SCHEMBL7221409

SCHEMBL7221409

C=CCN1CCNC(c2ccccc2)C1

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD1 P21728 10/20 0.45
KDM4E B2RXH2 3/20 0.45
MTOR P42345 3/20 0.45
CYP2D6 P10635 3/20 0.45
THPO P40225 3/20 0.45
HIF1A Q16665 3/20 0.45
HSD17B10 Q99714 3/20 0.45
MAPT P10636 3/20 0.45
TDP1 Q9NUW8 1/20 0.45
LMNA P02545 2/20 0.44
BLM P54132 2/20 0.44
PMP22 Q01453 2/20 0.44
DRD2 P14416 6/20 0.43
DRD3 P35462 2/20 0.43
CYP1A2 P05177 2/20 0.41
CYP3A4 P08684 2/20 0.41
CYP2C9 P11712 2/20 0.41
ALOX15 P16050 2/20 0.41
NFKB1 P19838 1/20 0.41
TSHR P16473 1/20 0.41

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
SCHEMBL7013419 0.80 GSK3B (0.42) DRD1LMNADRD2DRD3
SCHEMBL3272931 0.78 SIGMAR1 (0.54) CYP2D6HIF1ACYP1A2CYP3A4CYP2C9
SCHEMBL3272922 0.78 SIGMAR1 (0.54) CYP2D6HIF1ACYP1A2CYP3A4CYP2C9
SCHEMBL3277741 0.78 SIGMAR1 (0.54) CYP2D6HIF1ACYP1A2CYP3A4CYP2C9
SCHEMBL7014512 0.77 SLC18A3 (0.51) DRD1LMNADRD2DRD3GAA
SCHEMBL20449122 0.76 KDM1A (0.43) KDM4E
SCHEMBL27986060 0.76 TMEM97 (0.40) KDM4ETSHR
SCHEMBL20449121 0.76 KDM1A (0.43) KDM4E
SCHEMBL1546984 0.74 DRD2 (0.53) DRD1KDM4EMTORCYP2D6THPO
SCHEMBL1546980 0.74 DRD2 (0.53) DRD1KDM4EMTORCYP2D6THPO

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6603003-B2 Reacting ester with substituted or unsubstituted ethylenediamine to give 3,4-dehydropiperazine-2-one and reacting 3,4-dehydropiperazine-2-one with reducing agent to yield piperazine derivative SUN PHARMACEUTICAL INDUSTRIES LTD (IN) 2003-08-05 US disclosed
US-20020095038-A1 Novel method for the preparation of piperazine and its derivatives SUN PHARMACEUTICAL INDUSTRIES LTD (IN) 2002-07-18 US disclosed
WO-2002038552-A1 A NOVEL METHOD FOR THE PREPARATION OF PIPERAZINE AND ITS DERIVATIVES SUN PHARMACEUTICAL INDUSTRIES LTD. (IN) 2002-05-16 WO disclosed
US-6162809-A Pyridylthio compounds for controlling helicobacter bacteria BYK GULDEN LOMBERG CHEMISCHE FABRIK GMBH (DE) 2000-12-19 US disclosed
EP-0891332-A1 6-PHENYLPYRIDYL-2-AMINE DERIVATIVES PFIZER INC. (US) 1999-01-20 EP disclosed
WO-1997036871-A1 6-PHENYLPYRIDYL-2-AMINE DERIVATIVES PFIZER INC. (US) 1997-10-09 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-20020095038-A1 Novel method for the preparation of piperazine and its derivatives DHPS, DRD4, CYP2E1 DRD1 5/4885KDM4E 525/4885MTOR 3151/4885

“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.