SCHEMBL532653

SCHEMBL532653

C=CCc1ncnc2nc[nH]c12

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HIF1A Q16665 2/20 0.49
PI4KA P42356 2/20 0.47
PI4K2B Q8TCG2 2/20 0.47
PI4K2A Q9BTU6 2/20 0.47
PI4KB Q9UBF8 2/20 0.47
LRRK2 Q5S007 2/20 0.47
LMNA P02545 2/20 0.47
DRD3 P35462 1/20 0.47
XDH P47989 1/20 0.47
G6PD P11413 1/20 0.46
PDPK1 O15530 2/20 0.43
CDK2 P24941 2/20 0.43
TP53 P04637 2/20 0.43
HSD17B10 Q99714 2/20 0.43
CHEK1 O14757 1/20 0.43
AURKA O14965 1/20 0.43
CHEK2 O96017 1/20 0.43
HSP90AA1 P07900 1/20 0.43
HSP90AB1 P08238 1/20 0.43
PRKACA P17612 1/20 0.43

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
SCHEMBL6749169 0.82 PI4KA (0.47) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL5433393 0.79 PI4KA (0.44) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL3313639 0.76 PI4KA (0.57) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL3661701 0.76 PI4KA (0.57) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL11903083 0.76 CYP3A4 (0.53) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL2930055 0.76 HSD17B10 (0.56) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL10435360 0.75 CDK2 (0.42) HIF1AXDHPDPK1CDK2MAP3K5
SCHEMBL7194482 0.74 HIF1A (0.30) HIF1A
SCHEMBL10597139 0.73 HSD17B10 (0.40) HIF1API4KAPI4K2BPI4K2API4KB
SCHEMBL6270509 0.72 CDK2 (0.61) HIF1API4KAPI4K2BPI4K2API4KB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117659015-A Synthesis method for promoting 6-alkyl purine nucleoside by using water system illumination 新乡学院 2024-03-08 CN claimed
EP-2322518-B1 Method of manufacture of 1,3-dioxolane and 1,3-oxathiolane nucleosides GILEAD SCIENCES INC (US) 2015-02-25 EP claimed
US-20140121186-A1 Compounds, Compositions and Methods for Treating Ocular Conditions CHIMERIX, INC. (US) 2014-05-01 US claimed
WO-2011011519-A1 COMPOUNDS, COMPOSITIONS AND METHODS FOR TREATING OCULAR CONDITIONS CHIMERIX, INC. (US) 2011-01-27 WO claimed
US-6939965-B2 Process of manufacture of 1,3-oxathiolane nucleosides using titanium trichloride mono-isopropoxide GILEAD SCIENCES, INC. (US) 2005-09-06 US claimed
US-6518425-B1 A process for producing a 1,3-oxathiolane nucleoside comprising reacting a 5-halo-2-protected-oxymethyl-1,3-oxathiolane with a silylated purine or pyrimidine without the addition of a Lewis acid or an additional base to the reaction EMORY UNIVERSITY 2003-02-11 US claimed
US-20030013880-A1 Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers APOTEX PHARMACHEM INC (CA) 2003-01-16 US claimed
CN-119119156-A Bridged artificial nucleic acid ALNA 田边三菱制药株式会社 2024-12-13 CN disclosed
CN-112996522-B Bridged artificial nucleic acid ALNA 田边三菱制药株式会社 2024-09-20 CN disclosed
CN-117964673-A Bridged artificial nucleic acid ALNA 田边三菱制药株式会社 2024-05-03 CN disclosed
CN-117964674-A Bridged artificial nucleic acid ALNA 田边三菱制药株式会社 2024-05-03 CN disclosed
EP-2697242-B1 2'-AZIDO SUBSTITUTED NUCLEOSIDE DERIVATIVES AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES MERCK SHARP & DOHME (US) 2018-10-03 EP disclosed
EP-2696681-B1 2'-SUBSTITUTED NUCLEOSIDE DERIVATIVES AND METHODS OF USE THEREOF FOR THE TREATMENT OF VIRAL DISEASES MERCK SHARP & DOHME (US) 2018-10-03 EP disclosed
WO-2000009531-A2 β-L-2'-DEOXY-NUCLEOSIDES FOR THE TREATMENT OF HEPATITIS B NOVIRIO PHARMACEUTICALS LIMITED (KY) 2000-02-24 WO disclosed
WO-2000009494-A1 METHOD OF MANUFACTURE OF 1,3-OXATHIOLANE NUCLEOSIDES TRIANGLE PHARMACEUTICALS, INC. (US) 2000-02-24 WO disclosed
US-5869467-A VIRICIDES INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY OF THE ACADEMY OF SCIENCES OF THE CZECH REPUBLIC (CZ) 1999-02-09 US disclosed
US-5641763-A N-phosphonylmethoxyalkyl derivatives of pyrimdine and purine bases and a therapeutical composition therefrom with antiviral activity INSTITUTE OF ORGANIC CHEMISTRY AND BIOCHEMISTRY OF THE ACADEMY OF SCIENCES OF THE CZECH REPUBLIC (CZ) 1997-06-24 US disclosed
US-5142051-A Viricides special for mutants of herpes viruses CESKOSLOVENSKA AKADEMIE VED (CS) 1992-08-25 US disclosed
EP-0253412-B1 N-PHOSPHONYLMETHOXYALKYL DERIVATIVES OF PYRIMIDINE AND PURINE BASES, METHODS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THEREFROM WITH ANTIVIRAL ACTIVITY Ceskoslovenska akademie ved (CS) 1990-10-31 EP disclosed
EP-0253412-A2 N-Phosphonylmethoxyalkyl derivatives of pyrimidine and purine bases, methods for their preparation and pharmaceutical compositions therefrom with antiviral activity Ceskoslovenska akademie ved (CS) 1988-01-20 EP 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-20140121186-A1 Compounds, Compositions and Methods for Treating Ocular Conditions EYA3, EYA2, PDE6C HIF1A 685/4885PI4KA 2898/4885PI4K2B 2779/4885
US-20030013880-A1 Process for recovery of the desired cis-1,3-oxathiolane nucleosides from their undesired trans-isomers SLC29A1, NUDT1, SLC28A1 HIF1A 3969/4885PI4KA 2155/4885PI4K2B 2930/4885

“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.