SCHEMBL3485699

SCHEMBL3485699

CC(C)C(=O)OC[C@H]1O[C@@H](n2cnc3c(=O)[nH]c(N)nc32)C[C@@H]1NC(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HINT1 P49773 6/20 0.49
POLB P06746 1/20 0.48
TAAR1 Q96RJ0 2/20 0.46
TAS1R3 Q7RTX0 1/20 0.46
TAS1R1 Q7RTX1 1/20 0.46
TYMP P19971 1/20 0.45
GSK3A P49840 2/20 0.45
RPS6KA3 P51812 2/20 0.45
MAPK14 Q16539 2/20 0.45
P2RY2 P41231 1/20 0.43
P2RY4 P51582 1/20 0.43
P2RY6 Q15077 1/20 0.43
KDM4E B2RXH2 1/20 0.42
PNP P00491 1/20 0.42
NT5E P21589 1/20 0.40
KRAS P01116 1/20 0.40

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
SCHEMBL367384 0.82 POLB (0.65) HINT1POLBTAAR1TYMPGSK3A
SCHEMBL16609224 0.82 KDM4E (0.56) HINT1POLBTAAR1TAS1R3TAS1R1
SCHEMBL24852831 0.81 POLB (0.53) HINT1POLBTAAR1TAS1R3TAS1R1
SCHEMBL17279179 0.80 KDM4E (0.54) HINT1POLBTAAR1TAS1R3TAS1R1
SCHEMBL7517850 0.80 KDM4E (0.54) HINT1POLBTAAR1TAS1R3TAS1R1
SCHEMBL8665070 0.80 KDM4E (0.62) POLBTAAR1TAS1R3TAS1R1TYMP
SCHEMBL17279165 0.80 KDM4E (0.62) POLBTAAR1TAS1R3TAS1R1TYMP
SCHEMBL6470562 0.80 KDM4E (0.62) POLBTAAR1TAS1R3TAS1R1TYMP
SCHEMBL7562193 0.80 POLB (0.51) HINT1POLBTAS1R3TAS1R1GSK3A
SCHEMBL16609168 0.79 KDM4E (0.52) POLBTAS1R3TAS1R1TYMPP2RY2

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 21 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9572891-B2 Oligonucleotide conjugates GERON CORPORATION (US) 2017-02-21 US disclosed
US-20150374841-A1 Oligonucleotide Conjugates GERON CORPORATION 2015-12-31 US disclosed
US-9072790-B2 Oligonucleotide conjugates GERON CORPORATION (US) 2015-07-07 US disclosed
US-20140349292-A1 OLIGONUCLEOTIDE N3'-->P5' THIOPHOSPHORAMIDATES: THEIR SYNTHESIS AND USE GERON CORPORATION 2014-11-27 US disclosed
EP-1543021-B1 OLIGONUCLEOTIDE CONJUGATES GERON CORP (US) 2014-07-30 EP disclosed
US-20130253042-A1 Oligonucleotide Conjugates GERON CORPORATION (US) 2013-09-26 US disclosed
EP-1379689-B1 OLIGONUCLEOTIDE CONJUGATES GERON CORP (US) 2012-09-26 EP disclosed
US-20100016416-A1 Oligonucleotide Conjugates GERON CORPORATION (US) 2010-01-21 US disclosed
US-7563618-B2 Oligonucleotide conjugates GERON CORPORATION (US) 2009-07-21 US disclosed
EP-1992634-A1 Oligonucleotide n3'- p5' thiophosphoramidates: their synthesis and use Geron Corporation (US) 2008-11-19 EP disclosed
US-20070037770-A1 That retains the high RNA binding affinity of the parent oligonucleotide N3' --> P5' phosphoramidates and exhibits a much higher acid stability; inhibiting human telomerase enzyme activity; solid phase synthesis; kits GERON CORPORATION 2007-02-15 US disclosed
US-7138383-B2 That retains the high RNA binding affinity of the parent oligonucleotide N3' --> P5' phosphoramidates and exhibits a much higher acid stability; inhibiting human telomerase enzyme activity GERON CORPORATION (US) 2006-11-21 US disclosed
US-20050049408-A1 That retains the high RNA binding affinity of the parent oligonucleotide N3' --> P5' phosphoramidates and exhibits a much higher acid stability; inhibiting human telomerase enzyme activity; solid phase synthesis; kits GERON CORPORATION 2005-03-03 US disclosed
US-6835826-B2 Acid resistance, stability; telomerase inhibitor GERON CORPORATION 2004-12-28 US disclosed
US-20030212032-A1 Acid resistance, stability; telomerase inhibitor GERON CORPORATION 2003-11-13 US disclosed
US-6608036-B1 Inhibit telomerase enzyme activity; inhibit proliferation of cell that expresses telomerase GERON CORPORATION 2003-08-19 US disclosed
US-20030138814-A1 Comprises RNA and nucleobase/fluorophore for inhibition of human telomerase activity (inhibits growth of cancerous cells) GERON CORPORATION 2003-07-24 US disclosed
EP-0882059-B1 SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDE N3-'P5'- PHOSPHORAMIDATES LYNX THERAPEUTICS INC (US) 2002-02-06 EP disclosed
EP-0882059-A1 SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDE N3-'P5'- PHOSPHORAMIDATES LYNX THERAPEUTICS, INC. (US) 1998-12-09 EP disclosed
WO-1997031009-A1 SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDE N3'→P5' PHOSPHORAMIDATES LYNX THERAPEUTICS, INC. (US) 1997-08-28 WO 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 (8 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-20150374841-A1 Oligonucleotide Conjugates TERT, RNGTT, TRDMT1 HINT1 1632/4885POLB 79/4885TAAR1 2259/4885
US-20130253042-A1 Oligonucleotide Conjugates TERT, RNGTT, TRDMT1 HINT1 1632/4885POLB 79/4885TAAR1 2259/4885
US-20050049408-A1 That retains the high RNA binding affinity of the parent oligonucleotide N3' --> P5' phosphoramidates and exhibits a much higher acid stability; inhibiting human telomerase enzyme activity; solid phase synthesis; kits RNGTT, MTAP, TYMP HINT1 186/4885POLB 202/4885TAAR1 4331/4885
US-20030138814-A1 Comprises RNA and nucleobase/fluorophore for inhibition of human telomerase activity (inhibits growth of cancerous cells) TERT, RNGTT, DUT HINT1 1254/4885POLB 151/4885TAAR1 1976/4885
US-20030212032-A1 Acid resistance, stability; telomerase inhibitor NT5C3B, MTAP, TERT HINT1 167/4885POLB 304/4885TAAR1 3950/4885
US-20070037770-A1 That retains the high RNA binding affinity of the parent oligonucleotide N3' --> P5' phosphoramidates and exhibits a much higher acid stability; inhibiting human telomerase enzyme activity; solid phase synthesis; kits RNGTT, MTAP, TYMP HINT1 186/4885POLB 202/4885TAAR1 4331/4885
US-20140349292-A1 OLIGONUCLEOTIDE N3'-->P5' THIOPHOSPHORAMIDATES: THEIR SYNTHESIS AND USE MTAP, NT5C3B, RNGTT HINT1 99/4885POLB 398/4885TAAR1 4439/4885
US-20100016416-A1 Oligonucleotide Conjugates TERT, RNGTT, TRDMT1 HINT1 1632/4885POLB 79/4885TAAR1 2259/4885

“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.