Phosphoric Acid

Phosphoric Acid

SCHEMBL216583

Nc1ncnc2c1ncn2[C@]1(P(=O)(O)O)O[C@H](CO)[C@@H](O)[C@H]1O.O=P(O)(O)O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

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 20)

geneUniProtsupporting neighboursconfidence
DPP4 known ✓ P27487 1/20 0.48
ADRB2 known ✓ P07550 1/20 0.45
KCNH2 known ✓ Q12809 1/20 0.45
ADORA1 P30542 3/20 0.50
ADORA3 P0DMS8 4/20 0.48
ADORA2A P29274 3/20 0.48
PI4KA P42356 2/20 0.48
PI4K2B Q8TCG2 2/20 0.48
PI4K2A Q9BTU6 2/20 0.48
PI4KB Q9UBF8 2/20 0.48
SLC28A1 O00337 2/20 0.48
SMN1; SMN2 Q16637 2/20 0.48
MEN1 O00255 1/20 0.48
MAP3K7 O43318 1/20 0.48
SLC28A2 O43868 1/20 0.48
GAPDH P04406 1/20 0.48
MAPK1 P28482 1/20 0.48
ADORA2B P29275 1/20 0.48
STAT6 P42226 1/20 0.48
KMT2A Q03164 1/20 0.48

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
SCHEMBL199259 0.99 ADORA1 (0.51) ADORA1ADORA3ADORA2API4KAPI4K2B
Pyrophosphoric Acid SCHEMBL668584 0.94 ADORA1 (0.52) ADORA1ADORA3ADORA2API4KAPI4K2B
SCHEMBL15665475 0.88 ADORA1 (0.52) ADORA1ADORA3ADORA2API4KAPI4K2B
SCHEMBL8572697 0.87 ADORA1 (0.38) ADORA1ADORA3ADORA2API4KAPI4K2B
SCHEMBL214972 0.87 P2RY1 (0.59) ADORA1SMN1; SMN2DNPH1PRKAB2TRPM2
SCHEMBL27971039 0.86 FDPS (0.42) ADORA1ADORA3ADORA2API4KAPI4K2B
SCHEMBL13738525 0.86 ADORA1 (0.38) ADORA1ADORA3ADORA2API4KAPI4K2B
Phosphoric Acid SCHEMBL23802568 0.85 ADORA1 (0.50) ADORA1ADORA3ADORA2API4KAPI4K2B
Phosphoric Acid SCHEMBL15201527 0.85 PI4KA (0.51) ADORA1ADORA3ADORA2API4KAPI4K2B
SCHEMBL668586 0.83 P2RX1 (0.59) ADORA1SMN1; SMN2DNPH1PRKAB2TRPM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118109378-A Coli engineering bacterium for high-yield L-methionine and method for producing L-methionine by full fermentation method thereof 浙江工业大学 2024-05-31 CN disclosed
CN-114846143-A Expression of nitrogenase polypeptides in plant cells 联邦科学技术研究组织 2022-08-02 CN disclosed
CN-114144527-A Expression of nitrogenase polypeptides in plant cells 联邦科学技术研究组织 2022-03-04 CN disclosed
US-8088897-B2 Detecting the activity of and screening acceptor substrates, inhibitors, or activators of enzymes catalyzing group transfer reactions to facilitate the development of more selective and therapeutic drugs BellBrook Labs, Inc. (US) 2012-01-03 US disclosed
US-7847066-B2 High throughput screening; immunoassays; immunogens; antibodies producing uridine diphosphate with higher affinity to carbohydrates BELLBROOK LABS, LLC (US) 2010-12-07 US disclosed
EP-2222708-A1 ASSAY METHOD FOR GROUP TRANSFER REACTIONS Bellbrook Labs, Llc (US) 2010-09-01 EP disclosed
US-20090186358-A1 Pathway Analysis of Cell Culture Phenotypes and Uses Thereof WYETH (US) 2009-07-23 US disclosed
WO-2009078876-A1 ASSAY METHOD FOR GROUP TRANSFER REACTIONS BELLBROOK LABS, LLC (US) 2009-06-25 WO disclosed
US-20080255341-A2 ASSAY METHOD FOR GROUP TRANSFER REACTIONS LOWERY ROBERT 2008-10-16 US disclosed
US-20080233592-A1 Assay Method for Group Transfer Reactions BELLBROOK LABS, LLC 2008-09-25 US disclosed
US-20080188439-A1 Directed metabolism of compounds by glucuronidation and sulfonation donors to decrease toxicity SALHANICK STEVEN D 2008-08-07 US disclosed
US-20080132684-A1 Assay Method for Group Transfer Reactions LOWERY ROBERT 2008-06-05 US disclosed
US-7378505-B2 Assay method for group transfer reactions BELLBROOK LABS LLC (US) 2008-05-27 US disclosed
US-7355010-B2 Assay method for group transfer reactions BELLBROOK LABS, LLC (US) 2008-04-08 US disclosed
EP-1869083-A1 ASSAY METHOD FOR GROUP TRANSFER REACTIONS BellBrook Labs, LLC (US) 2007-12-26 EP disclosed
WO-2006127008-A1 ASSAY METHOD FOR GROUP TRANSFER REACTIONS BELLBROOK LABS, LLC (US) 2006-11-30 WO disclosed
US-20060172335-A1 Assay method for group transfer reactions NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2006-08-03 US disclosed
US-20050239142-A1 Assay method for group transfer reactions NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2005-10-27 US disclosed