Phenylboronic Acid

Phenylboronic Acid

SCHEMBL988758

OB(O)c1ccccc1.c1ccc(C(c2ccccc2)(c2ccccc2)n2cnnn2)cc1

nearest known ligand 0.44

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA4 P22748 1/20 0.44
CA6 P23280 1/20 0.44
CA5A P35218 1/20 0.44
CA7 P43166 1/20 0.44
ENPP2 Q13822 1/20 0.44
CA14 Q9ULX7 1/20 0.44
CA5B Q9Y2D0 1/20 0.44
NOTUM Q6P988 2/20 0.36
MGLL Q99685 4/20 0.35
CA1 P00915 2/20 0.35
CA2 P00918 2/20 0.35
CYP11B1 P15538 1/20 0.33
CYP11B2 P19099 1/20 0.33
TRPV6 Q9H1D0 2/20 0.31
PCSK9 Q8NBP7 1/20 0.31
ORAI1 Q96D31 1/20 0.31
ORAI2 Q96SN7 1/20 0.31
ORAI3 Q9BRQ5 1/20 0.31
ALDH1A1 P00352 1/20 0.31
NPSR1 Q6W5P4 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
SCHEMBL198143 0.87 NOTUM (0.45) NOTUMCA2CYP11B1CYP11B2ALDH1A1
SCHEMBL4876723 0.75 NOTUM (0.38) NOTUMCYP11B1CYP11B2ALDH1A1NPSR1
SCHEMBL16975525 0.74 KIF11 (0.37) NOTUMCYP11B1CYP11B2ALDH1A1NPSR1
SCHEMBL2360873 0.72 KCNN4 (0.57) NOTUMCA2CYP11B1CYP11B2ALDH1A1
Phenylboronic Acid SCHEMBL9403416 0.72 CA4 (0.44) CA4CA6CA5ACA7ENPP2
SCHEMBL8987731 0.69 NOTUM (0.42) NOTUMCYP11B1CYP11B2ALDH1A1NPSR1
SCHEMBL369213 0.69 CA4 (0.39) CA4CA6CA5ACA7ENPP2
Phenylboronic Acid SCHEMBL8628436 0.66 ENPP2 (1.00) CA4CA6CA5ACA7ENPP2
Phenylboronic Acid SCHEMBL4453 0.66
SCHEMBL3256000 0.66 CA1 (0.43) CA4CA6CA5ACA7ENPP2

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-7868180-B2 Process for the preparation of sartan derivatives and intermediates useful in such process KRKA, D.D. NOVO MESTO (SI) 2011-01-11 US disclosed
US-20080312451-A1 Process For the Preparation of Sartan Derivatives and Intermediates Useful in Such Process KRKA, D.D. NOVO MESTO (SK) 2008-12-18 US disclosed
EP-1931655-A2 A PROCESS FOR THE PREPARATION OF SARTAN DERIVATIVES AND INTERMEDIATES USEFUL IN SUCH PROCESS KRKA, D.D., Novo Mesto (SI) 2008-06-18 EP disclosed
WO-2007039117-A2 A PROCESS FOR THE PREPARATION OF SARTAN DERIVATIVES AND INTERMEDIATES USEFUL IN SUCH PROCESS KRKA, D.D., NOVO, MESTO (SI) 2007-04-12 WO disclosed
EP-1764365-A1 A process for the preparation of sartan derivates and intermediates useful in such process KRKA, D.D., Novo Mesto (SI) 2007-03-21 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 (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-20080312451-A1 Process For the Preparation of Sartan Derivatives and Intermediates Useful in Such Process MC5R, NPY5R, ADRA1D CA4 997/4885CA6 474/4885CA5A 409/4885

“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.