SCHEMBL9915610

SCHEMBL9915610

CB(O)N1CCN(c2ccccc2)CC1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CHRNA7 P36544 2/20 0.50
▸ SIGMAR1 Q99720 2/20 0.47
▸ DRD2 P14416 1/20 0.47
▸ ALOX15 P16050 2/20 0.47
▸ CYP3A4 P08684 1/20 0.47
▸ CHRNB2 P17787 1/20 0.47
▸ NFKB1 P19838 1/20 0.47
▸ MAPK1 P28482 1/20 0.47
▸ CHRNA3 P32297 1/20 0.47
▸ CHRNA4 P43681 1/20 0.47
▸ HSD17B10 Q99714 1/20 0.47
▸ USP2 O75604 2/20 0.46
▸ TSHR P16473 2/20 0.46
▸ SMN1; SMN2 Q16637 2/20 0.46
▸ MAPT P10636 4/20 0.46
▸ MEN1 O00255 3/20 0.46
▸ KMT2A Q03164 3/20 0.46
▸ ALDH1A1 P00352 1/20 0.46
▸ PHGDH O43175 1/20 0.46
▸ MGLL Q99685 1/20 0.46

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
SCHEMBL9915611 0.81 AKR1C3 (0.46) DRD2USP2MAPTKMT2AALDH1A1
SCHEMBL12556830 0.81 MAPT (0.58) ALOX15MAPK1HSD17B10USP2SMN1; SMN2
SCHEMBL14617528 0.80 ADRA2C (0.62) DRD2ALOX15MAPK1SMN1; SMN2MAPT
SCHEMBL9915612 0.78 CHKA (0.57) DRD2ALOX15USP2TSHRSMN1; SMN2
SCHEMBL164538 0.78 LMNA (0.67) CHRNA7SIGMAR1DRD2ALOX15CYP3A4
SCHEMBL576814 0.78 LMNA (0.67) CHRNA7SIGMAR1DRD2ALOX15CYP3A4
SCHEMBL16924853 0.78 LMNA (0.67) CHRNA7SIGMAR1DRD2ALOX15CYP3A4
SCHEMBL576454 0.78 LMNA (0.67) CHRNA7SIGMAR1DRD2ALOX15CYP3A4
SCHEMBL385012 0.78 — —
SCHEMBL19962181 0.76 ADRB1 (0.53) TSHRSMN1; SMN2KMT2AALDH1A1LMNA

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
US-8197722-B2 Irradiating the compound (containing two electron donor groups and a bridge of pi-conjugated bonds containing electron donor groups) with light, and the compound is converted to a multi-photon electronically excited state THE CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2012-06-12 — — US disclosed
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