Benzylphosphonic Acid

Benzylphosphonic Acid

SCHEMBL1880404

O=P([O-])(O)Cc1ccccc1.[Na+]

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Benzylphosphonic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FDPS known ✓ P14324 1/20 0.45
HPGD P15428 1/20 0.54
TSHR P16473 2/20 0.47
CES2 O00748 1/20 0.44
CES1 P23141 1/20 0.44
LAP3 P28838 3/20 0.44
ANPEP P15144 3/20 0.44
HDAC3 O15379 1/20 0.44
HDAC4 P56524 1/20 0.44
HDAC1 Q13547 1/20 0.44
HDAC7 Q8WUI4 1/20 0.44
HDAC2 Q92769 1/20 0.44
HDAC10 Q969S8 1/20 0.44
HDAC11 Q96DB2 1/20 0.44
HDAC8 Q9BY41 1/20 0.44
HDAC6 Q9UBN7 1/20 0.44
HDAC9 Q9UKV0 1/20 0.44
HDAC5 Q9UQL6 1/20 0.44
ACP3 P15309 1/20 0.42
CFTR P13569 1/20 0.41

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
Benzylphosphonic Acid SCHEMBL914506 0.81 HPGD (0.52) HPGDTSHRFDPSCES2CES1
Benzylphosphonic Acid SCHEMBL7644922 0.79 CETP (0.44) HPGD
Tetrabuthylammonium SCHEMBL7643383 0.79 CETP (0.48)
SCHEMBL497159 0.78 HPGD (0.60) HPGDTSHRFDPSLAP3ANPEP
Benzylphosphonic Acid SCHEMBL44318 0.78 HPGD (0.60) HPGDTSHRLAP3ANPEPACP3
SCHEMBL9179278 0.77 KMT2A (0.47) HPGDHDAC3HDAC4HDAC1HDAC2
SCHEMBL17004009 0.76 HPGD (0.58) HPGDTSHRFDPSLAP3ANPEP
SCHEMBL8371905 0.76 TSHR (0.57) HPGDTSHRFDPSLAP3ANPEP
Benzylphosphonic Acid SCHEMBL915222 0.76 HPGD (0.58) HPGDTSHRLAP3ANPEPACP3
Benzylphosphonic Acid SCHEMBL9182475 0.76 HPGD (0.52) HPGDTSHRFDPSCES2CES1

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-8815834-B2 Use of dendrimers to stimulate cell growth CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2014-08-26 US disclosed
US-20110106053-A1 TREATMENT APPARATUS Elanco New Zealand (NZ) 2011-05-05 US disclosed
US-20090142316-A1 Use of Dendrimers to Stimulate Cell Growth CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2009-06-04 US disclosed
WO-2009022922-A1 TREATMENT APPARATUS BOMAC RESEARCH LIMITED (NZ) 2009-02-19 WO disclosed
US-3984501-A PROSTAGLANDIN INHIBITORS NELSON RESEARCH & DEVELOPMENT COMPANY (US) 1976-10-05 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-20090142316-A1 Use of Dendrimers to Stimulate Cell Growth HDGF, CD40LG, PPIP5K2 FDPS 785/4885HPGD 1364/4885TSHR 383/4885

“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.