SCHEMBL4960851

SCHEMBL4960851

c1cnc2cc3c(cc2c1)C1CNCC3C1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
▸ CHRNB2 P17787 6/20 0.67
▸ CHRNA4 P43681 6/20 0.67
▸ CHRNB4 P30926 3/20 0.67
▸ CHRNA3 P32297 3/20 0.67
▸ CHRNA1 P02708 1/20 0.67
▸ ESR1 P03372 1/20 0.67
▸ CHRNG P07510 1/20 0.67
▸ CHRNB1 P11230 1/20 0.67
▸ CHRNA5 P30532 1/20 0.67
▸ CHRNA7 P36544 1/20 0.67
▸ HTR3A P46098 1/20 0.67
▸ CHRND Q07001 1/20 0.67
▸ CHRNA2 Q15822 1/20 0.67

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
SCHEMBL10025840 0.82 CHRNB4 (0.42) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL225687 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL14003841 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL137144 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL5959022 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL29710884 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL29363551 0.81 CHRNB2 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL31413921 0.79 CHRNB4 (1.00) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
Varenicline SCHEMBL20553851 0.79 CHRNB2 (0.96) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1
SCHEMBL11932910 0.79 CHRNB4 (0.68) CHRNB2CHRNA4CHRNB4CHRNA3CHRNA1

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-1383733-B1 PROCESS FOR THE PREPARATION OF 1,3-SUBSTITUTED INDENES AND ARYL-FUSED AZAPOLYCYCLIC COMPOUNDS PFIZER PROD INC (US) 2008-03-05 — — EP disclosed
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