SCHEMBL3768560

SCHEMBL3768560

O=c1oc2cc(O)ccc2c2c1CCCC2

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 6/20 1.00
ALDH1A1 P00352 6/20 1.00
HPGD P15428 5/20 1.00
HSD17B10 Q99714 5/20 1.00
TSHR P16473 4/20 1.00
GLA P06280 2/20 1.00
GAA P10253 2/20 1.00
CASP1 P29466 2/20 1.00
CASP7 P55210 2/20 1.00
CYP1A2 P05177 1/20 0.97
MAOA P21397 1/20 0.94
MAOB P27338 3/20 0.63
STS P08842 5/20 0.59
MEN1 O00255 1/20 0.59
KMT2A Q03164 1/20 0.59
PDE2A O00408 1/20 0.57
DRD2 P14416 1/20 0.56
DRD4 P21917 1/20 0.56
DRD3 P35462 1/20 0.56
MAPT P10636 3/20 0.56

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
SCHEMBL30465069 1.00 KDM4E (1.00) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL3625077 0.98 CYP1A2 (1.00) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL3762769 0.98 CYP1A2 (1.00) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL3757463 0.97 MAOA (1.00) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL10793789 0.87 ALDH1A1 (0.77) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL10791718 0.85 CYP1A2 (0.77) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL10795665 0.83 KDM4E (0.70) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL10790036 0.83 KDM4E (0.70) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL10789263 0.83 MAOA (0.77) KDM4EALDH1A1HPGDHSD17B10TSHR
SCHEMBL9336449 0.83 KDM4E (0.71) KDM4EALDH1A1HPGDHSD17B10TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11820751-B2 Urolithin derivatives and methods of use thereof VANDRIA SA (CH) 2023-11-21 US disclosed
CN-116178330-A Fluorescent probe, synthesis method and application 湖北大学 2023-05-30 CN disclosed
EP-2958906-A1 3-SUBSTITUTED-6H-BENZO[C]CHROMEN-6-ONES AND 3-SUBSTITUTED-7,8,9,10-TETRAHYDRO-6H-BENZO[C]CHROMEN-6-ONES AGAINST SENILE DEMENTIA Nobel Ilaç Sanayii Ve Ticaret A.S. (TR) 2015-12-30 EP disclosed
WO-2014129989-A1 3-SUBSTITUTED-6H-BENZO[C]CHROMEN-6-ONES AND 3-SUBSTITUTED-7,8,9,10-TETRAHYDRO-6H-BENZO[C]CHROMEN-6-ONES AGAINST SENILE DEMENTIA FARGEM FARMASÖTİK ARAŞTIRMA GELİŞTİRME MERKEZİ SANAYİ VE TİCARET A.Ş. (TR) 2014-08-28 WO disclosed
WO-2014129989-A1 3-SUBSTITUTED-6H-BENZO[C]CHROMEN-6-ONES AND 3-SUBSTITUTED-7,8,9,10-TETRAHYDRO-6H-BENZO[C]CHROMEN-6-ONES AGAINST SENILE DEMENTIA FARGEM FARMASÖTİK ARAŞTIRMA GELİŞTİRME MERKEZİ SANAYİ VE TİCARET A.Ş. (TR) 2014-08-28 WO disclosed
US-7846965-B2 a non-steroidal sulphamate compound such as 6-Oxo-8,9,10,11-tetrahydro-7H-cyclohepta-[c][1]benzopyran-3-O-sulphamate, suitable for use as an inhibitor of estrone sulphatase, for the treatment of endocrine-dependent cancers and tumors, such as the breast and endometrium STERIX LIMITED (GB) 2010-12-07 US disclosed
EP-1957475-A1 CHROMENONES AND THEIR USE AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS Merz Pharma GmbH & Co.KGaA (DE) 2008-08-20 EP disclosed
US-20070173531-A1 Compound REED MICHAEL J 2007-07-26 US disclosed
WO-2007045876-A1 CHROMENONES AND THEIR USE AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS MERZ PHARMA GMBH & CO. KGAA (DE) 2007-04-26 WO disclosed
WO-2007045876-A1 CHROMENONES AND THEIR USE AS MODULATORS OF METABOTROPIC GLUTAMATE RECEPTORS MERZ PHARMA GMBH & CO. KGAA (DE) 2007-04-26 WO disclosed
US-4681954-A 7,8,9,10-tetrahydro-6-oxo-6H-dibenzo(b,d)pyranyloxy-propanes PENNWALT CORPORATION (US) 1987-07-21 US disclosed
EP-0221293-A1 7,8,9,10-Tetrahydro-6-oxo-6H-dibenzo[b,d]pyranyloxy-propanes PENNWALT CORPORATION (US) 1987-05-13 EP disclosed
EP-0218195-A2 Bis(dibenzo[b,d]pyranyloxy)propanes PENNWALT CORPORATION (US) 1987-04-15 EP disclosed
US-4647674-A Bis-(dibenzo[b,d]pyranyloxy) propanes PENNWALT CORPORATION (US) 1987-03-03 US disclosed
US-4618622-A ANTIDEPRESSANTS, ANTIALLERGENS BASF AKTIENGESELLSCHAFT (DE) 1986-10-21 US disclosed
US-4569994-A Dibenzo[b,d]pyranyloxyaminopropanols PENNWALT CORPORATION 1986-02-11 US disclosed
EP-0043535-B1 TRICYCLIC ARYLIC ETHERS, PROCESS FOR THEIR PREPARATION AND MEDICINES CONTAINING THESE COMPOUNDS Roche Diagnostics GmbH (DE) 1984-10-31 EP disclosed
EP-0111746-A2 Sulfonic-acid esters of hydroxycoumarines, their preparation and medicines containing them BASF Aktiengesellschaft (DE) 1984-06-27 EP disclosed
US-4382943-A DIHYDROCYCLOPENTA/C//1/BENZOPYRAN-4-/1H/ONES BOEHRINGER MANNHEIM GMBH (DE) 1983-05-10 US disclosed
EP-0043535-A1 Tricyclic arylic ethers, process for their preparation and medicines containing these compounds Roche Diagnostics GmbH (DE) 1982-01-13 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 (2 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-20070173531-A1 Compound HSD17B11, NR5A1, CYP17A1 KDM4E 1129/4885ALDH1A1 611/4885HPGD 260/4885
US-11820751-B2 Urolithin derivatives and methods of use thereof NLN, UQCRC2, TUFM KDM4E 4333/4885ALDH1A1 851/4885HPGD 499/4885

“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.