SCHEMBL5143956

SCHEMBL5143956

CC(=O)c1c(C)cc(NC(C)(C)C)nc1NC(C)(C)C

nearest known ligand 0.36

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
▸ SMN1; SMN2 Q16637 4/20 0.35
▸ CCNA2 P20248 1/20 0.33
▸ CDK2 P24941 1/20 0.33
▸ TTK P33981 1/20 0.33
▸ RPS27 P42677 1/20 0.33
▸ MAPK8 P45983 1/20 0.33
▸ MAPT P10636 1/20 0.33
▸ KDM4E B2RXH2 1/20 0.31
▸ GLP1R P43220 1/20 0.31
▸ ALDH1A1 P00352 1/20 0.31
▸ MAPK1 P28482 1/20 0.31
▸ LMNA P02545 2/20 0.31
▸ HPGD P15428 1/20 0.31
▸ PTBP1 P26599 1/20 0.31
▸ POLB P06746 2/20 0.30
▸ PIK3CG P48736 1/20 0.30
▸ HTT P42858 1/20 0.30

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
Bromide SCHEMBL11739645 0.98 SMN1; SMN2 (0.34) SMN1; SMN2CCNA2CDK2TTKRPS27
Hydrochloric Acid SCHEMBL11743005 0.98 SMN1; SMN2 (0.34) SMN1; SMN2CCNA2CDK2TTKRPS27
SCHEMBL11738008 0.94 GLP1R (0.37) SMN1; SMN2CCNA2CDK2TTKRPS27
SCHEMBL11733104 0.86 POLB (0.42) SMN1; SMN2CCNA2CDK2TTKRPS27
SCHEMBL11740878 0.84 CYP3A4 (0.41) CCNA2CDK2TTKRPS27MAPK8
SCHEMBL11744059 0.82 SLC29A1 (0.34) SMN1; SMN2CDK2KDM4EALDH1A1LMNA
SCHEMBL11738829 0.81 ALDH1A1 (0.40) CDK2MAPTALDH1A1HTT
SCHEMBL11737201 0.80 NPSR1 (0.33) SMN1; SMN2MAPK8KDM4EALDH1A1LMNA
SCHEMBL17393535 0.74 SMN1; SMN2 (0.57) SMN1; SMN2MAPTKDM4EALDH1A1MAPK1
SCHEMBL11716065 0.72 GLP1R (0.35) CDK2GLP1RLMNAPOLBHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5939568-A Accelerated catalysis of olefinic epoxidations THE SCRIPPS RESEARCH INSTITUTE (US) 1999-08-17 — — US claimed
US-20070072096-A1 Negative curable dye-containing composition, color filter, and method of manufacturing the same FUJI PHOTO FILM CO., LTD. 2007-03-29 — — US disclosed
EP-0483249-B1 METHOD OF TRANSCRIPTIONALLY MODULATING GENE EXPRESSION AND OF DISCOVERING CHEMICALS CAPABLE OF FUNCTIONING AS GENE EXPRESSION MODULATORS OSI PHARM INC (US) 2003-04-23 — — EP disclosed
US-5939568-A Accelerated catalysis of olefinic epoxidations THE SCRIPPS RESEARCH INSTITUTE (US) 1999-08-17 — — US disclosed
WO-1998033786-A9 ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS — 1998-12-30 — — WO disclosed
US-5665543-A Method of discovering chemicals capable of functioning as gene expression modulators ONCOGENE SCIENCE, INC. (US) 1997-09-09 — — US disclosed
EP-0483249-A4 — — 1994-04-06 — — EP disclosed
WO-1992012635-A1 METHODS OF TRANSCRIPTIONALLY MODULATING GENE EXPRESSION OF VIRAL GENES AND OTHER GENES ONCOGENE SCIENCE, INC. (US) 1992-08-06 — — WO disclosed
WO-1992013092-A1 METHODS OF TRANSCRIPTIONALLY MODULATING EXPRESSION OF HEMATOPOIETIC GROWTH FACTOR GENES ONCOGENE SCIENCE, INC. (US) 1992-08-06 — — WO disclosed
WO-1992013063-A1 METHODS OF TRANSCRIPTIONALLY MODULATING EXPRESSION OF GROWTH FACTOR GENES AND GROWTH FACTOR RECEPTOR GENES ONCOGENE SCIENCE, INC. (US) 1992-08-06 — — WO disclosed
EP-0483249-A1 METHOD OF TRANSCRIPTIONALLY MODULATING GENE EXPRESSION AND OF DISCOVERING CHEMICALS CAPABLE OF FUNCTIONING AS GENE EXPRESSION MODULATORS Oncogene Science, Inc. (US) 1992-05-06 — — EP disclosed
WO-1991001379-A1 METHOD OF TRANSCRIPTIONALLY MODULATING GENE EXPRESSION AND OF DISCOVERING CHEMICALS CAPABLE OF FUNCTIONING AS GENE EXPRESSION MODULATORS ONCOGENE SCIENCE, INC. (US) 1991-02-07 — — WO disclosed
US-4052510-A 4-ALKYL-2,6-DI(SECONDARY OR TERTIARY ALKYLAMINO) PYRIDINES, COMPOSITIONS THEREOF AND METHODS FOR TREATING DIABETES AND OBESITY SANDOZ, INC. (US) 1977-10-04 — — US disclosed
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