SCHEMBL6616565

SCHEMBL6616565

Nc1cccc(-c2ccc(CCN3CCN(CC(=O)c4ccc(Cl)cc4)CC3)cc2)n1

nearest known ligand 0.83

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOS1 P29475 7/20 0.83
NOS3 P29474 6/20 0.83
CHRM2 P08172 1/20 0.83
CHRM4 P08173 1/20 0.83
DRD2 P14416 3/20 0.52
HTR1A P08908 1/20 0.52
HTR2A P28223 1/20 0.52
LMNA P02545 2/20 0.48
KDM4E B2RXH2 1/20 0.48
ALDH1A1 P00352 1/20 0.48
MAPT P10636 1/20 0.48
HPGD P15428 1/20 0.48
RAB9A P51151 1/20 0.48
THRB P10828 1/20 0.45
KDR P35968 1/20 0.42
EBP Q15125 1/20 0.42
SIGMAR1 Q99720 1/20 0.42
PRCP P42785 1/20 0.41
DRD4 P21917 2/20 0.41
AVPR1B P47901 2/20 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
SCHEMBL6620545 0.91 NOS1 (1.00) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6617436 0.90 NOS1 (0.83) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6620863 0.90 NOS1 (0.83) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6623521 0.87 NOS1 (0.78) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6618617 0.84 NOS1 (0.85) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL27613058 0.83 NOS1 (0.61) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL27554919 0.81 NOS1 (0.63) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6622079 0.79 NOS1 (0.78) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL27554920 0.79 NOS1 (0.66) NOS1NOS3CHRM2CHRM4DRD2
SCHEMBL6618161 0.79 NOS1 (1.00) NOS1NOS3CHRM2CHRM4DRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20040229911-A1 New pharmaceutical combinations for NOS inhibitors PFIZER INC 2004-11-18 US claimed
US-20040229911-A1 New pharmaceutical combinations for NOS inhibitors PFIZER INC 2004-11-18 US disclosed
EP-1471055-A1 6-phenylpyridyl-2-amine derivatives PFIZER INC. (US) 2004-10-27 EP disclosed
EP-0891332-B1 6-PHENYLPYRIDYL-2-AMINE DERIVATIVES PFIZER (US) 2004-03-17 EP disclosed
US-20020151572-A1 PHARMACEUTICAL USES FOR NOS INHIBITORS LOWE JOHN A (US) 2002-10-17 US disclosed
US-6465491-B2 NITRIC OXIDE SYNTHASE INHIBITOR; NERVOUS SYSTEM DISORDERS PFIZER INC. 2002-10-15 US disclosed
US-20010034348-A1 6-phenylpyridyl-2-amine derivatives LOWE JOHN A (US) 2001-10-25 US disclosed
US-6235747-B1 NITRIC OXIDE SYNTHASE INHIBITOR PFIZER INC. 2001-05-22 US 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 (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-20010034348-A1 6-phenylpyridyl-2-amine derivatives NOS2, NOS3, NOS1 NOS1 3/4885NOS3 2/4885CHRM2 151/4885
US-20020151572-A1 PHARMACEUTICAL USES FOR NOS INHIBITORS NOS1, NOS3, NOS2 NOS1 1/4885NOS3 2/4885CHRM2 284/4885
US-20040229911-A1 New pharmaceutical combinations for NOS inhibitors NOS1, NOS3, NPBWR1 NOS1 1/4885NOS3 2/4885CHRM2 762/4885

“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.