SCHEMBL6237632

SCHEMBL6237632

CCCCCc1cc(C)cc(=O)o1

nearest known ligand 0.82

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.82
SMN1; SMN2 Q16637 4/20 0.82
CA1 P00915 1/20 0.45
CA9 Q16790 1/20 0.45
ALDH1A1 P00352 4/20 0.44
HTT P42858 3/20 0.44
ALOX15 P16050 1/20 0.44
ELANE P08246 3/20 0.43
TP53 P04637 1/20 0.43
GAA P10253 1/20 0.43
TSHR P16473 1/20 0.43
SIRT2 Q8IXJ6 1/20 0.42
HCAR2 Q8TDS4 2/20 0.41
KDM4E B2RXH2 2/20 0.39
KMT2A Q03164 1/20 0.39
HSD17B10 Q99714 1/20 0.37
STS P08842 1/20 0.37
SRC P12931 1/20 0.37

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
SCHEMBL27909290 0.98 MAPT (0.86) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL11854128 0.98 MAPT (0.86) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL11859633 0.98 MAPT (0.86) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL11858889 0.98 MAPT (0.86) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL11779539 0.94 MAPT (0.79) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL30165066 0.90 MAPT (1.00) MAPTSMN1; SMN2CA1CA9ALDH1A1
SCHEMBL2782253 0.80 MAPT (0.53) MAPTSMN1; SMN2ALDH1A1HTTALOX15
SCHEMBL563659 0.80 ALOX15 (0.54) MAPTSMN1; SMN2ALDH1A1HTTALOX15
SCHEMBL11847254 0.80 MAPT (0.72) MAPTSMN1; SMN2CA1CA9HCAR2
SCHEMBL6905774 0.79 MAPT (0.56) MAPTSMN1; SMN2ALDH1A1HTTALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1024695-B1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2005-06-22 EP claimed
EP-1024695-A4 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2002-04-03 EP claimed
US-6251832-B1 MIXTURE OF FUNGICIDE AND ONE OR MORE CARRIERS, ADJUVANTS AND/OR DILUENTS; FOR AGRICULTURAL OR HORTICULTURAL USE CUTLER, HORACE G. 2001-06-26 US claimed
EP-1024695-A1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE Cutler, Horace G. (US) 2000-08-09 EP claimed
WO-1999004633-A1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE THE HORTICULTURE AND FOOD RESEARCH INSTITUTE OF NEW ZEALAND LIMITED (NZ) 1999-02-04 WO claimed
US-11753379-B2 Process for forming 2-hydroxypyridine-1-oxide or derivatives thereof CLARIANT INTERNATIONAL LTD (CH) 2023-09-12 US disclosed
CN-110372654-B Method for synthesizing 4-methyl-6- (2, 4-trimethyl amyl) -2H-pyran-2-ketone by two-step method 成武县晨晖环保科技有限公司 2023-05-23 CN disclosed
EP-1024695-B1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2005-06-22 EP disclosed
EP-1024695-B1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2005-06-22 EP disclosed
EP-1024695-A4 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2002-04-03 EP disclosed
EP-1024695-A4 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE CUTLER HORACE G (US) 2002-04-03 EP disclosed
WO-2001051481-A1 METHOD FOR THE SYNTHESIS OF 6N-PENTYL-2H-PYRAN-2-ONE CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2001-07-19 WO disclosed
EP-1024695-A1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE Cutler, Horace G. (US) 2000-08-09 EP disclosed
WO-1999004633-A1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE THE HORTICULTURE AND FOOD RESEARCH INSTITUTE OF NEW ZEALAND LIMITED (NZ) 1999-02-04 WO disclosed
WO-1999004633-A1 FUNGICIDE COMPRISING 4-METHYL-6-PENTYL-2H-PYRAN-2-ONE THE HORTICULTURE AND FOOD RESEARCH INSTITUTE OF NEW ZEALAND LIMITED (NZ) 1999-02-04 WO disclosed
US-5137035-A With combustible filler of natural tobacco, reconstituted tobacco or tobacco substitutes PHILIP MORRIS INCORPORATED (US) 1992-08-11 US disclosed
US-5120368-A VANILLIN 5-HYDROXYESTERS AND SMOKING COMPOSITIONS CONTAINING A VANILLIN-RELEASE ADDITIVE PHILIP MORRIS INCORPORATED (US) 1992-06-09 US disclosed
US-5114493-A Smoking compositions containing a hexahydrobenzofuranone flavorant PHILIP MORRIS INC. (US) 1992-05-19 US disclosed
EP-0470766-A2 Smoking composition containing a vanillin-release additive Philip Morris Products Inc. (US) 1992-02-12 EP disclosed
US-4690157-A DERIVATIVES OF BUTYROLACTONE OR VALEROLACTONE; CIGARETTES PHILIP MORRIS INCORPORATED (US) 1987-09-01 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 (1 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-11753379-B2 Process for forming 2-hydroxypyridine-1-oxide or derivatives thereof HMOX2, HMOX1, HPD MAPT 4348/4885SMN1; SMN2 1390/4885CA1 1693/4885

“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.