SCHEMBL17090840

SCHEMBL17090840

COc1ccc(C(OC[C@H]2O[C@@H](n3ccc(NC(=O)c4ccccc4)nc3=O)C[C@@H]2OC(=O)CCC(C)=O)(c2ccccc2)c2ccc(OC)cc2)cc1

nearest known ligand 0.57

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.57
ABL1 P00519 1/20 0.45
RIN1 Q13671 1/20 0.45
P2RY6 Q15077 3/20 0.40
P2RY14 Q15391 2/20 0.40
NT5E P21589 2/20 0.40
TYMP P19971 4/20 0.38
ADORA3 P0DMS8 2/20 0.35
RNASE1 P07998 1/20 0.33
F2 P00734 1/20 0.33
P2RY2 P41231 1/20 0.32
P2RY4 P51582 1/20 0.32
SLC6A1 P30531 2/20 0.32
SLC6A11 P48066 1/20 0.32

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
SCHEMBL17223096 1.00 POLB (0.57) POLBABL1RIN1P2RY6P2RY14
SCHEMBL17223098 1.00 POLB (0.57) POLBABL1RIN1P2RY6P2RY14
SCHEMBL14049948 0.95 POLB (0.58) POLBABL1RIN1P2RY6P2RY14
SCHEMBL12724655 0.89 POLB (0.46) POLBABL1RIN1P2RY6P2RY14
SCHEMBL13897164 0.89 POLB (0.46) POLBABL1RIN1P2RY6P2RY14
SCHEMBL6932396 0.89 POLB (0.59) POLBABL1RIN1P2RY6P2RY14
SCHEMBL17992980 0.88 POLB (0.59) POLBABL1RIN1P2RY6P2RY14
SCHEMBL12724971 0.87 POLB (0.46) POLBABL1RIN1P2RY6P2RY14
SCHEMBL13897166 0.87 POLB (0.46) POLBABL1RIN1P2RY6P2RY14
SCHEMBL23157266 0.86 POLB (0.56) POLBABL1RIN1P2RY6P2RY14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2020-08-04 US disclosed
EP-2921499-B1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACIDS TAKEDA PHARMACEUTICALS CO (JP) 2020-01-22 EP disclosed
US-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2019-05-09 US disclosed
US-20150315229-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2015-11-05 US disclosed
EP-2921499-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID Takeda Pharmaceutical Company Limited (JP) 2015-09-23 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 (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-20150315229-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID POLM, POLRMT, RNMT POLB 15/4885ABL1 2284/4885RIN1 2508/4885
US-20190135852-A1 METHOD FOR LIQUID-PHASE SYNTHESIS OF NUCLEIC ACID RNGTT, POLR2H, POLR2E POLB 31/4885ABL1 2954/4885RIN1 2972/4885
US-10730904-B2 Method for liquid-phase synthesis of nucleic acid RNGTT, POLR2H, POLR2E POLB 46/4885ABL1 2128/4885RIN1 1561/4885

“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.