Piperazine

Piperazine

SCHEMBL7073764

C1CNCCN1.O=C(O)c1c[nH]c2ccccc12

nearest known ligand 0.65

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
HTR3E A5X5Y0 1/20 0.65
HTR3B O95264 1/20 0.65
HTR3A P46098 1/20 0.65
HTR3D Q70Z44 1/20 0.65
HTR3C Q8WXA8 1/20 0.65
GPR84 Q9NQS5 1/20 0.65
ALDH1A1 P00352 2/20 0.61
PBRM1 Q86U86 1/20 0.61
ATM Q13315 1/20 0.61
NPC1 O15118 2/20 0.58
RAB9A P51151 2/20 0.58
TDP1 Q9NUW8 1/20 0.58
NR4A2 P43354 2/20 0.57
ADAM17 P78536 1/20 0.57
MAPK1 P28482 1/20 0.56
CREBBP Q92793 1/20 0.56
CTNNB1 P35222 1/20 0.55
WNT3A P56704 1/20 0.55
KMT2A Q03164 3/20 0.54
MEN1 O00255 2/20 0.54

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
Piperidine SCHEMBL8707735 0.92 HTR3E (0.60) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL64182 0.91 GPR84 (0.77) GPR84ALDH1A1PBRM1ATMNPC1
Hydrochloric Acid SCHEMBL28246505 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
SCHEMBL29272694 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
SCHEMBL27656464 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
Hydrochloric Acid SCHEMBL29435427 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
Hydrochloric Acid SCHEMBL7437913 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
Ammonia Solution, Strong SCHEMBL27380523 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
SCHEMBL27837528 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1
Hydrochloric Acid SCHEMBL72812 0.89 GPR84 (0.74) GPR84ALDH1A1PBRM1ATMNPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20030073699-A1 Compounds and methods to treat cardiac failure and other disorders SCIOS, INC. 2003-04-17 US disclosed
US-6130235-A PIPERIDINE MOIETIES COUPLED TO INDOLE, BENZIMIDAZOLE OR BENZOTRIAZOLE. SCIOS INC. (US) 2000-10-10 US disclosed
EP-0922042-A1 NOVEL PIPERAZINE CONTAINING COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 1999-06-16 EP disclosed
WO-1998006715-A1 NOVEL PIPERAZINE CONTAINING COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 1998-02-19 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 (1 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-20030073699-A1 Compounds and methods to treat cardiac failure and other disorders RCOR1, NR3C2, CNR1 HTR3E 397/4885HTR3B 216/4885HTR3A 453/4885

“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.