SCHEMBL1009012

SCHEMBL1009012

O=c1nc(Cl)[nH]c2nc[nH]c12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE P22303 1/20 0.50
GDA Q9Y2T3 1/20 0.50
ABL1 P00519 1/20 0.46
RIN1 Q13671 1/20 0.46
ADORA2B P29275 6/20 0.44
ADORA2A P29274 4/20 0.44
ADORA3 P0DMS8 6/20 0.42
ALDH1A1 P00352 2/20 0.42
USP2 O75604 1/20 0.42
TP53 P04637 1/20 0.42
HPGD P15428 1/20 0.42
PTGS1 P23219 1/20 0.42
MAPK3 P27361 1/20 0.42
XDH P47989 1/20 0.42
HBB P68871 1/20 0.42
PAX8 Q06710 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
TDP1 Q9NUW8 1/20 0.41
PDE4A P27815 3/20 0.41
PDE4B Q07343 3/20 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
Hydrochloric Acid SCHEMBL9666845 0.98 ACHE (0.48) ACHEGDAABL1RIN1ADORA2B
Water SCHEMBL9462016 0.98 ACHE (0.48) ACHEGDAABL1RIN1ADORA2B
Hydrochloric Acid SCHEMBL9461578 0.96 ACHE (0.47) ACHEGDAABL1RIN1ADORA2B
Water SCHEMBL9461623 0.96 ACHE (0.47) ACHEGDAABL1RIN1ADORA2B
SCHEMBL1898184 0.78 GDA (0.48) ACHEGDAABL1RIN1ADORA2B
Guanine SCHEMBL342789 0.78 ADORA3 (0.62) ACHEGDAABL1RIN1ADORA2B
SCHEMBL6429381 0.78 GDA (0.48) ACHEGDAABL1RIN1ADORA2B
SCHEMBL8230116 0.78 ACHE (0.48) ACHEGDAABL1RIN1ADORA2B
SCHEMBL612212 0.78 ACHE (0.48) ACHEGDAABL1RIN1ADORA2B
SCHEMBL8663355 0.76 GDA (0.46) ACHEGDAABL1RIN1ADORA2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0466164-B1 Process for the preparation of 2-chloro-1,7-dihydropurin-6-one and process for the purification of the same BOEHRINGER INGELHEIM KG (DE) 1995-06-07 EP claimed
US-5264573-A Process for preparing 2-chloro-1,7-dihydropurin-6-one and a process for its purification BOEHRINGER INGELHEIM GMBH (DE) 1993-11-23 US claimed
JP-4230383-A None JP disclosed
CN-121721172-A Solid phase extraction-vacuum centrifugal concentration-liquid chromatography tandem mass spectrometry detection method for chloro-product of flavor nucleotide 浙江大学 2026-03-24 CN disclosed
EP-2268607-B9 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID CTI BIO (KR) 2015-05-13 EP disclosed
EP-2268607-B1 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID CTI BIO (KR) 2015-02-18 EP disclosed
US-8895734-B2 Peptide nucleic acid derivatives with good cell penetration and strong affinity for nucleic acid OLIPASS CORPORATION (KR) 2014-11-25 US disclosed
US-8884008-B2 Peptide nucleic acid derivatives with good cell penetration and strong affinity for nucleic acid OLIPASS CORPORATION (KR) 2014-11-11 US disclosed
US-20140323728-A1 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID CTI BIO (KR) 2014-10-30 US disclosed
US-8859766-B2 Peptide nucleic acid derivatives with good cell penetration and strong affinity for nucleic acid OLIPASS CORPORATION (KR) 2014-10-14 US disclosed
US-20140155605-A1 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID CTI BIO (KR) 2014-06-05 US disclosed
WO-2009113828-A2 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID CTI BIO (KR) 2009-09-17 WO disclosed
US-5658731-A GENE EXPRESSION; COMPLEXING REACTIONS EUROPAISCHES LABORATORIUM FUR MOLEKULARBIOLOGIE (DE) 1997-08-19 US disclosed
US-5264573-A Process for preparing 2-chloro-1,7-dihydropurin-6-one and a process for its purification BOEHRINGER INGELHEIM GMBH (DE) 1993-11-23 US disclosed
JP-H04230383-A PRODUCTION OF 2-CHLORO-1,7-DIHYDRO PURIN-6-ONE, AND ITS PURIFICATION BOEHRINGER INGELHEIM KG 1992-08-19 JP disclosed
US-4663446-A BACTERICIDES, POLYMERASE INHIBITORS TRUSTEES OF THE UNIV. OF MASSACHUSETTS (US) 1987-05-05 US disclosed
US-4602089-A Process for preparing purine compounds NEWPORT PHARMACEUTICALS, INC. (US) 1986-07-22 US disclosed
EP-0126813-A1 Process for preparing imidazole compounds Newport Pharmaceuticals International, Inc. (US) 1984-12-05 EP disclosed
US-4451478-A IMMUNOLOGY, ACTIVATORS NEWPORT PHARMACEUTICALS INTERNATIONAL, INC. (US) 1984-05-29 US disclosed
US-4371613-A TRANSARABINOSYLATION USING AN ENZYME FROM BACTERIA, AN ARABINOSE DONOR AND A PURINE SOURCE AJINOMOTO COMPANY INCORPORATED (JP) 1983-02-01 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 (2 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-20140323728-A1 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID SLC7A1, SLC29A1, SLC43A3 ACHE 4861/4885GDA 508/4885ABL1 2910/4885
US-20140155605-A1 PEPTIDE NUCLEIC ACID DERIVATIVES WITH GOOD CELL PENETRATION AND STRONG AFFINITY FOR NUCLEIC ACID SLC7A1, SLC29A1, SLC43A3 ACHE 4861/4885GDA 508/4885ABL1 2910/4885

“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.