SCHEMBL170695

SCHEMBL170695

C=CCn1cnc(N)c2ncnc1-2

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADORA2A P29274 4/20 0.41
ADORA2B P29275 2/20 0.37
ADORA1 P30542 2/20 0.37
ADORA3 P0DMS8 1/20 0.37
NPC1 O15118 1/20 0.35
HPGD P15428 1/20 0.35
RAB9A P51151 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
JAK2 O60674 1/20 0.35
AHCY P23526 6/20 0.34
PI4KA P42356 1/20 0.33
PI4K2B Q8TCG2 1/20 0.33
PI4K2A Q9BTU6 1/20 0.33
PI4KB Q9UBF8 1/20 0.33
PIK3CD O00329 1/20 0.32
PIK3CA P42336 1/20 0.32
PIK3CB P42338 1/20 0.32
PIK3CG P48736 1/20 0.32
PRKDC P78527 1/20 0.32
SLC2A1 P11166 1/20 0.32

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
SCHEMBL11076308 0.80 AHCY (0.57) ADORA2AADORA2BADORA1JAK2AHCY
SCHEMBL9108201 0.79 ADORA2A (0.36) ADORA2AADORA2BADORA1SMN1; SMN2AHCY
3-Ethyladenine SCHEMBL48200 0.77 ADORA2A (0.50) ADORA2AADORA2BADORA1ADORA3SMN1; SMN2
SCHEMBL5513295 0.77 ADORA2A (0.35) ADORA2AADORA2BADORA1SMN1; SMN2AHCY
3-Propyladenine SCHEMBL15756434 0.75 ADORA2A (0.53) ADORA2AADORA2BADORA1ADORA3SMN1; SMN2
3-Benzyladenine SCHEMBL5352368 0.71 ADORA2A (0.56) ADORA2ASMN1; SMN2PI4KAPI4K2BPI4K2A
SCHEMBL1882911 0.71
SCHEMBL1798270 0.70 ADORA2A (0.72) ADORA2AADORA2BADORA1AHCYPI4KA
SCHEMBL9778803 0.70 ADORA2A (0.63) ADORA2AADORA2BADORA1ADORA3AHCY
SCHEMBL21121959 0.70 KCNH2 (0.44) ADORA2ASMN1; SMN2JAK2PI4KAPI4K2B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240175010-A1 Methods of Library Preparation ILLUMINA, INC. (US) 2024-05-30 US claimed
WO-2024059788-A2 METHOD, KIT AND SYSTEM FOR END LABELING OF NUCLEIC ACIDS Chen cheng yao 2024-03-21 WO claimed
CN-117651767-A Improved methods for isothermal complementary DNA and library preparation ILLUMINA公司 2024-03-05 CN claimed
EP-4314279-A1 IMPROVED METHODS OF LIBRARY PREPARATION Illumina, Inc. (US) 2024-02-07 EP claimed
EP-4314282-A1 IMPROVED METHODS OF ISOTHERMAL COMPLEMENTARY DNA AND LIBRARY PREPARATION Illumina, Inc. (US) 2024-02-07 EP claimed
CN-117062910-A Improved library preparation method ILLUMINA公司 2023-11-14 CN claimed
US-20240209396-A1 SMALL CAS PROTEINS AND USES THEREOF HUIDAGENE THERAPEUTICS CO., LTD. (CN) 2024-06-27 US disclosed
CN-111278974-B Hook probe, nucleic acid ligation method, and method for constructing sequencing library 深圳华大智造科技股份有限公司 2024-06-11 CN disclosed
US-20240175010-A1 Methods of Library Preparation ILLUMINA, INC. (US) 2024-05-30 US disclosed
US-20240150753-A1 METHODS OF ISOTHERMAL COMPLEMENTARY DNA AND LIBRARY PREPARATION ILLUMINA, INC. (US) 2024-05-09 US disclosed
WO-2024059788-A2 METHOD, KIT AND SYSTEM FOR END LABELING OF NUCLEIC ACIDS Chen cheng yao 2024-03-21 WO disclosed
US-20240076651-A1 SYSTEMS, METHODS, AND COMPOSITIONS FOR TARGETED NUCLEIC ACID EDITING NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2024-03-07 US disclosed
CN-117651767-A Improved methods for isothermal complementary DNA and library preparation ILLUMINA公司 2024-03-05 CN disclosed
US-6046036-A FOR INCREASING SURVIVAL RATE OF NON-TARGET CELLS SUCH AS HEMATOPOIETIC CELLS WHEN CONTACTED WITH ANTICARCINOGENIC/DNA-DAMAGING AGENTS DURING MULTIAGENT CHEMOTHERAPY PROTOCOLS OR IN FANCONI'S ANEMIA ADVANCED RESEARCH AND TECHNOLOGY INSTITUTE (US) 2000-04-04 US disclosed
WO-1998017684-A2 DNA SEQUENCES ENCODING FUSIONS OF DNA REPAIR PROTEINS AND USES THEREOF ADVANCED RESEARCH & TECHNOLOGY INSTITUTE (US) 1998-04-30 WO disclosed
EP-0651825-B1 METHODS AND DIAGNOSTIC KITS FOR DETERMINING THE TOXICITY OF A COMPOUND UTILIZING BACTERIAL STRESS PROMOTERS FUSED TO REPORTER GENES HARVARD COLLEGE (US) 1998-01-14 EP disclosed
US-5589337-A Methods and diagnostic kits for determining toxicity utilizing bacterial stress promoters fused to reporter genes THE PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1996-12-31 US disclosed
US-5585232-A Methods and diagnostic kits for determining toxicity utilizing E. coli stress promoters fused to reporter genes PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1996-12-17 US disclosed
EP-0651825-A1 METHODS AND DIAGNOSTIC KITS FOR DETERMINING THE TOXICITY OF A COMPOUND UTILIZING BACTERIAL STRESS PROMOTERS FUSED TO REPORTER GENES PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1995-05-10 EP disclosed
WO-1994001584-A1 METHODS AND DIAGNOSTIC KITS FOR DETERMINING TOXICITY UTILIZING BACTERIAL STRESS PROMOTERS FUSED TO REPORTER GENES PRESIDENT AND FELLOWS OF HARVARD COLLEGE (US) 1994-01-20 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-20240076651-A1 SYSTEMS, METHODS, AND COMPOSITIONS FOR TARGETED NUCLEIC ACID EDITING ADA, APOBEC3A, CDA ADORA2A 360/4885ADORA2B 933/4885ADORA1 526/4885

“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.