SCHEMBL2471234

SCHEMBL2471234

Cc1ccc(C(=O)C(O)[C@H]2OC(O)(Cl)C[C@@]2(O)C(=O)c2ccc(C)cc2)cc1

nearest known ligand 0.33

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HPGD P15428 3/20 0.33
CES2 O00748 2/20 0.33
CES1 P23141 2/20 0.33
NPC1 O15118 2/20 0.31
RAB9A P51151 2/20 0.31
L3MBTL1 Q9Y468 1/20 0.31
CHRM2 P08172 1/20 0.31
ADRA2B P18089 1/20 0.31
DRD3 P35462 1/20 0.31
SIGMAR1 Q99720 1/20 0.31
HRH3 Q9Y5N1 1/20 0.31
SMN1; SMN2 Q16637 2/20 0.31
PKM P14618 1/20 0.31
CYP1A2 P05177 1/20 0.31
CYP2C19 P33261 1/20 0.31
TDP1 Q9NUW8 1/20 0.30
SLC6A3 Q01959 4/20 0.30
SLC6A2 P23975 3/20 0.30
SLC6A4 P31645 3/20 0.30
LMNA P02545 3/20 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
SCHEMBL6142770 1.00 HPGD (0.33) HPGDCES2CES1NPC1RAB9A
SCHEMBL8718920 1.00 HPGD (0.33) HPGDCES2CES1NPC1RAB9A
SCHEMBL1799677 0.90 HPGD (0.33) HPGDCES2CES1NPC1RAB9A
SCHEMBL2476284 0.90 GSK3B (0.32) CES2CES1LMNAALDH1A1GAA
SCHEMBL2476289 0.90 GSK3B (0.32) CES2CES1LMNAALDH1A1GAA
SCHEMBL8112010 0.79 KMT2A (0.33) HPGDCES2CES1L3MBTL1LMNA
SCHEMBL8112015 0.79 KMT2A (0.33) HPGDCES2CES1L3MBTL1LMNA
SCHEMBL9614440 0.78 HPGD (0.33) HPGDCES2CES1CHRM2ADRA2B
SCHEMBL11104413 0.78 HPGD (0.33) HPGDCES2CES1CHRM2ADRA2B
SCHEMBL16446965 0.78 HPGD (0.33) HPGDCES2CES1CHRM2ADRA2B

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
EP-0548798-A1 Antiviral agent SANWA KAGAKU KENKYUSHO CO., LTD. (JP) 1993-06-30 EP disclosed
US-4663446-A BACTERICIDES, POLYMERASE INHIBITORS TRUSTEES OF THE UNIV. OF MASSACHUSETTS (US) 1987-05-05 US 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 HPGD 2808/4885CES2 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.