Piperazine

Piperazine

SCHEMBL4470404

C1CNCCN1.c1ccc(Nc2ncc[nH]2)cc1

nearest known ligand 0.49

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
ADRA2A P08913 6/20 0.49
ADRA2C P18825 6/20 0.49
ADRA1D P25100 5/20 0.49
ADRA1A P35348 5/20 0.49
ADRA1B P35368 5/20 0.49
TAAR1 Q96RJ0 3/20 0.45
CSNK2A1 P68400 1/20 0.41
POLB P06746 2/20 0.41
KMT2A Q03164 2/20 0.41
ALDH1A1 P00352 1/20 0.40
MTOR P42345 1/20 0.40
ADK P55263 1/20 0.40
NISCH Q9Y2I1 1/20 0.40
TTBK1 Q5TCY1 1/20 0.39
TTBK2 Q6IQ55 1/20 0.39
PAK4 O96013 1/20 0.38
HSD17B10 Q99714 1/20 0.38
MEN1 O00255 1/20 0.38
ITGB3 P05106 1/20 0.37
ITGAV P06756 1/20 0.37

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
SCHEMBL770786 0.91 ADRA2A (0.56) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL28046710 0.89 ADRA2A (0.55) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL28046796 0.89 ADRA2A (0.55) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL28046706 0.89 ADRA2A (0.55) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL21067687 0.78 ADRA2A (0.63) ADRA2AADRA2CADRA1DADRA1AADRA1B
Diphenylamine SCHEMBL27703830 0.73 HSD17B10 (0.71) POLBKMT2AALDH1A1HSD17B10MEN1
SCHEMBL14629679 0.72 ADRA2A (0.56) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL1842264 0.72 ADRA2A (0.56) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL5851701 0.72 ADRA2A (0.56) ADRA2AADRA2CADRA1DADRA1AADRA1B
SCHEMBL708660 0.71 ADRA2A (0.56) ADRA2AADRA2CADRA1DADRA1AADRA1B

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-7635697-B2 Farnesyl protein transferase inhibitors and methods for treating proliferative diseases SCHERING CORPORATION (US) 2009-12-22 US disclosed
EP-1833481-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS AND METHODS FOR TREATING PROLIFERATIVE DISEASES SCHERING CORPORATION (US) 2007-09-19 EP disclosed
US-20060211706-A1 Farnesyl protein transferase inhibitors and methods for treating proliferative diseases SCHERING CORPORATION 2006-09-21 US disclosed
WO-2006065794-A1 FARNESYL PROTEIN TRANSFERASE INHIBITORS AND METHODS FOR TREATING PROLIFERATIVE DISEASES SCHERING CORPORATION (US) 2006-06-22 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-20060211706-A1 Farnesyl protein transferase inhibitors and methods for treating proliferative diseases FNTB, FNTA, FDPS ADRA2A 4325/4885ADRA2C 4335/4885ADRA1D 4265/4885

“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.