-02 US disclosed
CN-1207094-A Phenyl thiazole derivatives with anti herpes virus properties BOEHRINGER INGELHEIM PHARMA (US) 1999-02-03 CN disclosed
EP-0871619-A1 PHENYL THIAZOLE DERIVATIVES WITH ANTI HERPES VIRUS PROPERTIES BOEHRINGER INGELHEIM PHARMACEUTICALS INC. (US) 1998-10-21 EP disclosed
WO-1997024343-A1 PHENYL THIAZOLE DERIVATIVES WITH ANTI HERPES VIRUS PROPERTIES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 1997-07-10 WO disclosed
WO-1997024343-A1 PHENYL THIAZOLE DERIVATIVES WITH ANTI HERPES VIRUS PROPERTIES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 1997-07-10 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 (14 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-20130123507-A1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF THPO, MPL, TEK CSNK1A1 1147/4885TYRO3 46/4885DYRK1B 1717/4885
US-10131643-B2 Tizoxanide carbamate and pharmaceutical use thereof CYP2C9, CA9, CYP3A7 CSNK1A1 653/4885TYRO3 1967/4885DYRK1B 1879/4885
US-20160340326-A1 Tizoxanide Carbamate and Pharmaceutical Use Thereof CYP2C9, CA9, CYP3A7 CSNK1A1 653/4885TYRO3 1967/4885DYRK1B 1879/4885
US-20040058990-A1 Thrombopoietin mimetics MPL, THPO, TEK CSNK1A1 4766/4885TYRO3 450/4885DYRK1B 2642/4885
US-20100316601-A1 BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION PROCESS AND PHARMACEUTICAL USE THEREOF THPO, MPL, TEK CSNK1A1 1147/4885TYRO3 46/4885DYRK1B 1717/4885
US-20140221337-A1 Potassium Channel Blockers KCNJ2, KCNH2, KCNB1 CSNK1A1 1343/4885TYRO3 2812/4885DYRK1B 1758/4885
US-10196411-B2 Tizoxanide phosphate and alkane sulfonate and pharmaceutical applications thereof TPI1, ALK, STS CSNK1A1 856/4885TYRO3 378/4885DYRK1B 424/4885
US-20100087428-A1 Novel Potassium Channel Blockers HCN4, SCN2B, KCNH2 CSNK1A1 1327/4885TYRO3 592/4885DYRK1B 2320/4885
US-20210380546-A1 VACCINE ADJUVANT IFNG, TLR9, LY96 CSNK1A1 3541/4885TYRO3 2234/4885DYRK1B 4737/4885
US-20090088371-A1 COMBINATION THERAPY WITH SYK KINASE INHIBITOR MPL, SYK, BTK CSNK1A1 775/4885TYRO3 12/4885DYRK1B 259/4885
US-20150259282-A1 Potassium Channel Blockers KCNJ2, KCNH2, KCNB1 CSNK1A1 1343/4885TYRO3 2812/4885DYRK1B 1758/4885
US-20140140953-A1 SALTS OF BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION METHOD AND USE THEREOF THPO, MPL, TEK CSNK1A1 1184/4885TYRO3 34/4885DYRK1B 1447/4885
US-20170362261-A1 Tizoxanide Phosphate and Alkane Sulfonate and Pharmaceutical Applications Thereof TPI1, ALK, STS CSNK1A1 856/4885TYRO3 378/4885DYRK1B 424/4885
US-20120164102-A1 SALTS OF BICYCLO-SUBSTITUTED PYRAZOLON AZO DERIVATIVES, PREPARATION METHOD AND USE THEREOF THPO, MPL, TEK CSNK1A1 1184/4885TYRO3 34/4885DYRK1B 1447/4885

“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.