Phosphoric Acid

Phosphoric Acid

SCHEMBL28049090

CCCCCCCC/C=C\CCCCCCCC(=O)[N+](C)(C)C.CCCCCCCC/C=C\CCCCCCCC(=O)[N+](C)(C)C.CCCCCCCC/C=C\CCCCCCCC(=O)[N+](C)(C)C.O=P([O-])([O-])[O-]

nearest known ligand 0.62

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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
KCNH2 known ✓ Q12809 1/20 0.56
FABP3 P05413 6/20 0.62
TERT O14746 3/20 0.56
PTPN1 P18031 3/20 0.56
PPARG P37231 3/20 0.56
PPARD Q03181 3/20 0.56
PPARA Q07869 3/20 0.56
FAAH O00519 3/20 0.56
CYP1A2 P05177 2/20 0.56
MAPT P10636 2/20 0.56
CYP2C19 P33261 2/20 0.56
BLM P54132 2/20 0.56
HSD17B10 Q99714 2/20 0.56
FABP4 P15090 2/20 0.56
KMT2A Q03164 2/20 0.56
GMNN O75496 1/20 0.56
USP2 O75604 1/20 0.56
LMNA P02545 1/20 0.56
POLB P06746 1/20 0.56
CYP2C9 P11712 1/20 0.56

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
Phosphoric Acid SCHEMBL28049093 0.93 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
SCHEMBL4047249 0.93 FABP3 (0.65) FABP3TERTPTPN1PPARGPPARD
SCHEMBL27509400 0.93 FABP3 (0.65) FABP3TERTPTPN1PPARGPPARD
SCHEMBL157762 0.93 FABP3 (0.65) FABP3TERTPTPN1PPARGPPARD
Bromide SCHEMBL23798635 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
Iodide SCHEMBL9324294 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
Hydrochloric Acid SCHEMBL1029165 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
Hydrochloric Acid SCHEMBL6940059 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
Fluoride Ion SCHEMBL29227705 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD
Water SCHEMBL8017014 0.91 FABP3 (0.62) FABP3TERTPTPN1PPARGPPARD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105163762-A Treatment for exposure to nerve agent UNIV GEORGETOWN 2015-12-16 CN claimed
CN-109312341-A micro-RNAs and methods of use thereof 美国政府(由卫生和人类服务部的部长所代表) 2019-02-05 CN disclosed
CN-105163762-A Treatment for exposure to nerve agent UNIV GEORGETOWN 2015-12-16 CN disclosed