SCHEMBL1582963

SCHEMBL1582963

CCCCCC(OC(c1ccccc1)(c1ccc(OC)cc1)c1ccc(OC)cc1)[C@H]1O[C@@H](n2cnc3c(N)ncnc32)[C@H](OC)[C@@H]1OP(OCCC#N)N(C(C)C)C(C)C

nearest known ligand 0.34

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
TRDMT1 O14717 1/20 0.34
NNMT P40261 2/20 0.34
ADORA1 P30542 2/20 0.34
EHMT1 Q9H9B1 1/20 0.34
CARM1 Q86X55 2/20 0.33
AHCY P23526 1/20 0.33
TYMP P19971 1/20 0.33
DOT1L Q8TEK3 1/20 0.32
ADORA3 P0DMS8 1/20 0.31

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
SCHEMBL1583282 0.93 NNMT (0.33) TRDMT1NNMTADORA1EHMT1CARM1
SCHEMBL6443389 0.89 HPGD (0.37) TYMP
SCHEMBL6895651 0.86 AHCY (0.35) TRDMT1NNMTCARM1AHCYDOT1L
SCHEMBL6898692 0.86 AHCY (0.35) TRDMT1NNMTCARM1AHCYDOT1L
SCHEMBL8583121 0.83 P2RX3 (0.39) TRDMT1NNMTADORA1CARM1DOT1L
SCHEMBL2109084 0.83 TRDMT1 (0.36) TRDMT1NNMTADORA1CARM1AHCY
SCHEMBL15879332 0.82 TRDMT1 (0.36) TRDMT1NNMTADORA1CARM1AHCY
SCHEMBL1582886 0.82 EHMT1 (0.47) TRDMT1NNMTADORA1EHMT1CARM1
SCHEMBL7914645 0.81 TRDMT1 (0.37) TRDMT1NNMTADORA1CARM1AHCY
SCHEMBL4557136 0.80 NNMT (0.34) TRDMT1NNMTADORA1CARM1TYMP

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
EP-1313752-B1 METHODS FOR SYNTHESIZING NUCLEOSIDE DERIVATIVES RIBOZYME PHARM INC (US) 2011-04-20 EP disclosed
US-20050059817-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives SIRNA THERAPEUTICS, INC. (US) 2005-03-17 US disclosed
US-6686463-B2 FEWER SYNTHETIC STEPS; INVOLVES FORMATION OF A 5',4'-BRIDGING SILYL PROTECTING GROUP TO FORM A FUSED SILOXANE ON THE FURAN RING SIRNA THERAPEUTICS, INC. 2004-02-03 US disclosed
US-20020150936-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives RIBOZYME PHARMACEUTICALS, INC. 2002-10-17 US disclosed
US-20020120129-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives RIBOZYME PHARMACEUTICALS, INC. 2002-08-29 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 (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-20050059817-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B TRDMT1 68/4885NNMT 22/4885ADORA1 652/4885
US-20020120129-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B TRDMT1 96/4885NNMT 22/4885ADORA1 826/4885
US-20020150936-A1 Methods for synthesizing nucleosides, nucleoside derivatives and non-nucleoside derivatives PNP, NSUN2, NT5C3B TRDMT1 69/4885NNMT 19/4885ADORA1 887/4885

“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.