Phosphoric Acid — predicted protein targets

Known targets — ChEMBL curated mechanism

ADRA1A ADRA1B ADRA1D ADRB1 ADRB2 ADRB3 CYP11B1 DPP4 FGFR1 FGFR2 FGFR3 FGFR4 HRH1 JAK1 JAK2 JAK3 KCNA1 KCNA10 KCNA2 KCNA3 KCNA4 KCNA5 KCNA6 KCNA7 KCNB1 KCNB2 KCNC1 KCNC2 KCNC3 KCNC4 KCND1 KCND2 KCND3 KCNF1 KCNG1 KCNG2 KCNG3 KCNG4 KCNH1 KCNH2 KCNH3 KCNH4 KCNH5 KCNH6 KCNH7 KCNH8 KCNQ1 KCNQ2 KCNQ3 KCNQ4 KCNQ5 KCNS1 KCNS2 KCNS3 KCNV1 KCNV2 KDR KIT NA OPRD1 OPRK1 OPRM1 P PDGFRB PIK3CD SCN10A SCN11A SCN1A SCN2A SCN3A SCN4A SCN5A SCN7A SCN8A SCN9A SMO TYK2 pol rplA rplB rplC rplD rplE rplF rplJ rplK rplL rplM rplN rplO rplP rplQ rplR rplS rplT rplU rplV rplW rplX rplY rpmA rpmB rpmC rpmD rpmE rpmF rpmG rpmH rpmI rpmJ rpsA rpsB rpsC rpsD rpsE rpsF rpsG rpsH rpsI rpsJ rpsK rpsL rpsM rpsN rpsO rpsP rpsQ rpsR rpsS rpsT rpsU ykgM ykgO

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

Predicted protein targets (top 14)

	gene	UniProt	supporting neighbours	confidence
▸	FDPS	P14324	3/20	0.42

▸	MEN1	O00255	1/20	0.37

▸	APAF1	O14727	1/20	0.37

▸	NPC1	O15118	1/20	0.37

▸	PLA2G1B	P04054	1/20	0.37

▸	HSP90AA1	P07900	1/20	0.37

▸	MAPT	P10636	1/20	0.37

▸	MAPK1	P28482	1/20	0.37

▸	HTT	P42858	1/20	0.37

▸	RAB9A	P51151	1/20	0.37

▸	KMT2A	Q03164	1/20	0.37

▸	SMN1; SMN2	Q16637	1/20	0.37

▸	NPSR1	Q6W5P4	1/20	0.37

▸	ATG4B	Q9Y4P1	1/20	0.37

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.

Compound	similarity	top predicted	shared targets
Methyl Phosphonate SCHEMBL15388239	0.93	FDPS (0.41)	FDPSMEN1APAF1NPC1PLA2G1B
SCHEMBL19281745	0.91	FDPS (0.40)	FDPSMEN1APAF1NPC1PLA2G1B
SCHEMBL15348132	0.91	FDPS (0.40)	FDPSMEN1APAF1NPC1PLA2G1B
Pyrophosphoric Acid SCHEMBL20490686	0.88	FDPS (0.38)	FDPSMEN1APAF1NPC1PLA2G1B
Phosphoric Acid Monomethyl Ester SCHEMBL4790556	0.88	FDPS (0.38)	FDPSMEN1APAF1NPC1PLA2G1B
Phosphoric Acid SCHEMBL28525368	0.86	FDPS (0.42)	FDPSMEN1APAF1NPC1PLA2G1B
Phosphoric Acid SCHEMBL20490689	0.86	FDPS (0.42)	FDPSMEN1APAF1NPC1PLA2G1B
SCHEMBL412652	0.86	FDPS (0.37)	FDPS
Fluoride SCHEMBL28440237	0.85	—	—
SCHEMBL35176	0.85	—	—

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

Patent	Title	Assignee	Published	Priority	Filing	Country	Status
CN-111117594-B	Electrochromic material and electrochromic device based on dynamic metal-ligand complexation	吉林大学	2024-03-26	—	—	CN	claimed
CN-111051469-B	Acid stabilization of quantum dot-resin concentrates and premixes	昭荣化学工业株式会社	2024-06-04	—	—	CN	disclosed
CN-112430855-B	Preparation method of homogeneous spinning solution	郑州中远氨纶工程技术有限公司	2022-03-08	—	—	CN	disclosed
CN-112430855-A	Preparation method of homogeneous spinning solution	郑州中远氨纶工程技术有限公司	2021-03-02	—	—	CN	disclosed
WO-2008098032-A2	USE OF LIGNOCELLULOSICS SOLVATED IN IONIC LIQUIDS FOR PRODUCTION OF BIOFUELS	NORTH CAROLINA STATE UNIVERSITY (US)	2008-08-14	—	—	WO	disclosed
WO-2008098036-A1	PRODUCT PREPARATION AND RECOVERY FROM THERMOLYSIS OF LIGNOCELLULOSICS IN IONIC LIQUIDS	NORTH CAROLINA STATE UNIVERSITY (US)	2008-08-14	—	—	WO	disclosed
WO-2008098037-A2	POLYMER DERIVATIVES AND COMPOSITES FROM THE DISSOLUTION OF LIGNOCELLULOSICS IN IONIC LIQUIDS	NORTH CAROLINA STATE UNIVERSITY (US)	2008-08-14	—	—	WO	disclosed