Phosphonic Acid

Phosphonic Acid

SCHEMBL5159602

CCC(CC)(OC)c1cc(OC)cc([N+](=O)[O-])c1.O=[PH](O)O

nearest known ligand 0.38

Full drug profile on Sugi Atlas →

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 8/20 0.38
KMT2A Q03164 8/20 0.38
MAPT P10636 4/20 0.38
LMNA P02545 2/20 0.38
MAPK1 P28482 2/20 0.38
HTT P42858 2/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
ALDH1A1 P00352 1/20 0.37
POLB P06746 1/20 0.37
PTGS1 P23219 1/20 0.36
PTGS2 P35354 1/20 0.36
ALOX5 P09917 1/20 0.35
NPSR1 Q6W5P4 1/20 0.34
NPC1 O15118 1/20 0.33
L3MBTL1 Q9Y468 2/20 0.33
ERN1 O75460 1/20 0.33

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 SCHEMBL7599302 0.78 ALDH1A1 (0.32) KMT2AALDH1A1POLB
Phosphonic Acid SCHEMBL5162936 0.78 MARS1 (0.32) MEN1KMT2APOLB
Phosphonic Acid SCHEMBL5164460 0.74 ELANE (0.37) KMT2ASMN1; SMN2POLB
SCHEMBL1975027 0.74 ALDH1A1 (0.39) KMT2AMAPK1HTTSMN1; SMN2ALDH1A1
Phosphonic Acid SCHEMBL8583461 0.73 CES2 (0.40) MEN1KMT2AMAPTLMNAMAPK1
SCHEMBL444951 0.72 LMNA (0.45) MEN1KMT2AMAPTLMNAMAPK1
SCHEMBL309863 0.71 LMNA (0.61) MEN1KMT2AMAPTLMNAMAPK1
SCHEMBL8008016 0.71 PTGS1 (0.59) MEN1KMT2AMAPTLMNAMAPK1
SCHEMBL4974489 0.69 MEN1 (0.40) MEN1KMT2AMAPTLMNAMAPK1
Phosphonic Acid SCHEMBL8581175 0.68 CYP1A2 (0.41) MAPTLMNASMN1; SMN2ALDH1A1PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1120423-B1 Improved chemiluminescent 1,2-dioxetanes APPLERA CORP (US) 2007-03-14 EP disclosed
US-6346615-B1 SPIROADAMANTYL DIOXETANES BEARING AN ALKOXY SUBSTITUENT, AND AN AROMATIC SUBSTITUENT ON THE DIOXETANE RING CAN BE ACTIVATED TO CHEMILUMINESCE IF THE AROMATIC SUBSTITUENT BEARS A MOIETY THAT IS CLEAVED BY AN ENZYME TROPIX, INC. 2002-02-12 US disclosed
US-6140495-A SPIROADAMANTYL DIOXETANES BEARING AN ALKOXY SUBSTITUENT AND AN AROMATIC SUBSTITUENT OF PHENYL OR NAPHTHYL ON THE DIOXETANE RING; REPORTER MOLECULES FOR MEASUREMENT OF ENZYMATIC ACTIVITY TROPIX, INC. (US) 2000-10-31 US disclosed
US-6022964-A SPIROADAMANTYL DIOXETANES WITH AN ALKOXY SUBSTITUENT AND A NAPHTHYL SUBSTITUENT ON THE DIOXETANE RING WHICH CAN BE ACTIVATED BY ENZYMATIC CLEAVAGE OF LABILE GROUP; KINETICS AND SIGNAL INTENSITY DEPENDS ON ELECTRON-ACTIVATING GROUP TROPIX, INC. (US) 2000-02-08 US disclosed
US-5851771-A Chemiluminescent 1,2-dioxetanes TROPIX, INC. (US) 1998-12-22 US disclosed
US-5840919-A SPIROADAMANTYL 1,2-DIOXETANES CHARACTERIZED BY SUBSTITUENT ON AROMATIC RING IN ADDITION TO META-SUBSTITUTED ENZYME-LABILE GROUP TROPIX, INC. (US) 1998-11-24 US disclosed
US-5538847-A Chemiluminescent 1,2-dioxetanes TROPIX, INC. (US) 1996-07-23 US disclosed
EP-0649417-A1 IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES TROPIX, INC. (US) 1995-04-26 EP disclosed
EP-0649417-A4 IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES. TROPIX INC (US) 1995-02-27 EP disclosed
WO-1994026726-A1 IMPROVED CHEMILUMINESCENT 1,2-DIOXETANES TROPIX, INC. (US) 1994-11-24 WO disclosed