SCHEMBL655335

SCHEMBL655335

CC(=O)c1ccc(OBOc2ccc(C(C)=O)cc2)cc1

nearest known ligand 0.64

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
MAPT P10636 5/20 0.64
HPGD P15428 2/20 0.64
RAB9A P51151 1/20 0.64
L3MBTL1 Q9Y468 2/20 0.55
GAA P10253 1/20 0.53
STS P08842 1/20 0.52
LMNA P02545 3/20 0.50
NPSR1 Q6W5P4 2/20 0.50
POLB P06746 1/20 0.50
MAOB P27338 5/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
KMT2A Q03164 4/20 0.46
GLA P06280 1/20 0.46
TSHR P16473 1/20 0.46
ALDH1A1 P00352 1/20 0.46
HSD17B1 P14061 1/20 0.45
MAOA P21397 1/20 0.44

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
SCHEMBL12565754 0.84 MAPT (0.61) MAPTHPGDRAB9AL3MBTL1GAA
SCHEMBL210295 0.79 CA1 (0.58) LMNASMN1; SMN2KMT2ATSHRALDH1A1
SCHEMBL151953 0.78 CA1 (0.67) MAPTRAB9ASTSSMN1; SMN2KMT2A
SCHEMBL3301210 0.78 HPGD (1.00) MAPTHPGDRAB9AL3MBTL1GAA
SCHEMBL203697 0.78 HPGD (1.00) MAPTHPGDRAB9AL3MBTL1GAA
SCHEMBL540837 0.77 PARP10 (0.64) KMT2AALDH1A1
SCHEMBL50646 0.77 MAPT (0.68) MAPTHPGDRAB9AL3MBTL1GAA
SCHEMBL3291543 0.77 SMN1; SMN2 (0.50) MAPTHPGDRAB9AL3MBTL1GAA
SCHEMBL177478 0.77 HPGD (0.68) MAPTHPGDRAB9AMAOBSMN1; SMN2
SCHEMBL289656 0.77 KMT2A (0.57) RAB9AL3MBTL1MAOBSMN1; SMN2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260034127-A1 TREATMENT OF GVHD KADMON CORP LLC (FR) 2026-02-05 US disclosed
EP-4658656-A1 CONDENSED HETEROCYCLIC COMPOUNDS AS INHIBITOR OF DIACYLGLYCEROL KINASES Beone Medicines I GmbH (CH) 2025-12-10 EP disclosed
US-20250282735-A1 BICYCLE COMPOUNDS AS TEAD INHIBITOR DONG-A ST CO., LTD. (KR) 2025-09-11 US disclosed
CN-120040450-A Crystalline forms of a phosphoinositide 3 kinase (PI 3K) inhibitor 因赛特公司 2025-05-27 CN disclosed
CN-114555594-B Substituted azacycles as TRMP modulators 奇华顿股份有限公司 2025-03-18 CN disclosed
CN-115210233-B 1,3, 4-Oxadiazole derivative compounds as histone deacetylase 6 inhibitors and pharmaceutical compositions containing the same 株式会社钟根堂 2025-02-14 CN disclosed
EP-4233864-B1 COMPOSITION COMPRISING AN INDOLIZINE DERIVATIVE AND A CYCLIC DINUCLEOTIDE AS ACTIVE AGENTS UNIV AJOU IND ACADEMIC COOP FOUND (KR) 2025-02-12 EP disclosed
CN-113677683-B Crystalline forms of a phosphoinositide 3 kinase (PI 3K) inhibitor 因赛特公司 2025-01-14 CN disclosed
US-20240400555-A1 Compounds, Compositions and Methods for Attenuation of Mammalian Translation of C-MYC or N-MYC Proteins of the MYC Proto-Oncogene Family of BHLH Transcription Factors INITIAL THERAPEUTICS, INC. (US) 2024-12-05 US disclosed
US-20240400559-A1 SOLID STATE EMITTERS BASED ON PYRIDINIUM SCAFFOLDS COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2024-12-05 US disclosed
WO-2003006151-A1 MICROENCAPSULATED CATALYST, METHODS OF PREPARATION AND METHODS OF USE THEREOF AVECIA LIMITED (GB) 2003-01-23 WO disclosed
WO-2003005971-A2 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. (US) 2003-01-23 WO disclosed
WO-2003002733-A2 COMPOSITIONS FOR ENHANCED CATALYZED REPORTER DEPOSITION PERKINELMER LIFE SCIENCES, INC. (US) 2003-01-09 WO disclosed
EP-1254101-A1 PROPIONIC ACID DERIVATIVES AND THEIR USE IN THE TREATMENT OF DIABETES AND OBESITY Novo Nordisk A/S (DK) 2002-11-06 EP disclosed
WO-2002072031-A2 SUBSTITUTED TETRACYCLINE COMPOUNDS AS SYNERGISTIC ANTIFUNGAL AGENTS PARATEK PHARMACEUTICALS, INC. (US) 2002-09-19 WO disclosed
WO-2002070507-A2 GLYCORTICOID RECEPTOR ANTAGONISTS FOR TREATMENT OF DIABETES ABBOTT LABORATORIES (US) 2002-09-12 WO disclosed
WO-2002055497-A1 ARYL PIPERIDINE DERIVATIVES AS INDUCERS OF LDL-RECEPTOR EXPRESSION GLAXO GROUP LIMITED (GB) 2002-07-18 WO disclosed
WO-2002055495-A1 ARYL PIPERIDINE DERIVATIVES AS INDUCERS OF LDL-RECEPTOR EXPRESSION GLAXO GROUP LIMITED (GB) 2002-07-18 WO disclosed
US-20010041802-A1 Glucocorticoid receptor antagonists for treatment of diabetes KARO BIO AB (SE) 2001-11-15 US disclosed
WO-2001055085-A1 PROPIONIC ACID DERIVATIVES AND THEIR USE IN THE TREATMENT OF DIABETES AND OBESITY NOVO NORDISK A/S (DK) 2001-08-02 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 (5 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-20260034127-A1 TREATMENT OF GVHD ROCK2, RHOA, MYH2 MAPT 2222/4885HPGD 2763/4885RAB9A 458/4885
US-20010041802-A1 Glucocorticoid receptor antagonists for treatment of diabetes NR3C1, GPR119, NR3C2 MAPT 4638/4885HPGD 1024/4885RAB9A 4602/4885
US-20250282735-A1 BICYCLE COMPOUNDS AS TEAD INHIBITOR TEAD1, TEAD2, TEAD3 MAPT 34/4885HPGD 135/4885RAB9A 952/4885
US-20240400559-A1 SOLID STATE EMITTERS BASED ON PYRIDINIUM SCAFFOLDS CYB5R3, NQO1, SQOR MAPT 2160/4885HPGD 593/4885RAB9A 4185/4885
US-20240400555-A1 Compounds, Compositions and Methods for Attenuation of Mammalian Translation of C-MYC or N-MYC Proteins of the MYC Proto-Oncogene Family of BHLH Transcription Factors MYCBP, MYC, MYCBP2 MAPT 2934/4885HPGD 2082/4885RAB9A 3390/4885

“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.