SCHEMBL12296930

SCHEMBL12296930

CC(C)[Si](C#Cc1ccc2c3c(cccc13)C(=O)OC2=O)(C(C)C)C(C)C

nearest known ligand 0.45

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ TYMS P04818 5/20 0.45
▸ MEN1 O00255 2/20 0.35
▸ KMT2A Q03164 2/20 0.35
▸ POLB P06746 1/20 0.35
▸ KDM4E B2RXH2 2/20 0.34
▸ MAPT P10636 1/20 0.34
▸ PABPC1 P11940 1/20 0.34
▸ SMN1; SMN2 Q16637 1/20 0.34
▸ ALOX15 P16050 1/20 0.32
▸ TDP1 Q9NUW8 1/20 0.32
▸ KEAP1 Q14145 2/20 0.31
▸ NFE2L2 Q16236 2/20 0.31
▸ TLR9 Q9NR96 1/20 0.31
▸ USP2 O75604 1/20 0.31
▸ ATM Q13315 1/20 0.31
▸ ALDH1A1 P00352 1/20 0.31
▸ HPGD P15428 1/20 0.31

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
SCHEMBL12296929 0.83 KMT2A (0.49) MEN1KMT2APOLBKDM4EMAPT
SCHEMBL17172502 0.79 TYMS (0.53) TYMSMEN1KMT2APOLBKDM4E
SCHEMBL15705346 0.78 KMT2A (0.40) MEN1KMT2APOLBKDM4EMAPT
SCHEMBL12296926 0.75 KMT2A (0.40) MEN1KMT2APOLBKDM4EMAPT
SCHEMBL15843910 0.74 TYMS (0.50) TYMSMEN1KMT2APOLBKDM4E
SCHEMBL12405326 0.73 CACNA2D1 (0.35) —
SCHEMBL14918648 0.73 TYMS (0.47) TYMSMEN1KMT2APOLBKDM4E
SCHEMBL17172503 0.72 TYMS (0.41) TYMSMEN1KMT2APOLBALOX15
SCHEMBL18069179 0.71 TYMS (0.44) TYMSMEN1KMT2APOLBKDM4E
SCHEMBL31087627 0.70 TYMS (0.43) TYMSMEN1KMT2APOLBTDP1

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 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2334714-B1 METHOD OF PHOTOCHEMICAL HYDROLYSIS-POLYCONDENSATION OF CROSS-LINKABLE CHROMOPHORES WITH STERIC HINDRANCE, CATALYSED BY A PHOTOGENERATED ACID, AND THE APPLICATIONS THEREOF CENTRE NAT RECH SCIENT (FR) 2020-11-25 — — EP disclosed
US-8722318-B2 Methods of photochemical hydrolysis-polycondensation of cross-linkable chromophores with steric hindrance, catalysed by a photogenerated acid, and the applications thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE-CNRS (FR) 2014-05-13 — — US disclosed
US-8722318-B2 Methods of photochemical hydrolysis-polycondensation of cross-linkable chromophores with steric hindrance, catalysed by a photogenerated acid, and the applications thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE-CNRS (FR) 2014-05-13 — — US disclosed
US-20110229821-A1 Method of Photochemical Hydrolysis-Polycondensation of Cross-Linkable Chromophores with Steric Hindrance, Catalysed by a Photogenerated Acid, and the Applications Thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE-CNRS (FR) 2011-09-22 — — US disclosed
US-20110229821-A1 Method of Photochemical Hydrolysis-Polycondensation of Cross-Linkable Chromophores with Steric Hindrance, Catalysed by a Photogenerated Acid, and the Applications Thereof CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE-CNRS (FR) 2011-09-22 — — US disclosed
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