SCHEMBL20181613

SCHEMBL20181613

CCc1nc2ncccn2c1C(=O)c1ccc(OC)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.50
KDM4E B2RXH2 5/20 0.50
HPGD P15428 2/20 0.50
HSD17B10 Q99714 1/20 0.50
NPC1 O15118 3/20 0.46
RAB9A P51151 3/20 0.46
PKM P14618 1/20 0.45
LMNA P02545 4/20 0.44
ALOX15 P16050 2/20 0.44
NPSR1 Q6W5P4 1/20 0.44
MAPT P10636 2/20 0.42
MEN1 O00255 1/20 0.42
RECQL P46063 1/20 0.42
KMT2A Q03164 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
HTT P42858 1/20 0.42
GAA P10253 2/20 0.42
POLB P06746 2/20 0.41
CYP19A1 P11511 1/20 0.40
VNN1 O95497 1/20 0.40

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
SCHEMBL22623348 0.88 ALDH1A1 (0.40) ALDH1A1KDM4EHPGDHSD17B10NPC1
SCHEMBL20181614 0.87 ALDH1A1 (0.50) ALDH1A1KDM4EHPGDHSD17B10RAB9A
SCHEMBL21192147 0.84 KDM4E (0.48) ALDH1A1KDM4EHPGDHSD17B10PKM
SCHEMBL22623459 0.83 LMNA (0.43) ALDH1A1KDM4EHPGDRAB9ALMNA
SCHEMBL21176899 0.83 KDM4E (0.45) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL29638921 0.83 KDM4E (0.45) ALDH1A1KDM4EHPGDHSD17B10LMNA
SCHEMBL18629838 0.81 SMN1; SMN2 (0.52) ALDH1A1KDM4EHPGDHSD17B10NPC1
SCHEMBL21191884 0.80 ALDH1A1 (0.43) ALDH1A1KDM4EHPGDHSD17B10NPC1
SCHEMBL21191881 0.80 KDM4E (0.48) ALDH1A1KDM4EHPGDHSD17B10MAPT
SCHEMBL29638909 0.80 ALDH1A1 (0.43) ALDH1A1KDM4EHPGDHSD17B10NPC1

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-RE50083-E1 URAT1 inhibitor and use thereof JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO., LTD. (CN) 2024-08-20 US disclosed
CN-117586272-A Heterocyclic compound, preparation method and application thereof in medicine 苏州信诺维医药科技股份有限公司 2024-02-23 CN disclosed
CN-111615515-B Heterocyclic compound, preparation method and application thereof in medicine 苏州信诺维医药科技股份有限公司 2023-11-24 CN disclosed
EP-3741759-B1 IMIDAZO[1,2-A]PYRIMIDINE AND IMIDAZO[1,2-C]PYRIMIDINE COMPOUNDS AND USE THEREOF IN THE TREATMENT OF HYPERURICEMIA AND GOUT EVOPOINT BIOSCIENCES CO LTD (CN) 2023-08-23 EP disclosed
US-11453674-B2 Heterocyclic compound, preparation method and use thereof in medicine Evopoint Biosciences Co., Ltd. (CN) 2022-09-27 US disclosed
EP-3543240-B1 URAT1 INHIBITOR AND USE THEREOF JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO LTD (CN) 2022-07-06 EP disclosed
EP-3543240-B1 URAT1 INHIBITOR AND USE THEREOF JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO LTD (CN) 2022-07-06 EP disclosed
CN-112979661-B Heterocyclic compound, preparation method and application thereof in medicine 苏州信诺维医药科技股份有限公司 2022-05-17 CN disclosed
US-10875865-B2 URAT1 inhibitor and use thereof JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO., LTD. (CN) 2020-12-29 US disclosed
US-10875865-B2 URAT1 inhibitor and use thereof JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO., LTD. (CN) 2020-12-29 US disclosed
EP-3741759-A1 HETEROCYCLIC COMPOUND, PREPARATION METHOD AND USE THEREOF IN MEDICINE Suzhou Sinovent Pharmaceuticals Co., Ltd. (CN) 2020-11-25 EP disclosed
US-20200347070-A1 HETEROCYCLIC COMPOUND, PREPARATION METHOD AND USE THEREOF IN MEDICINE SHANGHAI PUCHI BIOMEDICAL CO., LTD. (CN) 2020-11-05 US disclosed
US-20200347070-A1 HETEROCYCLIC COMPOUND, PREPARATION METHOD AND USE THEREOF IN MEDICINE SHANGHAI PUCHI BIOMEDICAL CO., LTD. (CN) 2020-11-05 US disclosed
US-20200062763-A1 URAT1 INHIBITOR AND USE THEREOF JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO., LTD. (CN) 2020-02-27 US disclosed
US-20200062763-A1 URAT1 INHIBITOR AND USE THEREOF JIANGSU ATOM BIOSCIENCE AND PHARMACEUTICAL CO., LTD. (CN) 2020-02-27 US disclosed
EP-3543240-A1 URAT1 INHIBITOR AND USE THEREOF Jiangsu Atom Bioscience And Pharmaceutical Co., Ltd. (CN) 2019-09-25 EP disclosed
EP-3543240-A1 URAT1 INHIBITOR AND USE THEREOF Jiangsu Atom Bioscience And Pharmaceutical Co., Ltd. (CN) 2019-09-25 EP disclosed
WO-2018090921-A1 URAT1 INHIBITOR AND USE THEREOF 江苏新元素医药科技有限公司 2018-05-24 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 (4 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-11453674-B2 Heterocyclic compound, preparation method and use thereof in medicine PAH, NLRP3, CYP11B2 ALDH1A1 1562/4885KDM4E 2925/4885HPGD 251/4885
US-20200062763-A1 URAT1 INHIBITOR AND USE THEREOF SLC14A1, SLC10A6, SLC10A1 ALDH1A1 356/4885KDM4E 4224/4885HPGD 2933/4885
US-10875865-B2 URAT1 inhibitor and use thereof SLC14A1, SLC10A6, SLC10A1 ALDH1A1 356/4885KDM4E 4224/4885HPGD 2933/4885
US-20200347070-A1 HETEROCYCLIC COMPOUND, PREPARATION METHOD AND USE THEREOF IN MEDICINE PAH, NLRP3, CYP11B2 ALDH1A1 1562/4885KDM4E 2925/4885HPGD 251/4885

“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.