Piperazine

Piperazine

SCHEMBL192250

C1CNCCN1.c1cncnc1

nearest known ligand 0.40

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 17)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 1/20 0.40
MAPT P10636 1/20 0.40
PDE4A P27815 1/20 0.40
KDR P35968 1/20 0.40
CHRNB2 P17787 4/20 0.34
CHRNA4 P43681 4/20 0.34
CXCR4 P61073 1/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
TSHR P16473 1/20 0.33
NAPRT Q6XQN6 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
KDM4E B2RXH2 1/20 0.32
ALDH1A1 P00352 1/20 0.32
ADRB2 P07550 1/20 0.32
NCF1 P14598 1/20 0.32
PLD1 Q13393 1/20 0.32
CYP2A6 P11509 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
Piperazine SCHEMBL28605103 1.00 HIF1A (0.40) HIF1AMAPTPDE4AKDRCHRNB2
Piperazine SCHEMBL28017070 0.97 HIF1A (0.38) HIF1AMAPTPDE4AKDRCHRNB2
Piperazine SCHEMBL27991446 0.97 HIF1A (0.38) HIF1AMAPTPDE4AKDRCHRNB2
Piperazine SCHEMBL27985317 0.97 HIF1A (0.38) HIF1AMAPTPDE4AKDRCHRNB2
Piperidine SCHEMBL28992046 0.89 ALDH1A1 (0.47) HIF1AMAPTPDE4AKDRCHRNB2
Piperazine SCHEMBL3951824 0.89 TSHR (0.33) HIF1AMAPTPDE4AKDRCHRNB2
Pyrimidine SCHEMBL20897915 0.88 TSHR (0.30) TSHRNAPRTTDP1
Pyrimidine SCHEMBL21046656 0.88 ALDH1A1 (0.44) CHRNB2CHRNA4CXCR4SMN1; SMN2TSHR
Piperazine SCHEMBL28203228 0.87 HIF1A (0.30) HIF1AMAPTPDE4AKDR
Piperidine SCHEMBL1385062 0.85 ALDH1A1 (0.50) CHRNB2CHRNA4CXCR4SMN1; SMN2ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114414707-B Method and kit for detecting 19 drugs and metabolites thereof in blood by liquid chromatography tandem mass spectrometry 北京和合医学诊断技术股份有限公司 2022-07-22 CN claimed
CN-113024536-B 5-aminothiazole methanamide compound containing pyrimidine-piperazine ring and preparation method and application thereof 湖南师范大学 2022-05-27 CN claimed
CN-114414707-A Method and kit for detecting 19 drugs and metabolites thereof in blood by liquid chromatography tandem mass spectrometry 北京和合医学诊断技术股份有限公司 2022-04-29 CN claimed
CN-113248518-B Pyrimidine piperazine derivative and preparation method and application thereof 山东大学 2022-03-25 CN claimed
CN-113248518-A Pyrimidine piperazine derivative and preparation method and application thereof 山东大学 2021-08-13 CN claimed
CN-113024536-A 5-aminothiazole methanamide compound containing pyrimidine-piperazine ring and preparation method and application thereof 湖南师范大学 2021-06-25 CN claimed
CN-107365274-B pyrimidine piperazine amide compound and application thereof 广州医大科技发展有限公司 2019-11-26 CN claimed
US-10433544-B2 Herbicide UNIVERSITY OF KENTUCKY RESEARCH FOUNDATION (US) 2019-10-08 US claimed
CN-109517594-A Electroluminescent organic material and device 环球展览公司 2019-03-26 CN claimed
US-10227343-B2 Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction VANDERBILT UNIVERSITY (US) 2019-03-12 US claimed
WO-2016123627-A1 ISOQUINILINE AND NAPTHALENE-SUBSTITUTED COMPOUNDS AS MGLUR4 ALLOSTERIC POTENTIATORS, COMPOUNDS, AND METHODS OF TREATING NEUROLOGICAL DYSFUNCTION VANDERBILT UNIVERSITY (US) 2016-08-04 WO claimed
WO-2016115272-A1 BENZOTHIAZOLE AND BENZISOTHIAZOLE-SUBSTITUTED COMPOUNDS AS MGLUR4 ALLOSTERIC POTENTIATORS, COMPOSITIONS, AND METHODS OF TREATING NEUROLOGICAL DYSFUNCTION VANDERBILT UNIVERSITY (US) 2016-07-21 WO claimed
US-8211914-B2 Inhibitors of diacylglycerol acyltransferase MADRIGAL PHARMACEUTICALS, INC. (US) 2012-07-03 US claimed
CN-102245024-A Inhibitors of diacylglycerol aclytransferase VIA PHARMACEUTICALS INC 2011-11-16 CN claimed
US-20100152445-A1 Inhibitors of Diacylglycerol Acyltransferase MADRIGAL PHARMACEUTICALS, INC. 2010-06-17 US claimed
US-7629364-B2 Compounds that abrogate DNA-damage-induced cell cycle G2 checkpoint and/or augment anti-cancer activity of DNA-damaging treatments CANBAS CO., LTD. (JP) 2009-12-08 US claimed
CN-101318935-A Method for preparing hydrochloric 1-(2-pyrimidine) diethylenediamine compound NANTONG KANGXING PHARMACEUTICA (CN) 2008-12-10 CN claimed
CN-101316901-A Dye-attached and/or surface-modified pigments SOANE LAB LLC (US) 2008-12-03 CN claimed
US-20080293137-A1 COMPOUNDS THAT ABROGATE DNA DAMAGE INDUCED CELL CYCLE G2 CHECKPOINT AND/OR AUGMENT ANTI-CANCER ACTIVITY OF DNA-DAMAGING TREATMENTS CANBAS CO., LTD. (JP) 2008-11-27 US claimed
CN-101250184-A Method for synthesizing 1-(2-pyrimidine) piperazine TAICANG QIANJING CHEMICAL INDU (CN) 2008-08-27 CN claimed

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

For each of this compound's patents that has machine-readable text (3 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-20080293137-A1 COMPOUNDS THAT ABROGATE DNA DAMAGE INDUCED CELL CYCLE G2 CHECKPOINT AND/OR AUGMENT ANTI-CANCER ACTIVITY OF DNA-DAMAGING TREATMENTS CDC25C, CHEK1, CDC25A HIF1A 756/4885MAPT 4441/4885PDE4A 1739/4885
US-20100152445-A1 Inhibitors of Diacylglycerol Acyltransferase DGAT2, DGAT1, ACAT2 HIF1A 3758/4885MAPT 3731/4885PDE4A 781/4885
US-10227343-B2 Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction GRIA4, GRM4, GRIK4 HIF1A 3879/4885MAPT 984/4885PDE4A 258/4885

“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.