SCHEMBL6915326

SCHEMBL6915326

O=CC(F)C(F)CSc1ccccc1

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAOA P21397 1/20 0.46
▸ MAOB P27338 1/20 0.46
▸ ALDH1A1 P00352 2/20 0.41
▸ MAPK1 P28482 1/20 0.41
▸ MTNR1A P48039 3/20 0.41
▸ MTNR1B P49286 3/20 0.41
▸ FFAR1 O14842 1/20 0.39
▸ NR3C1 P04150 1/20 0.35
▸ PGR P06401 1/20 0.35
▸ NR3C2 P08235 1/20 0.35
▸ DAO P14920 1/20 0.34
▸ MMP3 P08254 4/20 0.33
▸ MMP2 P08253 3/20 0.33
▸ MMP9 P14780 3/20 0.33
▸ KMT2A Q03164 2/20 0.33
▸ MMP13 P45452 2/20 0.33
▸ L3MBTL1 Q9Y468 1/20 0.33
▸ MMP1 P03956 1/20 0.33
▸ MMP8 P22894 1/20 0.33
▸ NPC1 O15118 1/20 0.33

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
SCHEMBL18560065 0.74 MAOA (0.56) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL6200206 0.74 MAOA (0.57) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL10403751 0.74 MAOA (0.47) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL10402449 0.74 MAOA (0.47) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL10402868 0.74 MAOA (0.57) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL7440144 0.71 MAOA (0.52) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL10404334 0.70 MTNR1A (0.50) MAOAMAOBALDH1A1MTNR1AMTNR1B
SCHEMBL10402862 0.68 CYP1A2 (0.44) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL2951869 0.68 MTNR1A (0.51) MAOAMAOBALDH1A1MAPK1MTNR1A
SCHEMBL26826115 0.68 MAOA (0.53) MAOAMAOBALDH1A1MAPK1MTNR1A

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-6818423-B2 LOW-MOLECULAR-WEIGHT C4-C6-KETONES DERIVATIZED WITH REMOVABLE GROUP ARE REACTED WITH CYANIDE GROUP DONOR IN PRESENCE OF HYDROXYNITRILE LYASE OR BY RACEMIC REACTION, ACIDIC HYDROLYSIS, OPTIONALLY RESOLUTION, AND CLEAVAGE OF THE GROUP DSM FINE CHEMICALS AUSTRIA NFG GMBH & CO KG (AU) 2004-11-16 — — US disclosed
US-20030092142-A1 Process for the preparation of chiral alpha-hydroxycarboxylic acids DSM FINE CHEMICALS AUSTRIA NFG GMBH & COKG (AT) 2003-05-15 — — US disclosed
Send feedback