SCHEMBL1836933

SCHEMBL1836933

CC1(C)CC(NC(=O)Oc2ccc(Cl)cc2)CC(C)(CNC(=O)Oc2ccc(Cl)cc2)C1

nearest known ligand 0.60

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.60
TAAR1 Q96RJ0 1/20 0.40
TRPV1 Q8NER1 1/20 0.39
FAAH O00519 3/20 0.38
LIPE Q05469 3/20 0.38
ATF4 P18848 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
ALDH1A1 P00352 1/20 0.35
RAB9A P51151 1/20 0.35

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
SCHEMBL18092130 0.93 TSHR (0.55) TSHRTAAR1TRPV1FAAHLIPE
SCHEMBL983463 0.88 TSHR (0.63) TSHRFAAHALDH1A1RAB9A
SCHEMBL1840943 0.87 TSHR (0.58) TSHRFAAHALDH1A1RAB9A
SCHEMBL16942584 0.87 TSHR (0.58) TSHRALDH1A1RAB9A
Carbamic Acid SCHEMBL29886440 0.85 TSHR (0.59) TSHRFAAHALDH1A1RAB9A
SCHEMBL19491097 0.84 TSHR (0.71) TSHRTAAR1FAAHTDP1ALDH1A1
SCHEMBL1952531 0.84 TSHR (0.55) TSHRTRPV1TDP1RAB9A
SCHEMBL1952647 0.84 TSHR (0.55) TSHRTDP1ALDH1A1RAB9A
SCHEMBL18419017 0.84 TSHR (0.57) TSHRTDP1ALDH1A1RAB9A
SCHEMBL16141999 0.83 TSHR (0.54) TSHRFAAHTDP1ALDH1A1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2322504-A1 PROCESS FOR THE PREPARATION OF N-SUBSTITUTED CARBAMIC ACID ESTER AND PROCESS FOR THE PREPARATION OF ISOCYANATE USING THE N-SUBSTITUTED CARBAMIC ACID ESTER Asahi Kasei Chemicals Corporation (JP) 2011-05-18 EP disclosed