Purine

Purine

SCHEMBL595231

O=P(O)(O)O.O=P(O)(O)O.O=P(O)(O)O.c1ncc2[nH]cnc2n1

nearest known ligand 0.39

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Purine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.39
KDM4E B2RXH2 1/20 0.39
RXFP1 Q9HBX9 1/20 0.38
FDPS P14324 2/20 0.33
PI4KA P42356 2/20 0.32
PI4K2B Q8TCG2 2/20 0.32
PI4K2A Q9BTU6 2/20 0.32
PI4KB Q9UBF8 2/20 0.32
LRRK2 Q5S007 2/20 0.32
LMNA P02545 1/20 0.32
DRD3 P35462 1/20 0.32
XDH P47989 1/20 0.32
NTRK1 P04629 1/20 0.32
ENPP1 P22413 1/20 0.32
BRD4 O60885 1/20 0.32
CDK2 P24941 2/20 0.32
G6PD P11413 1/20 0.32
METAP2 P50579 1/20 0.31
METAP1 P53582 1/20 0.31
PAK1 Q13153 1/20 0.30

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
Purine SCHEMBL5989434 1.00 ALDH1A1 (0.39) ALDH1A1KDM4ERXFP1FDPSPI4KA
Purine SCHEMBL27554272 1.00 ALDH1A1 (0.39) ALDH1A1KDM4ERXFP1FDPSPI4KA
Purine SCHEMBL2676962 0.93 ALDH1A1 (0.41) ALDH1A1KDM4ERXFP1FDPSPI4KA
Purine SCHEMBL7453138 0.91 ALDH1A1 (0.33) ALDH1A1KDM4ERXFP1
Purine SCHEMBL7453075 0.91 ALDH1A1 (0.33) ALDH1A1KDM4ERXFP1
Pyrophosphoric Acid SCHEMBL637333 0.90 ALDH1A1 (0.35) ALDH1A1KDM4ERXFP1FDPSNTRK1
Purine SCHEMBL28271 0.89 ALDH1A1 (0.39) ALDH1A1KDM4ERXFP1PI4KAPI4K2B
Purine SCHEMBL28164598 0.88 ALDH1A1 (0.44) ALDH1A1KDM4ERXFP1PI4KAPI4K2B
Purine SCHEMBL2120554 0.88 ALDH1A1 (0.47) ALDH1A1KDM4ERXFP1PI4KAPI4K2B
Purine SCHEMBL3158 0.88

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2812441-A1 NUCLEIC ACID LIGATION METHOD Wisconsin Alumni Research Foundation (US) 2014-12-17 EP claimed
WO-2013119690-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2013-08-15 WO claimed
US-20130203635-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION 2013-08-08 US claimed
CN-108472371-B EGFR antibody-drug conjugate and application thereof in medicine 江苏恒瑞医药股份有限公司 2022-05-24 CN disclosed
US-8981078-B2 Selective inhibitors of translesion DNA replication CASE WESTERN RESERVE UNIVERSITY (US) 2015-03-17 US disclosed
EP-2812441-A1 NUCLEIC ACID LIGATION METHOD Wisconsin Alumni Research Foundation (US) 2014-12-17 EP disclosed
EP-2812441-A1 NUCLEIC ACID LIGATION METHOD Wisconsin Alumni Research Foundation (US) 2014-12-17 EP disclosed
WO-2013119690-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2013-08-15 WO disclosed
WO-2013119690-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 2013-08-15 WO disclosed
US-20130203635-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION 2013-08-08 US disclosed
US-20130203635-A1 NUCLEIC ACID LIGATION METHOD WISCONSIN ALUMNI RESEARCH FOUNDATION 2013-08-08 US disclosed
US-20130004945-A1 SELECTIVE INHIBITORS OF TRANSLESION DNA REPLICATION BERDIS ANTHONY J (US) 2013-01-03 US disclosed
US-8114847-B2 Selective inhibitors of translesion DNA replication CASE WESTERN RESERVE UNIVERSITY (US) 2012-02-14 US disclosed
US-20090048202-A1 SELECTIVE INHIBITORS OF TRANSLESION DNA REPLICATION CASE WESTERN RESERVE UNIVERSITY 2009-02-19 US disclosed
WO-2006101911-A1 SELECTIVE INHIBITORS OF TRANSLESION DNA REPLICATION CASE WESTERN RESERVE UNIVERSITY (US) 2006-09-28 WO disclosed
US-20030180396-A1 Method of effecting phosphorylation in eucaryotic cells using thiamine triphosphate INSTITUT PASTEUR (FR) 2003-09-25 US disclosed
EP-1229919-A2 A METHOD OF EFFECTING PHOSPHORYLATION IN EUCARYOTIC CELLS USING THIAMINE TRIPHOSPHATE INSTITUT PASTEUR (FR) 2002-08-14 EP disclosed
US-6380169-B1 FOR INHIBITING MESSENGER RNA TRANSLATION USING ANTI-SENSE OLIGONUCLEOSIDES CONTAINING 5'-CAP CLEAVAGE MOIETIES ISIS PHARMACEUTICALS, INC. 2002-04-30 US disclosed
WO-2001010444-A2 A METHOD OF EFFECTING PHOSPHORYLATION IN EUCARYOTIC CELLS USING THIAMINE TRIPHOSPHATE INSTITUT PASTEUR (FR) 2001-02-15 WO disclosed
WO-1996006621-A1 METAL COMPLEX CONTAINING OLIGONUCLEOSIDE CLEAVAGE COMPOUNDS AND THERAPIES GENTA INCORPORATED (US) 1996-03-07 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-20090048202-A1 SELECTIVE INHIBITORS OF TRANSLESION DNA REPLICATION REV1, PCNA, DNA2 ALDH1A1 3867/4885KDM4E 1700/4885RXFP1 4576/4885

“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.