SCHEMBL7230380

SCHEMBL7230380

C=C(CN1CCCCC1)CN1CCNC1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SIGMAR1 Q99720 3/20 0.37
CHRM5 P08912 2/20 0.37
CHRM3 P20309 2/20 0.37
GAA P10253 1/20 0.35
CXCR4 P61073 3/20 0.33
ALDH1A1 P00352 3/20 0.33
CA2 P00918 1/20 0.31
CHKA P35790 1/20 0.31
STAT6 P42226 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
MEN1 O00255 2/20 0.30
KMT2A Q03164 2/20 0.30
CHRM2 P08172 1/20 0.30
CHRM1 P11229 1/20 0.30
ADRA2C P18825 1/20 0.30
CCR2 P41597 1/20 0.30
CXCL12 P48061 1/20 0.30
BLM P54132 1/20 0.30
TDP1 Q9NUW8 1/20 0.30
HRH3 Q9Y5N1 1/20 0.30

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
SCHEMBL7230790 0.98 CHRM5 (0.37) SIGMAR1CHRM5CHRM3GAACXCR4
SCHEMBL7222004 0.90 SIGMAR1 (0.43) SIGMAR1CHRM5CHRM3GAACXCR4
SCHEMBL7225311 0.90 CHRM5 (0.39) SIGMAR1CHRM5CHRM3CXCR4ALDH1A1
SCHEMBL7223824 0.90 CHRM5 (0.33) SIGMAR1CHRM5CHRM3CXCR4ALDH1A1
SCHEMBL7694509 0.88 CHRM5 (0.44) SIGMAR1CHRM5CHRM3GAACXCR4
SCHEMBL7224032 0.81 KDM4E (0.40) CHRM5CHRM3ALDH1A1SMN1; SMN2HTT
SCHEMBL7229675 0.81 CHRM5 (0.38) SIGMAR1CHRM5CHRM3GAACXCR4
SCHEMBL7229670 0.81 CHRM5 (0.38) SIGMAR1CHRM5CHRM3GAACXCR4
SCHEMBL7222024 0.81 CHRM5 (0.44) SIGMAR1CHRM5CHRM3CXCR4ALDH1A1
SCHEMBL7221817 0.81 GAA (0.48) CHRM5GAAALDH1A1STAT6SMN1; SMN2

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-6552226-B1 Rapid; low temperature; one pot synthesis; reduced catalytic quantities of such as lewis acid and tertiary amine; entiomerically pure products THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2003-04-22 US disclosed
WO-2002026683-A1 TANDEM ACYL-CLAISEN REARRANGEMENT IN THE PREPARATION OF CHIRAL PRODUCTS THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (US) 2002-04-04 WO disclosed