SCHEMBL7222392

SCHEMBL7222392

CCc1ccccc1SCC(=O)Cl

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HSD17B10 Q99714 3/20 0.42
▸ ACHE P22303 1/20 0.41
▸ CYP1A2 P05177 1/20 0.41
▸ POLB P06746 4/20 0.39
▸ RAB9A P51151 4/20 0.38
▸ GABRA1 P14867 1/20 0.38
▸ GABRB2 P47870 1/20 0.38
▸ L3MBTL1 Q9Y468 3/20 0.37
▸ LMNA P02545 2/20 0.37
▸ HTT P42858 1/20 0.37
▸ KMT2A Q03164 3/20 0.36
▸ ALDH1A1 P00352 2/20 0.36
▸ MEN1 O00255 2/20 0.36
▸ HPGD P15428 2/20 0.36
▸ MAPT P10636 1/20 0.36
▸ SMN1; SMN2 Q16637 1/20 0.36
▸ NPC1 O15118 2/20 0.36
▸ GAA P10253 2/20 0.36
▸ HSP90AA1 P07900 1/20 0.36
▸ BACE1 P56817 1/20 0.36

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
SCHEMBL21328440 0.83 CYP1A2 (0.59) HSD17B10ACHECYP1A2RAB9AKMT2A
SCHEMBL7223998 0.79 NOTUM (0.49) HSD17B10CYP1A2POLBRAB9AL3MBTL1
SCHEMBL21102240 0.79 HSD17B10 (0.41) HSD17B10ACHECYP1A2POLBRAB9A
SCHEMBL11864053 0.77 ALDH1A1 (0.51) HSD17B10CYP1A2POLBRAB9AL3MBTL1
SCHEMBL29297658 0.77 RAB9A (0.57) HSD17B10CYP1A2POLBRAB9AL3MBTL1
SCHEMBL14507031 0.76 GABRA1 (0.41) HSD17B10ACHEGABRA1GABRB2L3MBTL1
SCHEMBL30421739 0.76 HTR7 (0.44) HSD17B10CYP1A2POLBRAB9AL3MBTL1
SCHEMBL7417947 0.75 MTNR1A (0.55) HSD17B10POLBRAB9ALMNAHTT
SCHEMBL9661198 0.73 HSD17B10 (0.74) HSD17B10CYP1A2POLBRAB9AL3MBTL1
SCHEMBL16844673 0.72 PTGS2 (0.51) ACHEGABRA1GABRB2L3MBTL1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6552226-B1 Rapid; low temperature; one pot synthesis; reduced catalytic quantities of such as lewis acid and tertiary amine; entiomerically pure products THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2003-04-22 — — US disclosed
WO-2002026683-A1 TANDEM ACYL-CLAISEN REARRANGEMENT IN THE PREPARATION OF CHIRAL PRODUCTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2002-04-04 — — WO disclosed
US-6359174-B1 REACTING ALLYL REACTANT WITH ACID CHLORIDE IN PRESENCE OF LEWIS ACID CATALYST THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2002-03-19 — — US disclosed
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