SCHEMBL6482143

SCHEMBL6482143

O=C(O)COCCN1CCNCC1C(c1ccccc1)c1ccc(Cl)cc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ HRH1 P35367 4/20 0.54
▸ DRD3 P35462 3/20 0.54
▸ KCNH2 Q12809 3/20 0.54
▸ SLC6A2 P23975 3/20 0.54
▸ SLC6A4 P31645 3/20 0.54
▸ SLC6A3 Q01959 3/20 0.54
▸ HRH2 P25021 2/20 0.54
▸ HTR2A P28223 2/20 0.54
▸ HTR2B P41595 2/20 0.54
▸ USP2 O75604 2/20 0.54
▸ TDP1 Q9NUW8 2/20 0.54
▸ TEK Q02763 1/20 0.54
▸ CHRM2 P08172 2/20 0.39
▸ ADRA2A P08913 2/20 0.39
▸ ADRA1A P35348 2/20 0.39
▸ CYP2D6 P10635 2/20 0.39
▸ ABCB11 O95342 1/20 0.39
▸ DRD2 P14416 1/20 0.39
▸ ADRA2B P18089 1/20 0.39
▸ ADRA2C P18825 1/20 0.39

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
Hydrochloric Acid SCHEMBL5957369 0.99 HRH1 (0.55) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL6475552 0.92 HRH1 (0.45) HRH1DRD3KCNH2SLC6A2SLC6A4
Hydrochloric Acid SCHEMBL27546451 0.84 HRH1 (0.38) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL10931334 0.83 TDP1 (0.39) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL5683230 0.82 TDP1 (0.41) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL16757280 0.80 TDP1 (0.46) DRD3KCNH2SLC6A2SLC6A4SLC6A3
SCHEMBL16757387 0.78 TDP1 (0.42) DRD3KCNH2SLC6A2SLC6A4SLC6A3
SCHEMBL6634453 0.76 HRH1 (0.54) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL7115205 0.75 HRH1 (0.42) HRH1DRD3KCNH2SLC6A2SLC6A4
SCHEMBL9844393 0.74 OPRD1 (0.42) SLC6A4TDP1OPRD1OPRM1

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-6908999-B2 Hydrolysis of N,N-disubstituted (2-(4-(alpha-phenyl-p-chloro-benzyl)piperazin-1-yl)ethoxy)acetamide, to form cetirizine and salts, used as antiallergens EGIS GYOGYSZERGYAR RT. (HU) 2005-06-21 — — US disclosed
US-6245353-B1 MIXING WITH EFFERVESCENT BASE ASTA MEDICA AG (DE) 2001-06-12 — — US disclosed
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