SCHEMBL7186589

SCHEMBL7186589

CC(=O)OCC1(CO)CCCCC1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.34
ALDH1A1 P00352 3/20 0.34
HSD17B10 Q99714 2/20 0.34
CYP1A2 P05177 2/20 0.34
TSHR P16473 2/20 0.34
USP2 O75604 1/20 0.34
BLM P54132 1/20 0.34
CACNA2D1 P54289 1/20 0.34
SMN1; SMN2 Q16637 1/20 0.34
PRKCA P17252 9/20 0.32
JAK2 O60674 1/20 0.31
JAK1 P23458 1/20 0.31
TYK2 P29597 1/20 0.31
JAK3 P52333 1/20 0.31
APOBEC3A P31941 1/20 0.31
APOBEC3G Q9HC16 1/20 0.31
ABCB11 O95342 1/20 0.30
CHRM2 P08172 1/20 0.30
CHRM4 P08173 1/20 0.30
CYP3A4 P08684 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
SCHEMBL31196271 0.94 ALDH1A1 (0.36) LMNAALDH1A1HSD17B10PRKCA
SCHEMBL7195368 0.90 LMNA (0.39) LMNAALDH1A1HSD17B10CYP1A2TSHR
SCHEMBL30683844 0.87 ALDH1A1 (0.40) LMNAALDH1A1HSD17B10CYP1A2TSHR
SCHEMBL11376586 0.82 LMNA (0.33) LMNAALDH1A1HSD17B10CYP1A2TSHR
SCHEMBL1406401 0.82 MGAM (0.42) LMNAALDH1A1CYP1A2TSHRUSP2
SCHEMBL14482197 0.82 TSHR (0.39) LMNAALDH1A1CYP1A2TSHRUSP2
SCHEMBL159727 0.82 TSHR (0.39) LMNAALDH1A1CYP1A2TSHRUSP2
SCHEMBL5884497 0.82 TSHR (0.39) LMNAALDH1A1CYP1A2TSHRUSP2
SCHEMBL17272779 0.82 TSHR (0.39) LMNAALDH1A1CYP1A2TSHRUSP2
SCHEMBL10521389 0.82 TSHR (0.39) LMNAALDH1A1CYP1A2TSHRUSP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6600080-B1 Method of alcohols such as cyclohexanedimethanol, a benzyl ester is obtained, for example, by the reaction between a benzyl compound and carboxylic acid in the presence of oxygen and a catalyst including palladium, gold ultra fine particles NIPPON SHOKUBAI CO., LTD. (JP) 2003-07-29 US disclosed
EP-1090902-A2 Method for producing alcohols such as cyclohexanedimethanol Nippon Shokubai Co., Ltd. (JP) 2001-04-11 EP disclosed