SCHEMBL6272726

SCHEMBL6272726

CCCCn1c(N)nc2[nH]cnc2c1=O

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PDE4A P27815 7/20 0.49
▸ ADORA2A P29274 7/20 0.49
▸ PDE4B Q07343 7/20 0.49
▸ PDE4C Q08493 7/20 0.49
▸ PDE4D Q08499 7/20 0.49
▸ ADORA2B P29275 5/20 0.49
▸ ADORA3 P0DMS8 1/20 0.49
▸ USP2 O75604 3/20 0.44
▸ POLB P06746 3/20 0.44
▸ MEN1 O00255 2/20 0.44
▸ KMT2A Q03164 2/20 0.44
▸ KEAP1 Q14145 2/20 0.44
▸ NFE2L2 Q16236 2/20 0.44
▸ SMN1; SMN2 Q16637 2/20 0.44
▸ RGS12 O14924 1/20 0.44
▸ NPC1 O15118 1/20 0.44
▸ ALDH1A1 P00352 1/20 0.44
▸ RAB9A P51151 1/20 0.44
▸ BLM P54132 1/20 0.44
▸ CACNA1B Q00975 1/20 0.44

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
SCHEMBL8522266 0.96 ADORA2B (0.51) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL6272293 0.95 ADORA2B (0.53) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL4384737 0.95 ADORA2B (0.53) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL8536000 0.95 ADORA2B (0.53) PDE4AADORA2APDE4BPDE4CPDE4D
Hydrochloric Acid SCHEMBL258895 0.93 ADORA2B (0.52) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL667794 0.92 PDE4A (0.49) PDE4AADORA2APDE4BPDE4CPDE4D
Acetic Acid SCHEMBL4280715 0.89 ADORA2B (0.48) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL8196740 0.86 ADORA2B (0.37) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL874734 0.85 ADORA2A (0.45) PDE4AADORA2APDE4BPDE4CPDE4D
SCHEMBL3671337 0.83 PNP (0.37) PDE4AADORA2APDE4BPDE4CPDE4D

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1017394-B1 CYCLIN DEPENDENT KINASE INHIBITING PURINE DERIVATIVES CANCER REC TECH LTD (GB) 2005-12-07 — — EP disclosed
EP-1230267-A2 MEMBRANE TRANSLOCATING PEPTIDE DRUG DELIVERY SYSTEM O'Mahony, Daniel J. (IE) 2002-08-14 — — EP disclosed
US-6303618-B1 ADMINISTERING PURINE COMPOUND WHICH INHIBITS CYCLIC DEPENDENT KINASE ACTIVITY FOR THERAPY OF TUMOR OR OTHER CELL PROLIFERATION DISORDER CANCER RESEARCH CAMPAIGN TECHNOLOGY LIMITED (GB) 2001-10-16 — — US disclosed
CN-1067073-C Acyclic nucleoside derivatives MEDIVIR AB (CH) 2001-06-13 — — CN disclosed
WO-2001027154-A2 MEMBRANE TRANSLOCATING PEPTIDE DRUG DELIVERY SYSTEM MAHONY DANIEL J O (IE) 2001-04-19 — — WO disclosed
CN-1210537-A Acyclic nucleoside derivatives MEDIVIR AB (CH) 1999-03-10 — — CN disclosed
EP-0523100-A4 O?6 -BENZYLATED GUANINE, GUANOSINE AND 2'-DEOXYGUANOSINE COMPOUNDS POSSESSING O?6 -ALKYLGUANINE-DNA ALKYLTRANSFERASE DEPLETING ACTIVITY US HEALTH (US) 1993-03-17 — — EP disclosed
EP-0523100-A1 O?6 -BENZYLATED GUANINE, GUANOSINE AND 2'-DEOXYGUANOSINE COMPOUNDS POSSESSING O?6 -ALKYLGUANINE-DNA ALKYLTRANSFERASE DEPLETING ACTIVITY. US HEALTH (US) 1993-01-20 — — EP disclosed
WO-1991013898-A1 O6-BENZYLATED GUANINE, GUANOSINE AND 2'-DEOXYGUANOSINE COMPOUNDS POSSESSING O6-ALKYLGUANINE-DNA ALKYLTRANSFERASE DEPLETING ACTIVITY THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, UNITED STATES DEPARTMENT OF COMMERCE (US) 1991-09-19 — — WO disclosed
EP-0152316-B1 SUBSTITUTED BUTYL GUANINES AND THEIR UTILIZATION IN ANTIVIRAL COMPOSITIONS MERCK & CO. INC. (US) 1989-07-26 — — EP disclosed
EP-0152316-A1 Substituted butyl guanines and their utilization in antiviral compositions MERCK & CO. INC. (US) 1985-08-21 — — EP disclosed
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