Piperazine

Piperazine

SCHEMBL1442999

C1CNCCN1.CCCCCc1ccon1

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR1

The experimentally established mechanism targets of Piperazine. 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
KCNH2 Q12809 1/20 0.41
CYP1A2 P05177 1/20 0.36
CYP2D6 P10635 1/20 0.36
CYP19A1 P11511 1/20 0.36
CYP2C9 P11712 1/20 0.36
CYP2C19 P33261 1/20 0.36
PPARA Q07869 1/20 0.35
TDP1 Q9NUW8 1/20 0.34
L3MBTL1 Q9Y468 1/20 0.34
ATM Q13315 1/20 0.34
MIF P14174 1/20 0.34
NPC1 O15118 1/20 0.33
PKM P14618 1/20 0.33
HTR2A P28223 1/20 0.32
HTR2C P28335 1/20 0.32
HTR2B P41595 1/20 0.32
CHRM2 P08172 1/20 0.31
CHRM4 P08173 1/20 0.31
CHRM5 P08912 1/20 0.31
CHRM1 P11229 1/20 0.31

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
SCHEMBL1221781 0.89 KCNH2 (0.48) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL20209685 0.88 KCNH2 (0.52) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL28018296 0.88 KCNH2 (0.52) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL21186452 0.88 KCNH2 (0.52) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL21645767 0.88 KCNH2 (0.52) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
Alcohol SCHEMBL22495162 0.84 KCNH2 (0.44) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL6049592 0.84
Ammonia Solution, Strong SCHEMBL6014423 0.82 CYP1A2 (0.42) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL29244185 0.77 MIF (0.36) KCNH2CYP1A2CYP2D6CYP19A1CYP2C9
SCHEMBL22266323 0.76 SIGMAR1 (0.46) KCNH2CYP1A2CYP2D6L3MBTL1NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8629149-B2 Oxopiperazine derivatives for the treatment of pain and epilepsy ZALICUS PHARMACEUTICALS LTD. (CA) 2014-01-14 US disclosed
CN-102656151-A Substituted heterocyclic derivatives for the treatment of pain and epilepsy ZALICUS PHARMACEUTICALS LTD 2012-09-05 CN disclosed
US-20120220605-A1 OXOPIPERAZINE DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY ZALICUS PHARMACEUTICALS LTD. (CA) 2012-08-30 US disclosed
US-20120220603-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY ZALICUS PHARMACEUTICALS LTD. (CA) 2012-08-30 US disclosed
EP-2473488-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY Zalicus Pharmaceuticals Ltd. (CA) 2012-07-11 EP disclosed
WO-2011026241-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY ZALICUS PHARMACEUTICALS LTD. (CA) 2011-03-10 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20120220603-A1 SUBSTITUTED HETEROCYCLIC DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY CACNA1B, SCN1A, CACNA1I KCNH2 40/4885CYP1A2 286/4885CYP2D6 688/4885
US-20120220605-A1 OXOPIPERAZINE DERIVATIVES FOR THE TREATMENT OF PAIN AND EPILEPSY CACNA1H, CACNG7, CACNA1I KCNH2 17/4885CYP1A2 1641/4885CYP2D6 1693/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.