SCHEMBL3036906

SCHEMBL3036906

Nc1nc(F)nc2c1ncn2[C@@H]1O[C@H](CO)CC1O

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.65
NT5E P21589 2/20 0.65
HIF1A Q16665 1/20 0.65
AHCY P23526 4/20 0.59
ADORA2A P29274 3/20 0.52
ADORA3 P0DMS8 2/20 0.52
ADORA1 P30542 2/20 0.52
ADORA2B P29275 2/20 0.52
CA5A P35218 1/20 0.52
PDE4D Q08499 2/20 0.49
PDE3A Q14432 2/20 0.49
PNP P00491 1/20 0.49
TP53 P04637 1/20 0.49
HTT P42858 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
RXFP1 Q9HBX9 1/20 0.49
PDE2A O00408 1/20 0.48
ADRA1A P35348 1/20 0.48
DNMT1 P26358 1/20 0.47
DNMT3B Q9UBC3 1/20 0.47

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
SCHEMBL21132768 1.00 LMNA (0.65) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL3036901 1.00 LMNA (0.65) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL29056321 0.90 NT5E (0.58) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL8923952 0.89 NT5E (0.62) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL26291351 0.89 NT5E (0.62) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL8923951 0.89 NT5E (0.62) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL3952851 0.88 AHCY (0.58) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL21562190 0.88 AHCY (0.58) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL3259052 0.88 AHCY (0.58) LMNANT5EHIF1AAHCYADORA2A
SCHEMBL29124737 0.88 NT5E (0.56) LMNANT5EHIF1AAHCYADORA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1898956-A4 ANTI-TUMORAL COMPOSITIONS AND METHODS UAB RESEARCH FOUNDATION (US) 2008-07-23 EP claimed
EP-1898956-A2 ANTI-TUMORAL COMPOSITIONS AND METHODS UAB Research Foundation (US) 2008-03-19 EP claimed
WO-2006124847-A2 ANTI-TUMORAL COMPOSITIONS AND METHODS UAB RESEARCH FOUNDATION (US) 2006-11-23 WO claimed
US-6177469-B1 ANTIUTOR AGENTS; AUTOIMMUNE DISEASES HEIDELBERG PHARMA HOLDING GMBH (DE) 2001-01-23 US claimed
CN-111909231-A 2 ' and/or 5 ' -amino acid ester phosphoramidate 3 ' -deoxyadenosine derivatives as anticancer compounds 努卡那有限公司 2020-11-10 CN disclosed
CN-107207554-B 2 ' and/or 5 ' -amino acid ester phosphoramidate 3 ' -deoxyadenosine derivatives as anticancer compounds 努卡那有限公司 2020-09-11 CN disclosed
EP-2331115-B3 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS UAB RES FOUND (US) 2018-12-05 EP disclosed
EP-3150220-A1 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS The UAB Research Foundation (US) 2017-04-05 EP disclosed
EP-2331115-B1 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS UAB RESEARCH FOUNDATION (US) 2016-10-05 EP disclosed
US-20160022784-A1 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS CORNELL UNIVERSITY 2016-01-28 US disclosed
US-20140199285-A1 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS SOUTHERN RESEARCH INSTITUTE (US) 2014-07-17 US disclosed
WO-2010019954-A9 PURINE NUCLEOSIDE PHOSPHORYLASE AS ENZYMATIC ACTIVATOR OF NUCLEOSIDE PRODRUGS THE UAB RESEARCH FOUNDATION (US) 2010-08-12 WO disclosed
US-7037718-B2 Mutant purine nucleoside phosphorylase proteins and cellular delivery thereof CORNELL RESEARCH FOUNDATION, INC. (US) 2006-05-02 US disclosed
US-20050214901-A1 Mutant purine nucleoside phosphorylase proteins and cellular delivery thereof CORNELL CENTER FOR TECHNOLOGY, ENTERPRISE & COIMMERCIALIZATION 2005-09-29 US disclosed
US-20030228576-A1 Nucleotide sequence coding for a cleaving enzyme; can use in conjuction with substrate to produce toxins which impair abnormal cell growth; antitumor agents NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2003-12-11 US disclosed
US-20030082167-A1 Lapid cleavage enzyme HEIDELBERG PHARMA HOLDING GMBH 2003-05-01 US disclosed
US-6521262-B2 Therapeutic active substances or active substance concentrates, in particular lipid conjugates of nucleosides which have gel-forming properties in aqueous media HEIDELBERG PHARMA HOLDING GMBH (DE) 2003-02-18 US disclosed
US-20020122817-A1 SOLID INSTANT-RELEASE FORMS OF ADMINISTRATION AND PROCESS FOR PRODUCING THE SAME HEIDELBERG PHARMA HOLDING GMBH (DE) 2002-09-05 US disclosed
US-20020106363-A1 LIPID CLEAVAGE ENZYME HEIDELBERG PHARMA HOLDING GMBH (DE) 2002-08-08 US disclosed
US-6177469-B1 ANTIUTOR AGENTS; AUTOIMMUNE DISEASES HEIDELBERG PHARMA HOLDING GMBH (DE) 2001-01-23 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 (4 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-20030082167-A1 Lapid cleavage enzyme LAP3, NAALAD2, ENGASE LMNA 235/4885NT5E 621/4885HIF1A 4012/4885
US-20050214901-A1 Mutant purine nucleoside phosphorylase proteins and cellular delivery thereof PNP, UPP1, TYMP LMNA 213/4885NT5E 44/4885HIF1A 4406/4885
US-20020122817-A1 SOLID INSTANT-RELEASE FORMS OF ADMINISTRATION AND PROCESS FOR PRODUCING THE SAME ADAR, PAICS, GART LMNA 1427/4885NT5E 119/4885HIF1A 4182/4885
US-20020106363-A1 LIPID CLEAVAGE ENZYME SMPD1, MMEL1, ENGASE LMNA 937/4885NT5E 528/4885HIF1A 4083/4885

“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.