Piperazine

Piperazine

SCHEMBL27271

C1CNCCN1.CS(=O)(=O)O

nearest known ligand 0.46

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
CYP3A4 P08684 2/20 0.46
LMNA P02545 1/20 0.46
GABRA1 P14867 1/20 0.46
TSHR P16473 1/20 0.46
GABRG2 P18507 1/20 0.46
NFKB1 P19838 1/20 0.46
GABRB3 P28472 1/20 0.46
GABRA5 P31644 1/20 0.46
GABRA3 P34903 1/20 0.46
GABRA2 P47869 1/20 0.46
GABRA6 Q16445 1/20 0.46
HIF1A Q16665 1/20 0.43
MAPT P10636 1/20 0.43
PDE4A P27815 1/20 0.43
KDR P35968 1/20 0.43
CA2 P00918 1/20 0.39
CXCR4 P61073 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
KDM4E B2RXH2 4/20 0.33
CA5A P35218 1/20 0.33

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
SCHEMBL2585493 1.00 CYP3A4 (0.46) CYP3A4LMNAGABRA1TSHRGABRG2
Piperazine SCHEMBL11121855 1.00 CYP3A4 (0.46) CYP3A4LMNAGABRA1TSHRGABRG2
Aziridine SCHEMBL4605466 0.96
Pyrrolidine SCHEMBL8652906 0.87 ALDH1A1 (0.47) CYP3A4LMNAGABRA1TSHRGABRG2
SCHEMBL28163184 0.87 LMNA (0.36) CYP3A4LMNAGABRA1TSHRGABRG2
Piperazine SCHEMBL27671947 0.86 LMNA (0.46) CYP3A4LMNAGABRA1TSHRGABRG2
Piperazine SCHEMBL27330293 0.86 LMNA (0.46) CYP3A4LMNAGABRA1TSHRGABRG2
Azetidine SCHEMBL29252035 0.86
Azetidine SCHEMBL5748083 0.86 CYP3A4 (0.39) CYP3A4LMNAGABRA1TSHRGABRG2
Sulfuric Acid SCHEMBL8300104 0.85 TSHR (0.50) CYP3A4LMNAGABRA1TSHRGABRG2

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 101 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2014037886-A1 PROCESS FOR THE PREPARATION OF LURASIDONE HYDROCHLORIDE RANBAXY LABORATORIES LIMITED (IN) 2014-03-13 WO claimed
CN-101068798-B Salts and crystals of 1-cyclopropylmethyl-4- [2- (3,3,5, 5-tetramethylcyclohexyl) phenyl ] piperazine EISAI R&D MAN CO LTD 2010-05-12 CN claimed
CN-101068798-A Salts and crystals of 1-cyclopropylmethyl-4- [ 2- (3,3,5, 5-tetramethylcyclohexyl) phenyl ] piperazine EISAI R&D MAN CO LTD (JP) 2007-11-07 CN claimed
CN-1089086-C Luminandide medicine MILLS RANDELL L (US) 2002-08-14 CN claimed
CN-119367311-A Doxazosin mesylate sustained release tablet and preparation method thereof 南京易亨制药有限公司 2025-01-28 CN disclosed
CN-117777116-A Preparation method of high-purity doxazosin mesylate F crystal form 合肥立方制药股份有限公司 2024-03-29 CN disclosed
CN-116133688-A Multilayer inhalation medicine 迈兰制药英国有限公司 2023-05-16 CN disclosed
CN-110283162-B Epidermal growth factor receptor inhibitor and application thereof 辽宁大学 2022-04-05 CN disclosed
CN-113750063-A Solid preparation of piperazine isethionate cetirizine and preparation method thereof 江苏食品药品职业技术学院 2021-12-07 CN disclosed
CN-108558865-B Derivative taking pyrido [2,3-d ] pyrimidine structure as mother nucleus, and preparation method and application thereof 辽宁大学 2021-06-01 CN disclosed
US-10695449-B2 Catalytic radiofluorination THE GENERAL HOSPITAL CORPORATION (US) 2020-06-30 US disclosed
CN-110325533-A INHIBITORS OF THE MENIN-MLL INTERACTION 生命医药有限责任公司 2019-10-11 CN disclosed
US-6448250-B1 INHIBITS THE ACTIVITY OF ONE OR MORE OF THE FOLLOWING MATRIX METALLOPROTEINASES: MMP-2, MMP-9, AND MMP-13, WHILE EXHIBITING SUBSTANTIALLY LESS INHIBITORY ACTIVITY AGAINST MMP-1 G. D. SEARLE & COMPANY 2002-09-10 US disclosed
EP-1157021-A1 SULFAMATO HYDROXAMIC ACID METALLOPROTEASE INHIBITOR G.D. SEARLE & CO. (US) 2001-11-28 EP disclosed
CN-1301149-A Lofuridine tablets UPJOHN CO (US) 2001-06-27 CN disclosed
WO-2000046221-A1 SULFAMATO HYDROXAMIC ACID METALLOPROTEASE INHIBITOR G.D. SEARLE & CO. (US) 2000-08-10 WO disclosed
CN-1221398-A Mannitol and its preparation BAYER AG (DE) 1999-06-30 CN disclosed
CN-87107548-A Strengthen the compositions of transdermal flux 1988-05-11 CN disclosed
CN-87104918-A The drug-containing fibers of controllable release 1988-01-27 CN disclosed
EP-0034284-B1 PIPERAZINE DERIVATIVE, PROCESSES FOR PREPARING THE SAME AND THERAPEUTIC COMPOSITIONS CONTAINING IT Tanabe Seiyaku Co., Ltd. (JP) 1983-10-05 EP 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-10695449-B2 Catalytic radiofluorination KCNJ5, KCNQ5, KCNK18 CYP3A4 2708/4885LMNA 3906/4885GABRA1 3449/4885

“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.