SCHEMBL191697

SCHEMBL191697

Cc1nc2cnc3cccnc3c2n1CC(C)C

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 4/20 0.39
SMN1; SMN2 Q16637 2/20 0.39
HTT P42858 2/20 0.39
TSHR P16473 1/20 0.39
HTR2A P28223 2/20 0.39
HTR2B P41595 2/20 0.39
HTR2C P28335 1/20 0.39
CCR1 P32246 1/20 0.37
CCR5 P51681 1/20 0.37
CCR8 P51685 1/20 0.37
ALDH1A1 P00352 3/20 0.36
APAF1 O14727 1/20 0.36
KDM4E B2RXH2 2/20 0.35
TNF P01375 1/20 0.35
HPGD P15428 1/20 0.35
POLB P06746 1/20 0.34
HRH2 P25021 1/20 0.34
ADRA1D P25100 1/20 0.34
ADORA2A P29274 1/20 0.34
ADRA1A P35348 1/20 0.34

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
SCHEMBL192522 0.84 TSHR (0.42) LMNASMN1; SMN2TSHRHTR2AHTR2B
SCHEMBL1490884 0.83 TP53 (0.36) LMNASMN1; SMN2HTTHTR2AHTR2B
SCHEMBL4056414 0.81 ALDH1A1 (0.41) LMNASMN1; SMN2HTTTSHRALDH1A1
SCHEMBL6724014 0.81 SMN1; SMN2 (0.47) LMNASMN1; SMN2HTTTSHRHTR2A
SCHEMBL3355085 0.80 TLR7 (0.45) KDM4EPDE4DTLR7
Sotirimod SCHEMBL29395045 0.79 TLR7 (0.50) LMNAHTR2AHTR2BHTR2CPOLB
Sotirimod SCHEMBL191424 0.79 TLR7 (0.50) LMNAHTR2AHTR2BHTR2CPOLB
SCHEMBL841480 0.78 ALDH1A1 (0.36) LMNASMN1; SMN2HTTHTR2AHTR2B
SCHEMBL14000523 0.76 ALDH1A1 (0.33) LMNASMN1; SMN2HTTTSHRHTR2A
SCHEMBL191733 0.76 HTR2A (0.33) LMNASMN1; SMN2HTTTSHRHTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8436176-B2 Process for preparing 2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine MEDICIS PHARMACEUTICAL CORPORATION (US) 2013-05-07 US claimed
EP-1833827-B9 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE MEDA AB (SE) 2012-01-04 EP claimed
EP-1833827-B1 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE MEDA AB (SE) 2011-05-25 EP claimed
EP-1865957-A4 METHOD OF TREATING ACTINIC KERATOSIS MEDA AB (SE) 2009-05-06 EP claimed
US-20080306266-A1 Process for Preparing 2-Methyl-1-(2-Methylpropyl)-1H-Imidazo[4,5-C][1,5]Naphthyridin-4-Amine 3M INNOVATIVE PROPERTIES COMPANY 2008-12-11 US claimed
EP-1865957-A2 METHOD OF TREATING ACTINIC KERATOSIS Meda AB (SE) 2007-12-19 EP claimed
EP-1833827-A2 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZOÝ4,5-C¨Ý1,5¨NAPHTHYRIDIN-4-AMINE 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-09-19 EP claimed
WO-2006099275-A2 METHOD OF TREATING ACTINIC KERATOSIS 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-09-21 WO claimed
WO-2006074046-A2 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE 3M INNOVATIVE PROPERTIES COMPANY (US) 2006-07-13 WO claimed
US-8436176-B2 Process for preparing 2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine MEDICIS PHARMACEUTICAL CORPORATION (US) 2013-05-07 US disclosed
US-8436176-B2 Process for preparing 2-methyl-1-(2-methylpropyl)-1H-imidazo[4,5-c][1,5]naphthyridin-4-amine MEDICIS PHARMACEUTICAL CORPORATION (US) 2013-05-07 US disclosed
EP-1833827-B9 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE MEDA AB (SE) 2012-01-04 EP disclosed
EP-1833827-B9 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE MEDA AB (SE) 2012-01-04 EP disclosed
EP-1833827-B1 PROCESS FOR PREPARING 2-METHYL-1-(2-METHYLPROPYL)-1H-IMIDAZO[4,5-C][1,5]NAPHTHYRIDIN-4-AMINE MEDA AB (SE) 2011-05-25 EP disclosed
US-6514985-B1 Induce the biosynthesis of cytokines such as interferon and tumor necrosis factor; exhibit antiviral and antitumor properties 3M INNOVATIVE PROPERTIES COMPANY 2003-02-04 US disclosed
US-20020173653-A1 Imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY 2002-11-21 US disclosed
US-20020173654-A1 Imidazonaphthyridines 3M INNOVATIVE PROPERTIES COMPANY 2002-11-21 US disclosed
US-6194425-B1 VIRICIDES, ANTITUMOR AGENTS 3M INNOVATIVE PROPERTIES COMPANY 2001-02-27 US disclosed
EP-1040112-A1 IMIDAZONAPHTHYRIDINES AND THEIR USE IN INDUCING CYTOKINE BIOSYNTHESIS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 2000-10-04 EP disclosed
WO-1999029693-A1 IMIDAZONAPHTHYRIDINES AND THEIR USE IN INDUCING CYTOKINE BIOSYNTHESIS MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1999-06-17 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 (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-20020173653-A1 Imidazonaphthyridines IFNG, IRF3, IFNAR1 LMNA 3209/4885SMN1; SMN2 4092/4885HTT 3763/4885
US-20020173654-A1 Imidazonaphthyridines IFNG, IRF3, IFNAR1 LMNA 3209/4885SMN1; SMN2 4092/4885HTT 3763/4885
US-20080306266-A1 Process for Preparing 2-Methyl-1-(2-Methylpropyl)-1H-Imidazo[4,5-C][1,5]Naphthyridin-4-Amine DNMT1, NT5C, JMJD1C LMNA 166/4885SMN1; SMN2 448/4885HTT 2585/4885

“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.