SCHEMBL856236

SCHEMBL856236

CCc1ccc(NCc2ccccc2)cc1

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 3/20 0.69
MEN1 O00255 3/20 0.69
KMT2A Q03164 3/20 0.69
ALDH1A1 P00352 2/20 0.69
MAPT P10636 2/20 0.69
APAF1 O14727 1/20 0.69
USP2 O75604 1/20 0.69
GAA P10253 1/20 0.69
HPGD P15428 1/20 0.69
ALOX15 P16050 1/20 0.69
ALOX12 P18054 1/20 0.69
MAPK1 P28482 1/20 0.69
CASP1 P29466 1/20 0.69
BLM P54132 1/20 0.69
HSD17B10 Q99714 1/20 0.69
L3MBTL1 Q9Y468 1/20 0.69
HTT P42858 1/20 0.68
CXCR4 P61073 1/20 0.59
CA1 P00915 2/20 0.59
CA2 P00918 2/20 0.59

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
SCHEMBL15474335 0.94 MEN1 (0.66) POLBMEN1KMT2AALDH1A1MAPT
SCHEMBL8060137 0.91 MEN1 (0.80) POLBMEN1KMT2AALDH1A1MAPT
SCHEMBL1924100 0.87 HTT (0.78) MEN1KMT2AALDH1A1MAPTGAA
SCHEMBL27486404 0.84 HTT (0.63) POLBMEN1KMT2AALDH1A1MAPT
SCHEMBL4592466 0.83 MAPT (0.69) POLBMEN1KMT2AALDH1A1MAPT
SCHEMBL9320377 0.83 HTT (0.67) MEN1KMT2AALDH1A1MAPTGAA
SCHEMBL2065031 0.82 CYP1A2 (0.69) MEN1KMT2AALDH1A1HTTCA1
SCHEMBL22628164 0.82 HTT (0.71) MEN1KMT2AALDH1A1L3MBTL1HTT
N-Benzylaniline SCHEMBL7840 0.82 HTT (0.71) MEN1KMT2AALDH1A1L3MBTL1HTT
SCHEMBL11935856 0.82 GAA (0.67) POLBMEN1KMT2AALDH1A1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1076649-A1 ISOQUINOLINE COMPOUND MELANOCORTIN RECEPTOR LIGANDS AND METHODS OF USING SAME TREGA BIOSCIENCES, INC. (US) 2001-02-21 EP claimed
WO-1999055679-A1 ISOQUINOLINE COMPOUND MELANOCORTIN RECEPTOR LIGANDS AND METHODS OF USING SAME TREGA BIOSCIENCES, INC. (US) 1999-11-04 WO claimed
EP-0064199-B1 NOVEL SECALONIC ACID DERIVATIVES AND METHOD FOR PREPARING THEREOF Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1985-08-21 EP claimed
CN-116102430-B Alkylation synthesis method for in-situ catalytic alcohols 中山大学 2025-03-14 CN disclosed
CN-110283130-B 1- (2, 5-dimethoxy phenyl) -3-substituted urea colon cancer inhibitor and preparation and application thereof 温州医科大学 2023-12-19 CN disclosed
US-11737461-B2 Citrate perhydrates and uses thereof BIOREM ENGINEERING SA (CH) 2023-08-29 US disclosed
US-20230210848-A1 CORONAVIRUS INFECTION THERAPEUTIC AGENT FORMED THROUGH COMBINATION OF PYRAZINE DERIVATIVE AND ANOTHER CORONAVIRUS INFECTION THERAPEUTIC DRUG FUJIFILM TOYAMA CHEMICAL CO., LTD. (JP) 2023-07-06 US disclosed
CN-116102430-A Alkylation synthesis method for in-situ catalytic alcohols 中山大学 2023-05-12 CN disclosed
US-20230137384-A1 ARTICLE OF MANUFACTURE COMPRISING LOCAL ANESTHETIC, BUFFER, AND GLYCOSAMINOGLYCAN IN SYRINGE WITH IMPROVED STABILITY URIGEN PHARMACEUTICALS, INC. 2023-05-04 US disclosed
CN-111807971-B Alkylation synthesis method for in-situ catalysis of alcohols 中山大学 2023-03-24 CN disclosed
EP-3998932-A1 ALKALIZATION OF URINARY BLADDER WALL PRIOR TO TREATMENT WITH INTRAVESICAL HEPARIN AND ALKALINIZED LIDOCAINE TO ENHANCE RELIEF OF BLADDER PAIN SYMPTOMS Parsons, C. Lowell (US) 2022-05-25 EP disclosed
EP-0114752-A2 Beta-lactam antibacterial agents BEECHAM GROUP PLC (GB) 1984-08-01 EP disclosed
EP-0114750-A2 Beta-lactam antibacterial agents BEECHAM GROUP PLC (GB) 1984-08-01 EP disclosed
EP-0112049-A1 Process for the preparation of beta-lactam compounds BEECHAM GROUP PLC (GB) 1984-06-27 EP disclosed
EP-0023045-B1 IMIDAZOLECARBOXYLIC ACID DERIVATIVES OF PENICILLINS AND CEPHALOSPORINS AJINOMOTO CO., INC. (JP) 1984-04-11 EP disclosed
EP-0080286-A1 Antibacterial compounds containing beta-lactams, processes for their preparation and their use BEECHAM GROUP PLC (GB) 1983-06-01 EP disclosed
EP-0068680-A1 Antibiotics BEECHAM GROUP PLC (GB) 1983-01-05 EP disclosed
EP-0026644-B1 ORTHO-TOLYL ESTER OF AN ALPHA-CARBOXY PENICILLIN, PROCESS FOR ITS PREPARATION AND PHARMACEUTICAL COMPOSITIONS COMPRISING THE PENICILLIN BEECHAM GROUP PLC (GB) 1982-12-01 EP disclosed
EP-0064199-A1 Novel secalonic acid derivatives and method for preparing thereof Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1982-11-10 EP disclosed
EP-0053539-A1 Cephalosporin derivatives, process for their preparation and pharmaceutical compositions containing them RHONE-POULENC SANTE (FR) 1982-06-09 EP 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 (3 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-20230210848-A1 CORONAVIRUS INFECTION THERAPEUTIC AGENT FORMED THROUGH COMBINATION OF PYRAZINE DERIVATIVE AND ANOTHER CORONAVIRUS INFECTION THERAPEUTIC DRUG ACE2, ACE, SARS1 POLB 4313/4885MEN1 4715/4885KMT2A 3813/4885
US-20230137384-A1 ARTICLE OF MANUFACTURE COMPRISING LOCAL ANESTHETIC, BUFFER, AND GLYCOSAMINOGLYCAN IN SYRINGE WITH IMPROVED STABILITY OGFR, ALOX5, PTGS1 POLB 2761/4885MEN1 4695/4885KMT2A 4584/4885
US-11737461-B2 Citrate perhydrates and uses thereof CS, HAGH, HOGA1 POLB 2280/4885MEN1 2931/4885KMT2A 2310/4885

“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.