SCHEMBL8893904

SCHEMBL8893904

O=C(O)C[C@@H](O)C[C@@H](O)CCl

nearest known ligand 0.57

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
SLC22A6 Q4U2R8 1/20 0.57
GABRR1 P24046 2/20 0.48
LMNA P02545 1/20 0.48
MAPT P10636 1/20 0.43
SMN1; SMN2 Q16637 1/20 0.40
GPR84 Q9NQS5 4/20 0.39
TSHR P16473 1/20 0.36
CA1 P00915 2/20 0.36
CA2 P00918 2/20 0.36
CA9 Q16790 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
MMP2 P08253 1/20 0.32
MMP9 P14780 1/20 0.32
MMP12 P39900 1/20 0.32
MMP13 P45452 1/20 0.32
MMP14 P50281 1/20 0.32
HMGCR P04035 1/20 0.32

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
SCHEMBL3371887 1.00 SLC22A6 (0.57) SLC22A6GABRR1LMNAMAPTSMN1; SMN2
SCHEMBL2227091 1.00 SLC22A6 (0.57) SLC22A6GABRR1LMNAMAPTSMN1; SMN2
SCHEMBL17204173 1.00 SLC22A6 (0.57) SLC22A6GABRR1LMNAMAPTSMN1; SMN2
SCHEMBL1135965 1.00 SLC22A6 (0.57) SLC22A6GABRR1LMNAMAPTSMN1; SMN2
SCHEMBL30641549 1.00 SLC22A6 (0.57) SLC22A6GABRR1LMNAMAPTSMN1; SMN2
SCHEMBL30972500 0.87
SCHEMBL374298 0.87
SCHEMBL1405707 0.87
SCHEMBL2687087 0.87
SCHEMBL6453593 0.87 SLC22A6 (0.75) SLC22A6GABRR1LMNAMAPTSMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014203045-A1 A NOVEL, GREEN AND COST EFFECTIVE PROCESS FOR SYNTHESIS OF TERT-BUTYL (3R,5S)-6-OXO-3,5-DIHYDROXY-3,5-O-ISOPROPYLIDENE-HEXANOATE LUPIN LIMITED (IN) 2014-12-24 WO disclosed
US-5594153-A REACTING 6-HALO-3,5-DIHYDROXYHEXANOIC ACID OR DERIVATIVE THEREOF WITH DIETHER, KETONE OR UNSATURATED ETHER TO FORM 1,3-DIOXANE DERIVATIVE E. R. SQUIBB & SONS, INC. (US) 1997-01-14 US disclosed
US-5457227-A Condensing halo-substituted hydroxy ester with acetic acid, acetate salt or ester in presence of condensation agent to produce halo-substituted hydroxy keto ester E. R. SQUIBB & SONS, INC. (US) 1995-10-10 US disclosed
US-5278313-A Chemical condensation reaction E. R. SQUIBB & SONS, INC. (US) 1994-01-11 US disclosed