SCHEMBL2476284

SCHEMBL2476284

O=C(c1ccc(Cl)cc1)C(O)[C@H]1OC(O)(Cl)C[C@@]1(O)C(=O)c1ccc(Cl)cc1

nearest known ligand 0.36

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 1/20 0.32
CES2 O00748 1/20 0.32
CES1 P23141 1/20 0.32
ALOX15 P16050 1/20 0.31
TSHR P16473 1/20 0.31
MEN1 O00255 2/20 0.31
KMT2A Q03164 2/20 0.31
GAA P10253 1/20 0.31
P2RX7 Q99572 2/20 0.30
CA1 P00915 1/20 0.30
CA2 P00918 1/20 0.30
ALDH1A1 P00352 1/20 0.30
PHGDH O43175 1/20 0.30
LMNA P02545 1/20 0.30

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
SCHEMBL2476289 1.00 GSK3B (0.32) GSK3BCES2CES1ALOX15TSHR
SCHEMBL8718920 0.90 HPGD (0.33) CES2CES1MEN1KMT2AGAA
SCHEMBL2471234 0.90 HPGD (0.33) CES2CES1MEN1KMT2AGAA
SCHEMBL6142770 0.90 HPGD (0.33) CES2CES1MEN1KMT2AGAA
SCHEMBL8112010 0.86 KMT2A (0.33) GSK3BCES2CES1MEN1KMT2A
SCHEMBL8112015 0.86 KMT2A (0.33) GSK3BCES2CES1MEN1KMT2A
SCHEMBL1799677 0.80 HPGD (0.33) CES2CES1MEN1KMT2AGAA
SCHEMBL8044926 0.78 P2RX7 (0.32) GSK3BCES2CES1ALOX15TSHR
SCHEMBL9594501 0.78 P2RX7 (0.32) GSK3BCES2CES1ALOX15TSHR
SCHEMBL11350296 0.78 P2RX7 (0.32) GSK3BCES2CES1ALOX15TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9266863-B2 Process for the synthesis of azacitidine and decitabine CHEMI SPA (IT) 2016-02-23 US claimed
EP-2371825-B1 Process for the synthesis of azacitidine and decitabine CHEMI SPA (IT) 2014-01-08 EP claimed
US-20110245485-A1 PROCESS FOR THE SYNTHESIS OF AZACITIDINE AND DECITABINE CHEMI SPA (IT) 2011-10-06 US claimed
EP-2371825-A1 Process for the synthesis of azacitidine and decitabine Chemi SPA (IT) 2011-10-05 EP claimed
US-9266863-B2 Process for the synthesis of azacitidine and decitabine CHEMI SPA (IT) 2016-02-23 US disclosed
EP-2371825-B1 Process for the synthesis of azacitidine and decitabine CHEMI SPA (IT) 2014-01-08 EP disclosed
US-20110245485-A1 PROCESS FOR THE SYNTHESIS OF AZACITIDINE AND DECITABINE CHEMI SPA (IT) 2011-10-06 US disclosed
EP-2371825-A1 Process for the synthesis of azacitidine and decitabine Chemi SPA (IT) 2011-10-05 EP disclosed
CN-101948493-A Industrial production method of high-purity decitabine JIANGSU AOSAIKANG PHARM CO LTD 2011-01-19 CN disclosed
JP-2000290289-A PRODUCTION OF 1-HALOGENO-2-DEOXYRIBOFURANOSE DERIVATIVE MITSUI CHEMICALS INC 2000-10-17 JP 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-20110245485-A1 PROCESS FOR THE SYNTHESIS OF AZACITIDINE AND DECITABINE DNMT1, TET1, TET2 GSK3B 1217/4885CES2 982/4885CES1 1620/4885

“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.