Perazine

Perazine

SCHEMBL7654455

CN1CCN(CCCN2c3ccccc3Sc3ccccc32)CC1.O=S(=O)(O)CCS(=O)(=O)O

nearest known ligand 0.82

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

The experimentally established mechanism targets of Perazine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD2 known ✓ P14416 4/20 0.65
CYP3A4 P08684 5/20 0.82
MAPT P10636 5/20 0.82
MAPK1 P28482 5/20 0.82
TP53 P04637 4/20 0.82
KDM4E B2RXH2 3/20 0.82
RAD52 P43351 3/20 0.82
ALOX15 P16050 2/20 0.82
USP2 O75604 2/20 0.82
TDP1 Q9NUW8 2/20 0.82
L3MBTL1 Q9Y468 1/20 0.82
KDM1A O60341 10/20 0.78
LMNA P02545 5/20 0.66
CYP1A2 P05177 3/20 0.66
CYP2D6 P10635 3/20 0.66
HTR1A P08908 4/20 0.65
ADRA2A P08913 4/20 0.65
CHRM1 P11229 4/20 0.65
ADRA2C P18825 4/20 0.65
DRD1 P21728 4/20 0.65

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
Prochlorperazine SCHEMBL40855 0.91 MAPT (1.00) CYP3A4MAPTMAPK1TP53KDM4E
Prochlorperazine SCHEMBL30903938 0.91 MAPT (1.00) CYP3A4MAPTMAPK1TP53KDM4E
Perazine SCHEMBL147165 0.88 KDM1A (1.00) CYP3A4MAPTMAPK1TP53KDM4E
Perazine SCHEMBL29390464 0.88 KDM1A (1.00) CYP3A4MAPTMAPK1TP53KDM4E
Perazine SCHEMBL2237726 0.87 KDM1A (0.97) CYP3A4MAPTMAPK1TP53KDM4E
Perazine SCHEMBL6644457 0.87 KDM1A (0.97) CYP3A4MAPTMAPK1TP53KDM4E
Perazine SCHEMBL10531680 0.86 KDM1A (0.84) CYP3A4MAPTMAPK1TP53KDM4E
SCHEMBL6859184 0.86 KDM1A (0.94) CYP3A4MAPTMAPK1TP53KDM4E
Prochlorperazine SCHEMBL10891828 0.84 MAPT (0.90) CYP3A4MAPTMAPK1TP53KDM4E
Prochlorperazine SCHEMBL1527298 0.83 MAPT (0.89) CYP3A4MAPTMAPK1TP53KDM4E

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 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6491903-B1 NARROW MOLECULAR WEIGHT DISTRIBUTION SHELL-CORE POLYMERS HAVING HYDROPHILIC, CROSSLINKED PERMEABLE SHELLS AND HYDROPHOBIC CORES, USED FOR REDUCING BLOOD CHOLESTEROL AND BILE ACID UPTAKE IN INTERSTINES; DRUG DELIVERY WASHINGTON UNIVERSITY 2002-12-10 US disclosed
US-6383500-B1 Particles comprising amphiphilic copolymers, having a crosslinked shell domain and an interior core domain, useful for pharmaceutical and other applications WASHINGTON UNIVERSITY 2002-05-07 US disclosed
EP-0910351-A1 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. Searle & Co. (US) 1999-04-28 EP disclosed
EP-0907666-A1 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. Searle & Co. (US) 1999-04-14 EP disclosed
WO-1997049736-A2 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. SEARLE AND CO. (US) 1997-12-31 WO disclosed
WO-1997049387-A1 PARTICLES COMPRISING AMPHIPHILIC COPOLYMERS, HAVING A CROSS-LINKED SHELL DOMAIN AND AN INTERIOR CORE DOMAIN, USEFUL FOR PHARMACEUTICAL AND OTHER APPLICATIONS G.D. SEARLE AND CO. (US) 1997-12-31 WO disclosed
US-5082668-A Osmotic drug delivery ALZA CORPORATION (US) 1992-01-21 US disclosed