Phosphonic Acid

Phosphonic Acid

SCHEMBL31291502

CSc1ccc(SC)cc1.O=[PH](O)O.O=[PH]([O-])[O-].[Na+].[Na+]

nearest known ligand 0.43

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 Phosphonic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 1/20 0.36
ALDH1A1 P00352 5/20 0.43
PLK1 P53350 1/20 0.42
NOS3 P29474 2/20 0.39
NOS1 P29475 2/20 0.39
FBP1 P09467 1/20 0.38
HAO1 Q9UJM8 1/20 0.38
TSHR P16473 2/20 0.37
MCL1 Q07820 1/20 0.35
KMT2A Q03164 3/20 0.35
MEN1 O00255 2/20 0.35
LMNA P02545 1/20 0.35
NOX1 Q9Y5S8 1/20 0.35
SMN1; SMN2 Q16637 1/20 0.35
MAPT P10636 1/20 0.35
ALOX12 P18054 1/20 0.35
MAPK1 P28482 1/20 0.35
SLC6A4 P31645 1/20 0.34
IDO1 P14902 1/20 0.34

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
Phosphonic Acid SCHEMBL7177636 0.90 ALDH1A1 (0.50) ALDH1A1PLK1NOS3NOS1FBP1
Phosphonic Acid SCHEMBL8588139 0.76 SLC6A4 (0.41) ALDH1A1PLK1MAPTSLC6A4
Phosphonic Acid SCHEMBL9636974 0.74 KMT2A (0.44) ALDH1A1PLK1NOS3NOS1KMT2A
SCHEMBL83839 0.72 ALDH1A1 (0.58) ALDH1A1PLK1NOS3NOS1PTGS2
SCHEMBL31327828 0.70 ALDH1A1 (0.46) ALDH1A1PLK1NOS3NOS1FBP1
Phosphonic Acid SCHEMBL7761460 0.70 AKR1C3 (0.46) MCL1KMT2AMEN1SMN1; SMN2MAPT
Phosphonic Acid SCHEMBL21174010 0.69
SCHEMBL10726762 0.69 ALDH1A1 (0.44) ALDH1A1PLK1NOS3NOS1FBP1
SCHEMBL7758758 0.67 PLK1 (0.57) ALDH1A1PLK1HAO1TSHRKMT2A
SCHEMBL28993337 0.67 TSHR (0.50) ALDH1A1TSHRPTGS2KMT2AMEN1

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 1 patent. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119212712-A Proliferation or differentiation inducer for chondrocytes 国立大学法人东北大学 2024-12-27 CN disclosed