Phosphoric Acid

Phosphoric Acid

SCHEMBL6689741

CC(C)(C[Sn](CC(C)(C)c1ccccc1)(CC(C)(C)c1ccccc1)O[Sn](CC(C)(C)c1ccccc1)(CC(C)(C)c1ccccc1)CC(C)(C)c1ccccc1)c1ccccc1.O=P(O)(O)O

nearest known ligand 0.41

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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
TAAR1 Q96RJ0 1/20 0.41
PTPN1 P18031 1/20 0.40
POLB P06746 2/20 0.38
CYP2C19 P33261 2/20 0.38
HIF1A Q16665 1/20 0.38
ALDH1A1 P00352 2/20 0.37
ALOX15 P16050 1/20 0.37
SMN1; SMN2 Q16637 1/20 0.36
TSHR P16473 3/20 0.36
MAPK1 P28482 1/20 0.35
KMT2A Q03164 2/20 0.35
MAPT P10636 1/20 0.35
MEN1 O00255 1/20 0.35
GAA P10253 1/20 0.35
PKM P14618 1/20 0.35
PGK1 P00558 1/20 0.34
PGK2 P07205 1/20 0.34
KCNN4 O15554 1/20 0.34
CYP2C9 P11712 1/20 0.34
LMNA P02545 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
Inositol SCHEMBL8443504 0.94 TAAR1 (0.37) TAAR1PTPN1POLBCYP2C19HIF1A
Phosphoric Acid SCHEMBL5665038 0.90 TAAR1 (0.41) TAAR1PTPN1POLBCYP2C19HIF1A
SCHEMBL55578 0.89 TAAR1 (0.50) TAAR1CYP2C19HIF1AALDH1A1ALOX15
Phosphine SCHEMBL9467574 0.87 TAAR1 (0.48) TAAR1CYP2C19HIF1AALDH1A1ALOX15
SCHEMBL9144235 0.87 TAAR1 (0.48) TAAR1CYP2C19HIF1AALDH1A1ALOX15
Iodide SCHEMBL6625841 0.87 TAAR1 (0.48) TAAR1CYP2C19HIF1AALDH1A1ALOX15
Sulfuric Acid SCHEMBL9177660 0.86 TAAR1 (0.41) TAAR1CYP2C19HIF1AALDH1A1ALOX15
Acetic Acid SCHEMBL3397599 0.86 CYP2C19 (0.42) TAAR1CYP2C19HIF1AALDH1A1ALOX15
Inositol SCHEMBL3079466 0.84 TAAR1 (0.42) TAAR1CYP2C19HIF1AALDH1A1ALOX15
SCHEMBL1659303 0.83 ITPR3 (0.40)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2004085638-A1 PHYTASE PRODUCED FROM CITROBACTER BRAAKII REPUBLIC OF NATIONAL FISHERIES RESEARCH AND DEVELOPMENT INSTITUTE (KR) 2004-10-07 WO disclosed
EP-1170994-A1 TRANSGENIC ANIMALS EXPRESSING SALIVARY PROTEINS UNIVERSITY OF GUELPH (CA) 2002-01-16 EP disclosed
WO-2000064247-A1 TRANSGENIC ANIMALS EXPRESSING SALIVARY PROTEINS UNIVERSITY OF GUELPH (CA) 2000-11-02 WO disclosed
WO-1997021729-A9 METHODS AND COMPOSITIONS FOR MODULATING VESICLE RELEASE 1997-11-06 WO disclosed
WO-1997021729-A1 METHODS AND COMPOSITIONS FOR MODULATING VESICLE RELEASE SLOAN-KETTERING INSTITUTE FOR CANCER RESEARCH (US) 1997-06-19 WO disclosed
US-5434144-A Methods of using cyclic polyanionic polyol derivatives for regulating skin wrinkles THE PROCTER & GAMBLE COMPANY (US) 1995-07-18 US disclosed