Boric Acid

Boric Acid

SCHEMBL2835168

OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O.OB(O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 1.00
TSHR P16473 1/20 1.00
TDP1 Q9NUW8 1/20 1.00

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
Boric Acid SCHEMBL8594563 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL1483674 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL1227700 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL168347 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL11061786 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL36976 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL562566 1.00
Boric Acid SCHEMBL2793475 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL21951406 1.00 LMNA (1.00) LMNATSHRTDP1
Boric Acid SCHEMBL12054220 1.00

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1737871-B1 METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BORANES SEMEQUIP INC (US) 2012-10-10 EP claimed
US-8084007-B2 Methods of synthesis of isotropically enriched borohydride and methods of synthesis of isotropically enriched boranes SEMEQUIP INC. (US) 2011-12-27 US claimed
US-20100111801-A1 METHODS OF SYNTHESIS OF ISOTROPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTROPICALLY ENRICHED BORANES SEMEQUIP INC. (US) 2010-05-06 US claimed
US-7641879-B2 Methods of synthesis of isotopically enriched borohydride and methods of synthesis of isotopically enriched boranes SEMEQUIP INC. (US) 2010-01-05 US claimed
EP-1737871-A4 METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BORANES SEMEQUIP INC (US) 2009-04-15 EP claimed
EP-1737871-A2 METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BORANES Semequip, Inc. (US) 2007-01-03 EP claimed
WO-2005074531-A2 METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BORANES SEMEQUIP INC. (US) 2005-08-18 WO claimed
US-20050169827-A1 Methods of synthesis of isotopically enriched borohydride and methods of synthesis of isotopically enriched boranes SEMEQUIP INC. 2005-08-04 US claimed
WO-2000055090-A1 METHOD OF SYNTHESIZING ENRICHED DECABORANE FOR USE IN GENERATING BORON NEUTRON CAPTURE THERAPY PHARMACEUTICALS LOCKHEED MARTIN IDAHO TECHNOLOGIES COMPANY (US) 2000-09-21 WO claimed
US-6086837-A Method of synthesizing enriched decaborane for use in generating boron neutron capture therapy pharmaceuticals BECHTEL BWXT IDAHO, LLC (US) 2000-07-11 US claimed
US-4115521-A Process for the synthesis of decaborane(14) UNION CARBIDE CORPORATION (US) 1978-09-19 US claimed
US-4115520-A Process for the synthesis of tetradecahydroundecaborate compounds UNION CARBIDE CORPORATION (US) 1978-09-19 US claimed
CN-111868116-B Ethylene-alpha-olefin-nonconjugated polyene copolymer, process for producing the same, and use thereof 三井化学株式会社 2022-12-09 CN disclosed
EP-1737871-B1 METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTOPICALLY ENRICHED BORANES SEMEQUIP INC (US) 2012-10-10 EP disclosed
CN-101001829-B Method for synthesizing isotopically enriched boron hydride compound and method for synthesizing isotopically enriched borane SEMEQUIP, INC. (US) 2012-02-22 CN disclosed
CN-101001829-B Method for synthesizing isotopically enriched boron hydride compound and method for synthesizing isotopically enriched borane SEMEQUIP, INC. (US) 2012-02-22 CN disclosed
US-4115521-A Process for the synthesis of decaborane(14) UNION CARBIDE CORPORATION (US) 1978-09-19 US disclosed
US-4115521-A Process for the synthesis of decaborane(14) UNION CARBIDE CORPORATION (US) 1978-09-19 US disclosed
US-4115520-A Process for the synthesis of tetradecahydroundecaborate compounds UNION CARBIDE CORPORATION (US) 1978-09-19 US disclosed
US-4115520-A Process for the synthesis of tetradecahydroundecaborate compounds UNION CARBIDE CORPORATION (US) 1978-09-19 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 (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-20100111801-A1 METHODS OF SYNTHESIS OF ISOTROPICALLY ENRICHED BOROHYDRIDE AND METHODS OF SYNTHESIS OF ISOTROPICALLY ENRICHED BORANES SLC5A11, IPO11, HCN4 LMNA 2187/4885TSHR 3213/4885TDP1 3023/4885

“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.