Piperazine

Piperazine

SCHEMBL5874627

C1CNCCN1.O=C(O)C(=O)O

nearest known ligand 0.50

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
HIF1A Q16665 1/20 0.50
MAPT P10636 1/20 0.50
PDE4A P27815 1/20 0.50
KDR P35968 1/20 0.50
TSHR P16473 2/20 0.45
GABRP O00591 1/20 0.45
GABRD O14764 1/20 0.45
GABRA1 P14867 1/20 0.45
GABRB1 P18505 1/20 0.45
GABRG2 P18507 1/20 0.45
GABRB3 P28472 1/20 0.45
GABRA5 P31644 1/20 0.45
GABRA3 P34903 1/20 0.45
GABRA2 P47869 1/20 0.45
GABRB2 P47870 1/20 0.45
GABRA4 P48169 1/20 0.45
GABRE P78334 1/20 0.45
PMP22 Q01453 1/20 0.45
GABRA6 Q16445 1/20 0.45
GABRG1 Q8N1C3 1/20 0.45

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
Piperazine SCHEMBL27437295 1.00 HIF1A (0.50) HIF1AMAPTPDE4AKDRTSHR
Piperazine SCHEMBL5874616 1.00 HIF1A (0.50) HIF1AMAPTPDE4AKDRTSHR
Oxalic Acid SCHEMBL4602641 0.89 CXCR4 (0.60) HIF1AMAPTPDE4AKDRTSHR
Piperazine SCHEMBL5875145 0.87 HIF1A (0.55) HIF1AMAPTPDE4AKDRTSHR
Piperazine SCHEMBL3794325 0.87 HIF1A (0.55) HIF1AMAPTPDE4AKDRTSHR
Oxalic Acid SCHEMBL27344596 0.85 GABRP (0.35) HIF1AMAPTPDE4AKDRTSHR
Oxalic Acid SCHEMBL3717458 0.85 ALDH1A1 (0.53) HIF1AMAPTPDE4AKDRTSHR
Piperazine SCHEMBL2727552 0.83 HIF1A (0.50) HIF1AMAPTPDE4AKDRTSHR
Oxalic Acid SCHEMBL27608440 0.83 SLC6A1 (0.43) MAPTTSHRGABRPGABRDGABRA1
Bicarbonate SCHEMBL9715355 0.82

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110114051-B Antimicrobial compositions 联合利华知识产权控股有限公司 2022-04-08 CN claimed
CN-102123995-A Phenyl-alkyl piperazines with TNF modulating activity SANOFI AVENTIS 2011-07-13 CN claimed
CN-1227241-C Having 5-hydroxytryptamine 1AReceptor-active arylpiperazines LILLY CO ELI (US) 2005-11-16 CN claimed
CN-1290258-A Aryl piperazine compounds with 5-hydroxytryptamine 1A receptor activity LILLY CO ELI (US) 2001-04-04 CN claimed
JP-56034735-A None JP disclosed
CN-110114051-B Antimicrobial compositions 联合利华知识产权控股有限公司 2022-04-08 CN disclosed
CN-112888310-A Additive for stabilizing polyacrylamide copolymer solutions under high shear conditions 巴斯夫欧洲公司 2021-06-01 CN disclosed
CN-102471206-B Novel herbicides SYNGENTA LTD 2014-08-20 CN disclosed
CN-102065690-B Herbicidally effective 4-(3-alkyl sulfinyl benzoyl) pyrazoles BAYER CROPSCIENCE AG 2013-11-06 CN disclosed
CN-103380116-A 6-(2-aminophenyl)picolinates and their use as herbicides BAYER IP GMBH 2013-10-30 CN disclosed
CN-102741219-A Insecticidal compounds SYNGENTA PARTICIPATIONS AG 2012-10-17 CN disclosed
CN-102548397-A Pesticidal composition SYNGENTA PARTICIPATIONS AG 2012-07-04 CN disclosed
CN-1290258-A Aryl piperazine compounds with 5-hydroxytryptamine 1A receptor activity LILLY CO ELI (US) 2001-04-04 CN disclosed
CN-1283195-A 1-(2-naphthyl) and 1(2-azanaphthyl)-4-(1-phenylmethyl)piperazines being dopamine D4 receptor subtype ligands NEUROGEN CORP (US) 2001-02-07 CN disclosed
WO-1999031077-A1 ARYLPIPERAZINES HAVING ACTIVITY AT THE SEROTONIN 1A RECEPTOR ELI LILLY AND COMPANY (US) 1999-06-24 WO disclosed
CN-1099752-A Novel amidoalkyl-and imidoalkyl-piperazines ASTRA AB (SE) 1995-03-08 CN disclosed
US-4371668-A CARBOXYLIC ACID AMINE SALTS JAPAN SYNTHETIC RUBBER CO., LTD. (JP) 1983-02-01 US disclosed
US-4322319-A Rubber composition containing crosslinkable processing aid JAPAN SYNTHETIC RUBBER CO., LTD. (JP) 1982-03-30 US disclosed
US-4281085-A USING AN AMINE SALT OF A CARBOXYLIC ACID AS CROSSLINKING AGENT JAPAN SYNTHETIC RUBBER COMPANY, LTD. (JP) 1981-07-28 US disclosed
JP-S5634735-A RUBBER COMPOSITION JAPAN SYNTHETIC RUBBER CO LTD 1981-04-07 JP disclosed