SCHEMBL8074183

SCHEMBL8074183

[CH](c1ccccc1)C1CCNC1

nearest known ligand 0.54

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SLC18A3 Q16572 2/20 0.41
SIGMAR1 Q99720 1/20 0.41
HRH1 P35367 2/20 0.37
GBA1 P04062 1/20 0.37
KDM1A O60341 2/20 0.37
MAOA P21397 1/20 0.37
MAOB P27338 1/20 0.37
MEN1 O00255 1/20 0.35
LMNA P02545 1/20 0.35
CYP2D6 P10635 1/20 0.35
SCN1A P35498 1/20 0.35
KMT2A Q03164 1/20 0.35
SCN2A Q99250 1/20 0.35
SCN3A Q9NY46 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
SCHEMBL10681390 0.89 KDM1A (0.40) KDM1AMAOBKMT2A
SCHEMBL6002937 0.88 SLC18A3 (0.48) SLC18A3SIGMAR1HRH1GBA1KDM1A
SCHEMBL817532 0.81 KDM1A (0.46) KDM1AMAOAMAOBLMNA
SCHEMBL674275 0.75 MAOB (0.46) KDM1AMAOBLMNACYP2D6
SCHEMBL818902 0.72 KDM1A (0.51) SLC18A3SIGMAR1KDM1AMAOAMAOB
SCHEMBL20015683 0.72 KDM1A (0.51) SLC18A3SIGMAR1KDM1AMAOAMAOB
SCHEMBL27140897 0.72 KDM1A (0.51) SLC18A3SIGMAR1KDM1AMAOAMAOB
SCHEMBL5741697 0.72 GBA1 (0.46) SLC18A3SIGMAR1HRH1GBA1MAOB
SCHEMBL1119433 0.72 ALDH1A1 (0.42) MAOBLMNACYP2D6
SCHEMBL316481 0.72 POLB (0.45) MAOB

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-6030978-A EXHIBIT FUNGICIDAL EFFECT OR GROWTH-INHIBITORY EFFECT AGAINST FUNGI INCLUDING CUTANEOUS FILAMENTOUS FUNGUS, SUCH AS EPIDERMOPHYTON, MICROSPORUM, TRICHOPHYTON, SPOROTHRIX SCHENCKII, ASPERGILLUS OR CANDIDA; NONTOXICITY; HANWHA CORPORATION (KR) 2000-02-29 US claimed
US-6008356-A BRBERINE SALT DERIVATIVE IS REACTED WITH SODIUM TETRABORATE AND POTASSIUM CARBONATE IN ALCOHOL SOLVEANT TO FORM INTERMEDIATE, REACTING INTERMEDIATE WITH ALKYL SUBSTITUENT IN ACETONITRILE SOLVENT, OXIDIZING THE FORMED INTERMEDIATE HANWHA CORPORATION (KR) 1999-12-28 US claimed