SCHEMBL4290086

SCHEMBL4290086

O=C(O)c1ccc2c(c1)OCCN2

nearest known ligand 0.55

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
MAPT P10636 3/20 0.55
KDM4E B2RXH2 1/20 0.55
ALDH1A1 P00352 3/20 0.50
MAPK1 P28482 1/20 0.50
STAT3 P40763 1/20 0.44
GAA P10253 1/20 0.44
HSD17B10 Q99714 1/20 0.44
PRMT5 O14744 1/20 0.43
WDR77 Q9BQA1 1/20 0.43
NPC1 O15118 2/20 0.43
RAB9A P51151 2/20 0.43
TRPV1 Q8NER1 1/20 0.43
HDAC11 Q96DB2 1/20 0.42
SRD5A2 P31213 1/20 0.41
TSHR P16473 2/20 0.41
ALOX5 P09917 1/20 0.40
PKM P14618 1/20 0.40
CTNNB1 P35222 1/20 0.39
NPSR1 Q6W5P4 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
SCHEMBL29566033 1.00 MAPT (0.55) MAPTKDM4EALDH1A1MAPK1STAT3
SCHEMBL22225992 0.90 MAPT (0.56) MAPTKDM4EALDH1A1MAPK1STAT3
SCHEMBL22227204 0.90 MAPT (0.56) MAPTKDM4EALDH1A1MAPK1STAT3
SCHEMBL20580612 0.87 MAPT (0.56) MAPTKDM4EALDH1A1MAPK1STAT3
Hydrochloric Acid SCHEMBL34474909 0.85 MAPT (0.54) MAPTKDM4EALDH1A1MAPK1STAT3
SCHEMBL29753822 0.85 TSHR (0.60) MAPTKDM4EALDH1A1GAAHSD17B10
SCHEMBL27351890 0.85 PRMT5 (0.43) MAPTKDM4EALDH1A1GAAHSD17B10
SCHEMBL9995863 0.85 TSHR (0.60) MAPTKDM4EALDH1A1GAAHSD17B10
SCHEMBL16560478 0.83 MAPT (0.44) MAPTKDM4EALDH1A1GAAHSD17B10
SCHEMBL3732847 0.83 ALDH1A1 (0.53) MAPTKDM4EALDH1A1MAPK1STAT3

