SCHEMBL232290

SCHEMBL232290

O=C(O)c1cnc(Cl)c(Cl)c1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HCAR2 Q8TDS4 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
TTR P02766 1/20 0.50
TSHR P16473 2/20 0.48
KMT2A Q03164 4/20 0.46
TDP1 Q9NUW8 3/20 0.44
MEN1 O00255 2/20 0.44
ALDH1A1 P00352 1/20 0.44
KDM4E B2RXH2 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
MGAM O43451 1/20 0.44
OPRM1 P35372 1/20 0.43
OPRD1 P41143 1/20 0.43
P4HA1 P13674 1/20 0.43
P4HTM Q9NXG6 1/20 0.43
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43
ALOX15 P16050 1/20 0.43
TPMT P51580 1/20 0.43
SRD5A2 P31213 1/20 0.42

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
SCHEMBL29365646 1.00 HCAR2 (0.50) HCAR2NAPRTTTRTSHRKMT2A
Hydrochloric Acid SCHEMBL7476482 0.98 HCAR2 (0.48) HCAR2NAPRTTTRTSHRKMT2A
Pyridine SCHEMBL5309182 0.89 HCAR2 (0.46) HCAR2NAPRTTTRTSHRKMT2A
SCHEMBL29838220 0.83 KMT2A (0.46) NAPRTKMT2ATDP1MEN1ALDH1A1
SCHEMBL991416 0.83 KMT2A (0.46) NAPRTKMT2ATDP1MEN1ALDH1A1
SCHEMBL3650453 0.81 HCAR2 (0.48) HCAR2NAPRTTTRTSHRKMT2A
SCHEMBL3517645 0.81 HCAR2 (0.48) HCAR2NAPRTTTRKMT2AMEN1
SCHEMBL230989 0.81 KMT2A (0.45) KMT2ATDP1MEN1ALDH1A1KDM4E
SCHEMBL9696266 0.81 TDP1 (0.46) KMT2ATDP1MEN1ALDH1A1KDM4E
SCHEMBL199221 0.81 TTR (0.54) HCAR2NAPRTTTRTSHRKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4661890-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS Purdue Research Foundation (US) 2025-12-17 EP claimed
WO-2024167565-A1 PTP1B/TC-PTP DUAL INHIBITORS AND PROTEIN DEGRADERS PURDUE RESEARCH FOUNDATION (US) 2024-08-15 WO claimed
CN-113912534-B Biphenyl heterocyclic compound, synthesis method and application thereof 江苏科技大学 2023-07-25 CN claimed
WO-2023083161-A1 BIPHENYL HETEROCYCLIC COMPOUND, AND SYNTHESIS METHOD THEREFOR AND USE THEREOF 江苏科技大学 2023-05-19 WO claimed
CN-113980025-B Nicotine and indole hybrid compound, and synthesis method and application thereof 江苏科技大学 2023-02-24 CN claimed
CN-113880847-B Cyclotryptamine alkaloid, and synthesis method and application thereof 江苏科技大学 2023-02-03 CN claimed
CN-115477645-A Alvatripopa maleate series impurities and preparation method and application thereof 湖南先施制药有限公司 2022-12-16 CN claimed
CN-113943947-B Composite film electrode for electrochemical reduction of carbon dioxide and preparation method thereof 浙江工业大学 2022-11-15 CN claimed
CN-115057854-A Preparation method of Alvatripopa maleate intermediate 河北常山生化药业股份有限公司 2022-09-16 CN claimed
CN-113943947-A Composite film electrode for electrochemical reduction of carbon dioxide and preparation method thereof 浙江工业大学 2022-01-18 CN claimed
EP-2697208-A1 1,3 OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS F. Hoffmann-La Roche AG (CH) 2014-02-19 EP claimed
CN-102675196-B Method for preparing 5,6-chloronicotinic acid from 2,3-dichloro-5-trichlorine picoline (DCTC) short steaming residue YANCHENG INST TECHNOLOGY 2014-01-22 CN claimed
WO-2012139993-A1 1,3 OXAZINES AS BACE1 AND/OR BACE2 INHIBITORS F. HOFFMANN-LA ROCHE AG (CH) 2012-10-18 WO claimed
CN-102675196-A Method for preparing 5,6-chloronicotinic acid from 2,3-dichloro-5-trichlorine picoline (DCTC) short steaming residue YANCHENG INST TECHNOLOGY 2012-09-19 CN claimed
US-20120088720-A1 INHIBITORS OF PROTEIN TYROSINE PHOSPHATASES INDIANA UNIVERSITY RESEARCH & TECHNOLOGY CORPORATI (US) 2012-04-12 US claimed
WO-2010118241-A2 INHIBITORS OF PROTEIN TYROSINE PHOSPHATASES INDIANA UNIVERSITY RESEARCH & TECHNOLOGY CORPORATION (US) 2010-10-14 WO claimed
EP-1377589-B1 OXAZOLYL-PYRAZOLE DERIVATIVES AS KINASE INHIBITORS PHARMACIA ITALIA SPA (IT) 2005-09-07 EP claimed
US-5939568-A Accelerated catalysis of olefinic epoxidations THE SCRIPPS RESEARCH INSTITUTE (US) 1999-08-17 US claimed
WO-1998033786-A9 ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS 1998-12-30 WO claimed
WO-1998033786-A1 ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS THE SCRIPPS RESEARCH INSTITUTE (US) 1998-08-06 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20120088720-A1 INHIBITORS OF PROTEIN TYROSINE PHOSPHATASES PTPRCAP, PTPRF, PTPRS HCAR2 4789/4885NAPRT 384/4885TTR 347/4885

“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.