SCHEMBL199386

SCHEMBL199386

CCc1cc(C(C)(C)C)cc(CC)c1O

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 6/20 0.61
GABRA1 P14867 2/20 0.52
GABRB2 P47870 2/20 0.52
CYP2C9 P11712 6/20 0.47
CYP2D6 P10635 5/20 0.47
CYP1A2 P05177 5/20 0.47
HIF1A Q16665 2/20 0.47
ESR1 P03372 3/20 0.45
ESR2 Q92731 3/20 0.45
ALOX15 P16050 2/20 0.45
MAPK1 P28482 1/20 0.45
HTT P42858 1/20 0.45
HSPA5 P11021 1/20 0.42
CYP3A4 P08684 2/20 0.40
TSHR P16473 3/20 0.40
SMN1; SMN2 Q16637 1/20 0.39
NR5A2 O00482 1/20 0.39
NR5A1 Q13285 1/20 0.39
HSD17B10 Q99714 2/20 0.38
ALDH1A1 P00352 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
SCHEMBL16081366 0.90 CYP2C19 (0.52) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL31603748 0.89 CYP2C19 (0.51) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL10046766 0.89 CYP2C19 (0.51) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL14997935 0.88 CYP2C19 (0.50) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL29404283 0.87 HSPA5 (0.55) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL8028498 0.87 HSPA5 (0.55) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL10046743 0.87 CYP2C19 (0.49) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL14665356 0.87 CYP2C19 (0.49) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL13609095 0.86 GABRA1 (0.52) CYP2C19GABRA1GABRB2CYP2C9CYP2D6
SCHEMBL948481 0.86 ALOX15 (0.61) CYP2C19GABRA1GABRB2CYP2C9CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4013379-B1 NO STAINING ANTIPERSPIRANT COMPOSITION UNILEVER IP HOLDINGS B V (NL) 2025-01-08 EP claimed
CN-113383273-B Photosensitive resin composition, pattern forming method, cured film, laminate, and device 富士胶片株式会社 2023-11-14 CN disclosed
CN-110692018-B Photosensitive resin composition, polymer precursor, cured film, laminate, method for producing cured film, and semiconductor device 富士胶片株式会社 2023-11-03 CN disclosed
US-20230280648-A1 COMPOSITION FOR FORMING METAL OXIDE FILM, PATTERNING PROCESS, AND METHOD FOR FORMING METAL OXIDE FILM SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-09-07 US disclosed
US-20230244147-A1 COMPOSITION FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND COMPOUND AND POLYMER FOR FORMING ORGANIC FILM SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-08-03 US disclosed
CN-110741318-B Photosensitive resin composition, cured film, laminate, method for producing cured film, and semiconductor device 富士胶片株式会社 2023-06-30 CN disclosed
US-20230161251-A1 COMPOSITION FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND COMPOUND AND POLYMER FOR FORMING ORGANIC FILM SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-05-25 US disclosed
US-20230161251-A1 COMPOSITION FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND COMPOUND AND POLYMER FOR FORMING ORGANIC FILM SHIN-ETSU CHEMICAL CO., LTD. (JP) 2023-05-25 US disclosed
CN-109417058-B Method for manufacturing wafer and laminate 富士胶片株式会社 2023-04-18 CN disclosed
CN-112888714-B Method for producing cured film, resin composition, cured film, method for producing laminate, and method for producing semiconductor element 富士胶片株式会社 2023-02-28 CN disclosed
US-8071775-B2 photovoltaics; emitters in chemiluminescence applications; field-effect transistors and electrophotography; N,N'-Bis(2,6-diisopropylphenyl)-1,7- and -1,6-bis(2,6-diisopropylphenoxy)-perylene-3,4:9,10-tetracarboximide BASF AKTIENGESELLSCHAFT (DE) 2011-12-06 US disclosed
US-20110165691-A1 AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS BASF SE (DE) 2011-07-07 US disclosed
EP-2307507-A2 NEW AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS BASF SE (DE) 2011-04-13 EP disclosed
US-20100207072-A1 USE OF RYLENE DERIVATIVES AS ACTIVE COMPONENTS IN SOLAR CELLS AND PHOTODETECTORS BASF SE (DE) 2010-08-19 US disclosed
US-20100048904-A1 DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS BASF AKTIENGESELLSCHAFT (DE) 2010-02-25 US disclosed
WO-2010010198-A2 NEW AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS BASF SE (DE) 2010-01-28 WO disclosed
US-20100022021-A1 NEW AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS BASF SE (DE) 2010-01-28 US disclosed
US-20080287678-A1 Multiple Chromophores Based on Rylene BASF AKTIENGESELLSCHAFT (DE) 2008-11-20 US disclosed
US-20080245411-A1 Fluorescent Solar Conversion Cells Based on Fluorescent Terylene Dyes BASF SE 2008-10-09 US disclosed
US-20080167467-A1 Substituted Rylene Derivatives BASF AKTIENGESELLSCHAFT (DE) 2008-07-10 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 (8 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-20080167467-A1 Substituted Rylene Derivatives NR3C2, NR2C2, NR2E3 CYP2C19 433/4885GABRA1 994/4885GABRB2 594/4885
US-20100048904-A1 DIBENZORYLENETETRACARBOXIMIDES AS INFRARED ABSORBERS TDO2, C9, CYP3A43 CYP2C19 42/4885GABRA1 1449/4885GABRB2 870/4885
US-20230161251-A1 COMPOSITION FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND COMPOUND AND POLYMER FOR FORMING ORGANIC FILM PYM1, OR10J3, C5 CYP2C19 2677/4885GABRA1 3291/4885GABRB2 3524/4885
US-20100022021-A1 NEW AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS NANS, NANP, GNE CYP2C19 635/4885GABRA1 3250/4885GABRB2 3809/4885
US-20110165691-A1 AZIDE SUBSTITUTED NAPHTHYLENE OR RYLENE IMIDE DERIVATIVES AND THEIR USE AS REAGENTS IN CLICK-REACTIONS NANS, NANP, GNE CYP2C19 456/4885GABRA1 3121/4885GABRB2 3726/4885
US-20100207072-A1 USE OF RYLENE DERIVATIVES AS ACTIVE COMPONENTS IN SOLAR CELLS AND PHOTODETECTORS NR2E3, NR1H2, NR1H3 CYP2C19 1088/4885GABRA1 2610/4885GABRB2 1884/4885
US-20080287678-A1 Multiple Chromophores Based on Rylene TDO2, PPOX, NPY1R CYP2C19 34/4885GABRA1 2209/4885GABRB2 2196/4885
US-20230244147-A1 COMPOSITION FOR FORMING ORGANIC FILM, PATTERNING PROCESS, AND COMPOUND AND POLYMER FOR FORMING ORGANIC FILM OR10J3, PYM1, AP1M1 CYP2C19 2076/4885GABRA1 2701/4885GABRB2 3464/4885

“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.