SCHEMBL3918261

SCHEMBL3918261

O=C(NO)c1c(O)cccc1O

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 2/20 0.58
MPO P05164 1/20 0.58
GAA P10253 1/20 0.58
SMN1; SMN2 Q16637 1/20 0.58
HIF1A Q16665 1/20 0.58
CA12 O43570 5/20 0.54
CA1 P00915 5/20 0.54
CA9 Q16790 5/20 0.54
CA2 P00918 4/20 0.54
CA7 P43166 4/20 0.54
CA14 Q9ULX7 4/20 0.54
TAS1R3 Q7RTX0 1/20 0.53
TAS1R1 Q7RTX1 1/20 0.53
TAS1R2 Q8TE23 1/20 0.53
THRB P10828 1/20 0.52
EGLN2 Q96KS0 1/20 0.48
HDAC6 Q9UBN7 5/20 0.46
HDAC8 Q9BY41 4/20 0.46
HDAC1 Q13547 3/20 0.46
HDAC3 O15379 1/20 0.46

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
SCHEMBL619724 0.85 CES2 (0.50) KDM4EMPOGAASMN1; SMN2HIF1A
SCHEMBL14880049 0.80 CA1 (0.55) KDM4ECA12CA1CA9CA2
SCHEMBL6501339 0.78 CA12 (0.58) KDM4EGAACA12CA1CA9
SCHEMBL8424844 0.78 CA1 (0.52) KDM4EMPOGAAHIF1ACA12
SCHEMBL9314455 0.78 HDAC6 (0.48) KDM4EMPOGAASMN1; SMN2HIF1A
SCHEMBL29638147 0.78 HDAC1 (0.45) KDM4EMPOGAASMN1; SMN2HIF1A
SCHEMBL9313956 0.75 CYP3A4 (0.52) KDM4EMPOGAASMN1; SMN2HIF1A
SCHEMBL1436240 0.75 GAA (0.69) KDM4EMPOGAASMN1; SMN2HIF1A
SCHEMBL6992219 0.73 CES2 (0.58) KDM4EGAATHRBHDAC6HDAC1
Salicylhydroxamic Acid SCHEMBL21530845 0.73 KDM4E (1.00) KDM4EMPOGAASMN1; SMN2HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7524941-B2 Methods for the preparation of chemically misaminoacylated tRNA via protective groups AMBERGEN, INC. (US) 2009-04-28 US disclosed
US-20080287710-A1 Methods for the preparation of chemically misaminoacylated tRNA via protective groups AMBERGEN, INC. 2008-11-20 US disclosed
EP-1472372-A4 METHODS FOR THE PREPARATION OF CHEMICALLY MISAMINOACYLATED tRNA VIA PROTECTIVE GROUPS AMBERGEN INC (US) 2008-08-13 EP disclosed
US-7288372-B2 Methods for the preparation of chemically misaminoacylated tRNA via protective groups AMBERGEN, INC. (US) 2007-10-30 US disclosed
EP-1165569-B1 BORONIC ACID CONTAINING REAGENTS AND OLIGONUCLEOTIDES AGILENT TECHNOLOGIES INC (US) 2005-08-10 EP disclosed
US-6870065-B2 Bifunctional boronic compound complexing reagents and complexes CAMBREX BIO SCIENCE ROCKLAND, INC. (US) 2005-03-22 US disclosed
EP-1472372-A1 METHODS FOR THE PREPARATION OF CHEMICALLY MISAMINOACYLATED tRNA VIA PROTECTIVE GROUPS Ambergen, Inc. (US) 2004-11-03 EP disclosed
US-20040072203-A1 Purification of primer extension products PROLINX, INC. 2004-04-15 US disclosed
US-20030219780-A1 Methods for the preparation of chemically misaminoacylated tRNA via protective groups AMBERGEN, INC. 2003-11-27 US disclosed
US-6630577-B2 Useful for producing bioconjugates PROLINX, INC. 2003-10-07 US disclosed
EP-0915832-A1 BORONIC COMPOUND COMPLEXING REAGENTS AND HIGHLY STABLE COMPLEXES PROLINX, INC. (US) 1999-05-19 EP disclosed
US-5877297-A Boronic compound complexing reagents and highly stable complexes PROLINX, INC. (US) 1999-03-02 US disclosed
US-5876938-A Use of boron-containing polynucleotides as diagnostic agents PROLINX, INCORPORATED (US) 1999-03-02 US disclosed
US-5872224-A Boronic compound complexing reagents and highly stable complexes PROLINX, INC. (US) 1999-02-16 US disclosed
US-5837878-A Boronic compound complexing reagents and highly stable complexes PROLINX, INC. (US) 1998-11-17 US disclosed
US-5831045-A Boronic acid-containing polynucleotides PORLINX, INCORPORATED (US) 1998-11-03 US disclosed
US-5831046-A Boronic acid-contaning nucleic acid monomers PROLINX, INCORPORATED (US) 1998-11-03 US disclosed
US-5777148-A Boronic compound complexing reagents and highly stable complexes PROLINX, INC. (US) 1998-07-07 US disclosed
WO-1998005672-A1 NOVEL BORONIC ACID-CONTAINING NUCLEIC ACIDS AND THEIR USE AS DIAGNOSTIC AGENTS PROLINX INCORPORATED (US) 1998-02-12 WO disclosed
WO-1998005627-A1 BORONIC COMPOUND COMPLEXING REAGENTS AND HIGHLY STABLE COMPLEXES PROLINX, INC. (US) 1998-02-12 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 (2 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-20080287710-A1 Methods for the preparation of chemically misaminoacylated tRNA via protective groups NSUN3, TRMT1, TARBP1 KDM4E 2377/4885MPO 2921/4885GAA 1537/4885
US-20030219780-A1 Methods for the preparation of chemically misaminoacylated tRNA via protective groups NSUN3, TRMT1, TARBP1 KDM4E 2377/4885MPO 2921/4885GAA 1537/4885

“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.