SCHEMBL1826964

SCHEMBL1826964

O=C(OC[C@H]1OC(n2ccc(=O)nc2)[C@H](OC(=O)c2ccccc2)[C@@H]1OC(=O)c1ccccc1)c1ccccc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ POLB P06746 2/20 0.60
▸ MEN1 O00255 1/20 0.60
▸ USP2 O75604 1/20 0.60
▸ KMT2A Q03164 1/20 0.60
▸ ALDH1A1 P00352 3/20 0.50
▸ CA1 P00915 2/20 0.50
▸ CA2 P00918 2/20 0.50
▸ CA9 Q16790 2/20 0.50
▸ GAPDH P04406 2/20 0.47
▸ HRAS P01112 1/20 0.45
▸ P2RX3 P56373 1/20 0.43
▸ P2RX4 Q99571 1/20 0.43
▸ P2RX2 Q9UBL9 1/20 0.43
▸ HTT P42858 1/20 0.41
▸ PTPN1 P18031 1/20 0.41
▸ TSHR P16473 1/20 0.41
▸ LMNA P02545 2/20 0.40
▸ THRB P10828 1/20 0.40
▸ SMN1; SMN2 Q16637 1/20 0.40
▸ HIF1A Q16665 1/20 0.40

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
SCHEMBL1826966 1.00 POLB (0.60) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL10244723 0.93 ALDH1A1 (0.52) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL14570583 0.93 ALDH1A1 (0.52) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL17612287 0.92 POLB (0.54) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL11442315 0.85 USP2 (0.62) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL10260643 0.81 MEN1 (0.58) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL15702572 0.81 MEN1 (0.58) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL7706306 0.81 POLB (0.58) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL10706978 0.81 MEN1 (0.56) POLBMEN1USP2KMT2AALDH1A1
SCHEMBL7712704 0.81 MEN1 (0.58) POLBMEN1USP2KMT2AALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2319853-B1 Process for the production of 2'-branched nucleosides IDENIX PHARMACEUTICALS INC (US) 2014-03-12 — — EP disclosed
EP-2319853-A1 Process for the production of 2'-branched nucleosides Idenix (Cayman) Limited (KY) 2011-05-11 — — EP disclosed
US-7598373-B2 Process for the production of 2-C-methyl-D-ribonolactone IDENIX PHARMACEUTICALS, INC. (US) 2009-10-06 — — US disclosed
US-7582748-B2 efficient synthetic route to an optionally protected 1-halo-2-deoxyribose; formation of an alkyl acetal, such as a methyl acetal, of a furanose, such as 2-deoxyribose, optionally protecting the remaining hydroxyl groups of the furanose, reacting the acetal with an acyl halide that forms the acid halide MICROBIOLOGICA QUIMICA E FARMACEUTICAL LTD. (BR) 2009-09-01 — — US disclosed
EP-1585529-A4 PROCESS FOR THE PRODUCTION OF 2'-BRANCHED NUCLEOSIDES IDENIX CAYMAN LTD (KY) 2008-05-28 — — EP disclosed
EP-1575971-A4 PROCESS FOR THE PRODUCTION OF 3 -NUCLEOSIDE PRODRUGS IDENIX CAYMAN LTD (KY) 2008-03-05 — — EP disclosed
EP-1745573-A2 METHODS OF MANUFACTURE OF 2 -DEOXY-&bgr;-L-NUCLEOSIDES Microbiologica Quimica E Farmaceutica Ltd. (BR) 2007-01-24 — — EP disclosed
EP-1585529-A2 PROCESS FOR THE PRODUCTION OF 2'-BRANCHED NUCLEOSIDES Idenix (Cayman) Limited (KY) 2005-10-19 — — EP disclosed
EP-1575971-A1 PROCESS FOR THE PRODUCTION OF 3 -NUCLEOSIDE PRODRUGS Idenix (Cayman) Limited (KY) 2005-09-21 — — EP disclosed
US-20050020825-A1 Process for the production of 2'-branched nucleosides IDENIX PHARMACEUTICALS LLC 2005-01-27 — — US disclosed
US-20040266996-A1 Methods of manufacture of 2'-deoxy-beta-L-nucleosides MICROBIOLOGICA QUIMICA E FARMACEUTICA LTD. (BR) 2004-12-30 — — US disclosed
WO-2004084453-A2 METHODS OF MANUFACTURE OF 2'-DEOXY-β-L-NUCLEOSIDES MICROBIOLOGICA QUIMICA E FARMACEUTICA LTD. (BR) 2004-09-30 — — WO disclosed
US-20040181051-A1 Process for the production of 3'-nucleoside prodrugs STORER RICHARD (GB) 2004-09-16 — — US disclosed
WO-2004058792-A1 PROCESS FOR THE PRODUCTION OF 3'-NUCLEOSIDE PRODRUGS IDENIX (CAYMAN) LIMITED (KY) 2004-07-15 — — WO disclosed
WO-2004052899-A2 PROCESS FOR THE PRODUCTION OF 2'-BRANCHED NUCLEOSIDES IDENIX (CAYMAN) LIMITED (KY) 2004-06-24 — — 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 (3 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-20040266996-A1 Methods of manufacture of 2'-deoxy-beta-L-nucleosides DUT, DAO, DCTD POLB 216/4885MEN1 3439/4885USP2 2267/4885
US-20040181051-A1 Process for the production of 3'-nucleoside prodrugs PNP, GART, UMPS POLB 853/4885MEN1 4748/4885USP2 4137/4885
US-20050020825-A1 Process for the production of 2'-branched nucleosides RNGTT, MTAP, NSUN2 POLB 68/4885MEN1 3011/4885USP2 3883/4885

“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.

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