SCHEMBL27459568

SCHEMBL27459568

O=CC(=O)c1c[nH]c2cc(-c3ccccc3)ccc12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PRKAB2 O43741 4/20 0.50
▸ PRKAG1 P54619 4/20 0.50
▸ PRKAA2 P54646 4/20 0.50
▸ PRKAA1 Q13131 4/20 0.50
▸ PRKAG3 Q9UGI9 4/20 0.50
▸ PRKAG2 Q9UGJ0 4/20 0.50
▸ PRKAB1 Q9Y478 4/20 0.50
▸ NR4A2 P43354 1/20 0.50
▸ NPC1 O15118 1/20 0.47
▸ RAB9A P51151 1/20 0.47
▸ TDP1 Q9NUW8 1/20 0.47
▸ IMPDH2 P12268 1/20 0.47
▸ DGAT1 O75907 1/20 0.46
▸ GPR84 Q9NQS5 1/20 0.42
▸ SCN9A Q15858 1/20 0.41
▸ TUBB4A P04350 1/20 0.41
▸ TUBB P07437 1/20 0.41
▸ TUBA3C P0DPH7 1/20 0.41
▸ TUBA1B P68363 1/20 0.41
▸ TUBA4A P68366 1/20 0.41

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
SCHEMBL2728702 0.79 GPR84 (0.67) NR4A2NPC1RAB9ATDP1IMPDH2
Hydrochloric Acid SCHEMBL26136311 0.78 GPR84 (0.65) NR4A2NPC1RAB9ATDP1IMPDH2
SCHEMBL10835850 0.78 ALDH1A1 (0.59) PRKAB2PRKAG1PRKAA2PRKAA1PRKAG3
SCHEMBL27452734 0.77 NR4A2 (0.41) NR4A2NPC1RAB9ATDP1GPR84
SCHEMBL28770407 0.77 NR4A2 (0.61) NR4A2GPR84TUBB1ALDH1A1
SCHEMBL27728105 0.77 CYP2A6 (0.57) NR4A2NPC1RAB9ATDP1IMPDH2
SCHEMBL27984527 0.77 NR4A2 (0.63) PRKAB2PRKAG1PRKAA2PRKAA1PRKAG3
SCHEMBL2535062 0.75 CYP2A6 (0.61) NR4A2IMPDH2ALDH1A1TNKS2
SCHEMBL7846022 0.74 KDM4E (0.55) PRKAB2PRKAG1PRKAA2PRKAA1PRKAG3
SCHEMBL28745891 0.73 GABRA1 (0.48) NR4A2

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
CN-1144800-A 3-ketoindole derivates taken as potassium channels regulator BRISTOL MYERS SQUIBB CO (US) 1997-03-12 — — CN disclosed
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