Phosphoric Acid

Phosphoric Acid

SCHEMBL28045407

NNc1ccc(Cl)cc1.O=P(O)(O)O

nearest known ligand 0.53

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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
MAPT P10636 5/20 0.48
ALDH1A1 P00352 4/20 0.48
KDM4E B2RXH2 3/20 0.48
NPC1 O15118 3/20 0.48
LMNA P02545 2/20 0.48
L3MBTL1 Q9Y468 1/20 0.48
CA2 P00918 4/20 0.44
CA9 Q16790 3/20 0.44
CA14 Q9ULX7 2/20 0.44
MMP2 P08253 1/20 0.44
MMP9 P14780 1/20 0.44
MMP8 P22894 1/20 0.44
MMP14 P50281 1/20 0.44
PTGS2 P35354 2/20 0.44
CA1 P00915 3/20 0.43
TDP1 Q9NUW8 3/20 0.41
RAB9A P51151 2/20 0.41
POLB P06746 1/20 0.41
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41

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
SCHEMBL7843 0.85
Hydrochloric Acid SCHEMBL73388 0.83 MAPT (0.48) MAPTALDH1A1KDM4ENPC1LMNA
Sulfuric Acid SCHEMBL7599722 0.82 CA1 (0.54) MAPTALDH1A1KDM4ENPC1LMNA
Oxalic Acid SCHEMBL28045429 0.82 NPC1 (0.54) MAPTALDH1A1KDM4ENPC1LMNA
Hydrochloric Acid SCHEMBL1712305 0.80 MAPT (0.46) MAPTALDH1A1KDM4ENPC1LMNA
1,4-Dichlorobenzene SCHEMBL28425304 0.80 LMNA (0.57) MAPTALDH1A1KDM4ELMNAL3MBTL1
Phosphoric Acid SCHEMBL29102150 0.79 CA1 (0.52) MAPTALDH1A1KDM4ENPC1LMNA
Nitric Acid SCHEMBL28280438 0.78 MAPT (0.54) MAPTALDH1A1KDM4ENPC1LMNA
SCHEMBL28375697 0.77 CA1 (0.43) MAPTALDH1A1KDM4ENPC1LMNA
Phosphoric Acid SCHEMBL20985041 0.77 CA12 (0.53) ALDH1A1NPC1LMNACA2CA9

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.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107663160-B A kind of continuous flow synthesis technology of 4- chlorobenzene hydrazonium salt 上海惠和化德生物科技有限公司 2019-03-01 CN claimed
CN-105272875-A 4-chlorophenylhydrazine phosphate preparation method TIANJIN CHEM REAGENT RES INST 2016-01-27 CN claimed
CN-107663160-B A kind of continuous flow synthesis technology of 4- chlorobenzene hydrazonium salt 上海惠和化德生物科技有限公司 2019-03-01 CN disclosed
CN-107663160-A A kind of continuous stream synthesis technique of 4 chlorobenzene hydrazonium salt 上海惠和化德生物科技有限公司 2018-02-06 CN disclosed
CN-105272875-A 4-chlorophenylhydrazine phosphate preparation method TIANJIN CHEM REAGENT RES INST 2016-01-27 CN disclosed
CN-105272875-A 4-chlorophenylhydrazine phosphate preparation method TIANJIN CHEM REAGENT RES INST 2016-01-27 CN disclosed
CN-105272875-A 4-chlorophenylhydrazine phosphate preparation method TIANJIN CHEM REAGENT RES INST 2016-01-27 CN disclosed