SCHEMBL1701240

SCHEMBL1701240

CC(N)C(c1ccccc1)(c1ccccc1)c1ccccc1Cl

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KCNN4 O15554 6/20 0.53
KIF11 P52732 1/20 0.43
KCNA3 P22001 2/20 0.41
CYP1A2 P05177 3/20 0.41
CYP2D6 P10635 3/20 0.41
TSHR P16473 3/20 0.41
CYP3A4 P08684 3/20 0.41
SLC6A2 P23975 3/20 0.41
SLC6A4 P31645 3/20 0.41
SLC6A3 Q01959 3/20 0.41
LMNA P02545 3/20 0.41
HTR2A P28223 2/20 0.41
HTR2C P28335 2/20 0.41
OPRK1 P41145 2/20 0.41
KCNH2 Q12809 2/20 0.41
NFKB1 P19838 2/20 0.41
GLA P06280 2/20 0.41
MAOA P21397 2/20 0.41
ADRA1A P35348 1/20 0.41
MEN1 O00255 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
SCHEMBL5967507 0.81 KCNN4 (0.49) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL4855348 0.80 KCNN4 (0.43) KCNN4CYP1A2CYP2D6SLC6A2SLC6A4
SCHEMBL27824023 0.79 KCNN4 (0.53) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL16416723 0.74 KCNN4 (0.45) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL27183395 0.73 KCNN4 (0.57) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL7901027 0.72 KCNN4 (0.42) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL2406097 0.71 KCNN4 (0.46) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL27459558 0.71 KCNN4 (0.72) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL27558142 0.71 KCNN4 (0.64) KCNN4KIF11KCNA3CYP1A2CYP2D6
SCHEMBL1001586 0.70 KCNN4 (1.00) KCNN4KIF11KCNA3CYP1A2CYP2D6

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
EP-2566883-A1 NOVEL PROCESS FOR THE PREPARATION OF LEUPROLIDE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF Mylan Laboratories, Limited (IN) 2013-03-13 EP claimed
US-20130060004-A1 Novel Process For The Preparation Of Leuprolide And Its Pharmaceutically Acceptable Salts Thereof MYLAN LABORATORIES LIMITED (IN) 2013-03-07 US claimed
WO-2011148384-A1 NOVEL PROCESS FOR THE PREPARATION OF LEUPROLIDE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF MATRIX LABORATORIES LTD (IN) 2011-12-01 WO claimed
EP-2566883-A1 NOVEL PROCESS FOR THE PREPARATION OF LEUPROLIDE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF Mylan Laboratories, Limited (IN) 2013-03-13 EP disclosed
US-20130060004-A1 Novel Process For The Preparation Of Leuprolide And Its Pharmaceutically Acceptable Salts Thereof MYLAN LABORATORIES LIMITED (IN) 2013-03-07 US disclosed
WO-2011148384-A1 NOVEL PROCESS FOR THE PREPARATION OF LEUPROLIDE AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF MATRIX LABORATORIES LTD (IN) 2011-12-01 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-20130060004-A1 Novel Process For The Preparation Of Leuprolide And Its Pharmaceutically Acceptable Salts Thereof LPXN, GNRHR, VIP KCNN4 699/4885KIF11 1406/4885KCNA3 3339/4885

“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.