SCHEMBL27520109

SCHEMBL27520109

CCC(=O)c1ccc(O)cc1Cl

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HSP90AB1 P08238 1/20 0.67
MAPT P10636 3/20 0.50
RAB9A P51151 2/20 0.50
NPC1 O15118 1/20 0.50
CASP3 P42574 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
SENP8 Q96LD8 1/20 0.50
SENP7 Q9BQF6 1/20 0.50
SENP6 Q9GZR1 1/20 0.50
ALDH1A1 P00352 2/20 0.47
MAPK1 P28482 1/20 0.47
HIF1A Q16665 1/20 0.47
HSD17B10 Q99714 1/20 0.45
HTT P42858 1/20 0.45
POLB P06746 1/20 0.44
ESRRB O95718 1/20 0.43
ESRRG P62508 1/20 0.43
CA12 O43570 1/20 0.43
CA1 P00915 1/20 0.43
CA2 P00918 1/20 0.43

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
SCHEMBL11195785 0.85 HTT (0.54) HSP90AB1MAPTRAB9ANPC1CASP3
SCHEMBL10990106 0.85 HSP90AB1 (0.61) HSP90AB1MAPTRAB9ANPC1CASP3
SCHEMBL1144066 0.82 ALDH1A1 (0.69) HSP90AB1MAPTRAB9ANPC1SMN1; SMN2
SCHEMBL16432142 0.82 ALDH1A1 (0.69) HSP90AB1MAPTRAB9ANPC1CASP3
SCHEMBL29712843 0.82 ALDH1A1 (0.69) HSP90AB1MAPTRAB9ANPC1SMN1; SMN2
SCHEMBL6579360 0.81 PTPN1 (0.48) HSP90AB1MAPTRAB9ANPC1CASP3
SCHEMBL481085 0.80 HSP90AB1 (1.00) HSP90AB1MAPTRAB9ANPC1SMN1; SMN2
SCHEMBL4706474 0.80 HSP90AB1 (1.00) HSP90AB1MAPTRAB9ANPC1SMN1; SMN2
SCHEMBL29457585 0.80 HSP90AB1 (1.00) HSP90AB1MAPTRAB9ANPC1SMN1; SMN2
SCHEMBL10031578 0.79 CHRM2 (0.52) HSP90AB1MAPTALDH1A1MAPK1HIF1A

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
CN-1228448-C Process for preparing chiral medicine intermediate (R)-2-halogen-1-(substituted phenyl) ethanol TIANJIN NANKAI GUARD CO LTD (CN) 2005-11-23 CN disclosed
CN-1554767-A Process for preparing chiral medicine intermediate (R)-2-halogen-1-(substituted phenyl) ethanol 天津南开戈德集团有限公司 2004-12-15 CN disclosed