SCHEMBL2437269

SCHEMBL2437269

CC(=O)OCC(COCc1ccccc1)OCOCc1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.54
SLC1A1 P43005 1/20 0.43
CA1 P00915 4/20 0.42
CA2 P00918 2/20 0.42
CA7 P43166 2/20 0.42
CA9 Q16790 2/20 0.42
APOBEC3A P31941 1/20 0.40
APOBEC3G Q9HC16 1/20 0.40
TSHR P16473 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
TBXAS1 P24557 1/20 0.39
FOLH1 Q04609 1/20 0.39

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
SCHEMBL6378583 0.94 ALDH1A1 (0.54) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL3413225 0.91 ALDH1A1 (0.57) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL8196611 0.88 TDP1 (0.50) ALDH1A1SLC1A1SMN1; SMN2TBXAS1
SCHEMBL9191601 0.86 ALDH1A1 (0.51) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL9197596 0.86 ALDH1A1 (0.54) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL24827422 0.85 ALDH1A1 (0.57) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL9019803 0.85 ALDH1A1 (0.50) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL21344787 0.85 ALDH1A1 (0.65) ALDH1A1SLC1A1
SCHEMBL9019848 0.84 ALDH1A1 (0.47) ALDH1A1SLC1A1CA1CA2CA7
SCHEMBL14125262 0.83 ALDH1A1 (0.51) ALDH1A1SLC1A1CA1CA2CA7

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0806425-B1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LAB LTD (IN) 2001-08-29 EP claimed
US-5821367-A REACTING A DIACYLGUANINE AND AN ALKYLATING AGENT IN THE ABSENCE OF AN ACID CATALYST AND A SOLVENT LUPIN LABORATORIES LIMITED (IN) 1998-10-13 US claimed
EP-0806425-A1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 1997-11-12 EP claimed
WO-2011114336-A1 PROCESS FOR THE ISOLATION OF GANCICLOVIR INTERMEDIATE HETERO RESEARCH FOUNDATION (IN) 2011-09-22 WO disclosed
US-7078524-B2 Process for the synthesis of ganciclovir RANBAXY LABORATORIES LIMITED (US) 2006-07-18 US disclosed
US-20050176956-A1 Process for the preparation of ganciclovir intermediate n2-acetyl-9-(1,3-diacetoxy-2-propoxymethyl) guanine RANBAXY LABORATORIES LIMITED (IN) 2005-08-11 US disclosed
US-20040102628-A1 Process for the synthesis of ganciclovir RANBAXY LABORATORIES LIMITED (IN) 2004-05-27 US disclosed
EP-0806425-B1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LAB LTD (IN) 2001-08-29 EP disclosed
US-6043364-A HEATING THE ISOMER IN AN ALKYLATING AGENT IN ABSENCE OF ACID CATALYST AND SOLVENT LUPIN LABORATORIES LIMITED (IN) 2000-03-28 US disclosed
EP-0976751-A1 A process for the isomerisation of an N-7 isomer into an N-9 isomer useful in the synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 2000-02-02 EP disclosed
US-5821367-A REACTING A DIACYLGUANINE AND AN ALKYLATING AGENT IN THE ABSENCE OF AN ACID CATALYST AND A SOLVENT LUPIN LABORATORIES LIMITED (IN) 1998-10-13 US disclosed
US-5821367-A REACTING A DIACYLGUANINE AND AN ALKYLATING AGENT IN THE ABSENCE OF AN ACID CATALYST AND A SOLVENT LUPIN LABORATORIES LIMITED (IN) 1998-10-13 US disclosed
EP-0806425-A1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 1997-11-12 EP disclosed
EP-0806425-A1 An improved regiospecific process for synthesis of acyclic nucleosides LUPIN LABORATORIES LIMITED (IN) 1997-11-12 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-20040102628-A1 Process for the synthesis of ganciclovir TYMP, MTAP, TPMT ALDH1A1 2906/4885SLC1A1 3371/4885CA1 3583/4885
US-20050176956-A1 Process for the preparation of ganciclovir intermediate n2-acetyl-9-(1,3-diacetoxy-2-propoxymethyl) guanine GNE, MPG, B3GNT2 ALDH1A1 1675/4885SLC1A1 3668/4885CA1 3206/4885

“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.