SCHEMBL2929675

SCHEMBL2929675

O=C1CC(O)c2ccccc21

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AR P10275 4/20 0.46
ADORA3 P0DMS8 3/20 0.46
HSD11B1 P28845 1/20 0.46
AKR1C3 P42330 1/20 0.46
S100A4 P26447 1/20 0.45
EDNRB P24530 1/20 0.42
EDNRA P25101 1/20 0.42
PARP3 Q9Y6F1 1/20 0.42
KDM4E B2RXH2 1/20 0.40
CYP19A1 P11511 1/20 0.40
MAOB P27338 1/20 0.40
HSD17B10 Q99714 1/20 0.40
ALDH1A1 P00352 1/20 0.39
AXL P30530 1/20 0.39
CYP3A4 P08684 2/20 0.39
NPC1 O15118 1/20 0.39
MAPT P10636 1/20 0.39
MAPK1 P28482 1/20 0.39
RAB9A P51151 1/20 0.39
GLS O94925 1/20 0.38

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
SCHEMBL30737888 1.00 AR (0.46) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL19302757 1.00 AR (0.46) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL11869980 1.00 AR (0.46) ARADORA3HSD11B1AKR1C3S100A4
(-)-4-Hydroxy-Alpha-Tetralone SCHEMBL3694170 0.81 POLL (0.50) ARADORA3HSD11B1AKR1C3S100A4
(-)-4-Hydroxy-Alpha-Tetralone SCHEMBL14592023 0.81 POLL (0.50) ARADORA3HSD11B1AKR1C3S100A4
(-)-4-Hydroxy-Alpha-Tetralone SCHEMBL19420220 0.81 POLL (0.50) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL8673469 0.80 S100A4 (0.59) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL12405330 0.79 S100A4 (0.47) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL19774841 0.78 MEN1 (0.39) ARADORA3HSD11B1AKR1C3S100A4
SCHEMBL14166580 0.78 CYP2A6 (0.46) ARADORA3HSD11B1AKR1C3S100A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240190926-A1 P450-BM3 VARIANTS WITH IMPROVED ACTIVITY CODEXIS, INC. 2024-06-13 US claimed
CN-113072435-B Preparation method of 3-hydroxy-1-indanone derivative containing alkenyl fluorine 浙江工业大学 2022-04-29 CN claimed
CN-113072435-A Preparation method of 3-hydroxy-1-indanone derivative containing alkenyl fluorine 浙江工业大学 2021-07-06 CN claimed
US-12577526-B2 Massively parallel on-chip construction of synthetic microbial communities THE BROAD INSTITUTE, INC. (US) 2026-03-17 US disclosed
US-20250376656-A1 MASSIVELY PARALLEL ON-CHIP CONSTRUCTION OF SYNTHETIC MICROBIAL COMMUNITIES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2025-12-11 US disclosed
US-20250215464-A1 ENGINEERED ENZYME FOR PREPARING A HYDROXYLATED INDANONE INTERMEDIATE USEFUL IN THE SYNTHESIS OF BELZUTIFAN MERCK SHARP & DOHME LLC (US) 2025-07-03 US disclosed
CN-119546622-A Engineering enzymes for preparing hydroxylated indanone intermediates useful for synthesis of bezotevans 默沙东有限责任公司 2025-02-28 CN disclosed
US-20240190926-A1 P450-BM3 VARIANTS WITH IMPROVED ACTIVITY CODEXIS, INC. 2024-06-13 US disclosed
WO-2024112781-A1 P450-BM3 VARIANTS WITH IMPROVED ACTIVITY CODEXIS, INC. (US) 2024-05-30 WO disclosed
WO-2024042217-A1 METHODS OF MODIFYING METHYLCYTOSINE OR DERIVATIVE THEREOF USING A NUCLEOPHILIC MOLECULE, AND METHODS OF USING THE SAME TO DETECT THE METHYLCYTOSINE OR DERIVATIVE THEREOF IN A POLYNUCLEOTIDE ILLUMINA, INC. (US) 2024-02-29 WO disclosed
WO-2024010783-A1 ENGINEERED ENZYME FOR PREPARING A HYDROXYLATED INDANONE INTERMEDIATE USEFUL IN THE SYNTHESIS OF BELZUTIFAN MERCK SHARP & DOHME LLC (US) 2024-01-11 WO disclosed
EP-2570418-A2 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles compound OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2013-03-20 EP disclosed
EP-1555267-B1 2,3-DIHYDRO-6-NITROIMIDAZO[2,1-b]OXAZOLES OTSUKA PHARMA CO LTD (JP) 2013-01-16 EP disclosed
US-20120231972-A1 Probe Compound for Detecting and Isolating Enzymes and Means and Methods Using the Same INSTITUTE OF CATALYSIS (CSIC) (ES) 2012-09-13 US disclosed
EP-2230312-A1 Probe compound for detecting and isolating enzymes and means and methods using the same Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2010-09-22 EP disclosed
US-7262212-B2 2,3-dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2007-08-28 US disclosed
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-05-04 US disclosed
EP-1555267-A1 2,3-DIHYDRO-6-NITROIMIDAZO 2,1-b OXAZOLES OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-07-20 EP disclosed
US-4078934-A Photosensitive, image-forming composition containing a leuco 2,3-disubstituted-1-indanone and a photooxidant E. I. DU PONT DE NEMOURS AND COMPANY (US) 1978-03-14 US disclosed
US-3992450-A PHOTOSENSITIVE COMPOSITIONS E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-11-16 US 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-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles NR2C2, NR4A3, NR4A2 AR 254/4885ADORA3 203/4885HSD11B1 256/4885
US-20120231972-A1 Probe Compound for Detecting and Isolating Enzymes and Means and Methods Using the Same SI, GUSB, MPI AR 3427/4885ADORA3 2034/4885HSD11B1 508/4885
US-20240190926-A1 P450-BM3 VARIANTS WITH IMPROVED ACTIVITY CYP3A43, CYP4F3, CYP1A2 AR 636/4885ADORA3 865/4885HSD11B1 84/4885
US-12577526-B2 Massively parallel on-chip construction of synthetic microbial communities STUB1, SAMM50, CD14 AR 4066/4885ADORA3 3764/4885HSD11B1 2124/4885

“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.