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
US-20240262820-A1 PGDH INHIBITORS AND METHODS OF MAKING AND USING MYOFORTE THERAPEUTICS, INC. 2024-08-08 US disclosed
US-11891389-B2 PGDH inhibitors and methods of making and using MYOFORTE THERAPEUTICS, INC. (US) 2024-02-06 US disclosed
US-20230390274-A1 INHALED FORMULATIONS OF PGDH INHIBITORS AND METHODS OF USE THEREOF MYOFORTE THERAPEUTICS, INC. 2023-12-07 US disclosed
EP-4093385-A1 PGDH INHIBITORS AND METHODS OF MAKING AND USING Myoforte Therapeutics Inc. (US) 2022-11-30 EP disclosed
US-11447493-B2 Inhibitors of cyclin-dependent kinases KINNATE BIOPHARMA INC. 2022-09-20 US disclosed
US-20220267325-A1 PGDH INHIBITORS AND METHODS OF MAKING AND USING MYOFORTE THERAPEUTICS, INC. 2022-08-25 US disclosed
US-11390618-B2 Inhibitors of cyclin-dependent kinases KINNATE BIOPHARMA INC. (US) 2022-07-19 US disclosed
US-11358958-B2 2022-06-14 US disclosed
US-11358958-B2 2022-06-14 US disclosed
US-11345702-B1 PGDH inhibitors and methods of making and using MYOFORTE THERAPEUTICS, INC. (US) 2022-05-31 US disclosed
EP-3121167-A1 COMPOUND BINDING TO PPARG BUT NOT ACTING AS PROMOTER AND PHARMACEUTICAL COMPOSITION FOR TREATING PPARG-RELATED DISEASES CONTAINING SAME AS ACTIVE INGREDIENT Hyundai Pharm Co., Ltd. (KR) 2017-01-25 EP disclosed
US-20160355483-A1 COMPOUND BINDING TO PPARG BUT NOT ACTING AS PROMOTER AND PHARMACEUTICAL COMPOSITION FOR TREATING PPARG-RELATED DISEASES CONTAINING SAME AS ACTIVE INGREDIENT HYUNDAI PHARM CO., LTD. (KR) 2016-12-08 US disclosed
US-20160355483-A1 COMPOUND BINDING TO PPARG BUT NOT ACTING AS PROMOTER AND PHARMACEUTICAL COMPOSITION FOR TREATING PPARG-RELATED DISEASES CONTAINING SAME AS ACTIVE INGREDIENT HYUNDAI PHARM CO., LTD. (KR) 2016-12-08 US disclosed
US-20160355483-A1 COMPOUND BINDING TO PPARG BUT NOT ACTING AS PROMOTER AND PHARMACEUTICAL COMPOSITION FOR TREATING PPARG-RELATED DISEASES CONTAINING SAME AS ACTIVE INGREDIENT HYUNDAI PHARM CO., LTD. (KR) 2016-12-08 US disclosed
US-20090247593-A1 N-THIAZOL-2-YL-BENZAMIDE DERIVATIVES H. LUNDBECK A/S (DK) 2009-10-01 US disclosed
EP-1803455-A1 N-thiazol-2-yl-benzamide derivatives H.Lundbeck A/S (DK) 2007-07-04 EP disclosed
EP-1682129-B1 N-THIAZOL-2-YL-BENZAMIDE DERIVATIVES LUNDBECK & CO AS H (DK) 2007-02-21 EP disclosed
EP-1682129-A1 N-THIAZOL-2-YL-BENZAMIDE DERIVATIVES H. LUNDBECK A/S (DK) 2006-07-26 EP disclosed
US-20060154974-A1 N-thiazol-2-yl-benzamide derivatives H. LUNDBECK A/S (DK) 2006-07-13 US disclosed
WO-2005039572-A1 N-THIAZOL-2-YL-BENZAMIDE DERIVATIVES H. LUNDBECK A/S (DK) 2005-05-06 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 (11 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-20090247593-A1 N-THIAZOL-2-YL-BENZAMIDE DERIVATIVES ADORA2A, ADORA3, ADORA1 MAPT 1300/4885KDM4E 3697/4885ALDH1A1 624/4885
US-11358958-B2 CDK2, CDK1, CDK6 MAPT 1274/4885KDM4E 1178/4885ALDH1A1 3425/4885
US-11891389-B2 PGDH inhibitors and methods of making and using HPGD, HPGDS, PTGS1 MAPT 4693/4885KDM4E 3758/4885ALDH1A1 145/4885
US-20060154974-A1 N-thiazol-2-yl-benzamide derivatives ADORA2A, ADORA3, ADORA1 MAPT 1300/4885KDM4E 3697/4885ALDH1A1 624/4885
US-20220267325-A1 PGDH INHIBITORS AND METHODS OF MAKING AND USING HPGD, HPGDS, PTGS1 MAPT 4693/4885KDM4E 3758/4885ALDH1A1 145/4885
US-11447493-B2 Inhibitors of cyclin-dependent kinases CDK2, CCNK, CDK1 MAPT 2163/4885KDM4E 1278/4885ALDH1A1 3722/4885
US-20240262820-A1 PGDH INHIBITORS AND METHODS OF MAKING AND USING HPGD, HPGDS, PTGS1 MAPT 4762/4885KDM4E 3885/4885ALDH1A1 183/4885
US-20160355483-A1 COMPOUND BINDING TO PPARG BUT NOT ACTING AS PROMOTER AND PHARMACEUTICAL COMPOSITION FOR TREATING PPARG-RELATED DISEASES CONTAINING SAME AS ACTIVE INGREDIENT PPARG, CDK5, CDK5R1 MAPT 1059/4885KDM4E 3079/4885ALDH1A1 2975/4885
US-20230390274-A1 INHALED FORMULATIONS OF PGDH INHIBITORS AND METHODS OF USE THEREOF HPGD, HPGDS, GCDH MAPT 4312/4885KDM4E 2652/4885ALDH1A1 37/4885
US-11345702-B1 PGDH inhibitors and methods of making and using HPGD, HPGDS, PTGS1 MAPT 4693/4885KDM4E 3758/4885ALDH1A1 145/4885
US-11390618-B2 Inhibitors of cyclin-dependent kinases CDK2, CCNK, CDK1 MAPT 2163/4885KDM4E 1278/4885ALDH1A1 3722/4885

“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.