Phosphoric Acid

Phosphoric Acid

SCHEMBL31053909

Cc1cc(C)c(O)c(C(C)(C)C)c1.Cc1cc(C)c(O)c(C(C)(C)C)c1.Cc1cc(C)c(O)c(C(C)(C)C)c1.O=P(O)(O)O

nearest known ligand 0.63

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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
SMN1; SMN2 Q16637 3/20 0.63
CA2 P00918 3/20 0.63
ALDH1A1 P00352 3/20 0.63
POLB P06746 1/20 0.63
TYR P14679 1/20 0.63
CYP2C9 P11712 3/20 0.57
CYP2C19 P33261 3/20 0.57
CYP1A2 P05177 1/20 0.57
HSPA5 P11021 1/20 0.52
HIF1A Q16665 2/20 0.50
CYP2D6 P10635 1/20 0.49
HSD17B10 Q99714 1/20 0.49
CA1 P00915 2/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
GALR3 O60755 1/20 0.43
HTT P42858 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
GABRA1 P14867 1/20 0.42
GABRB2 P47870 1/20 0.42

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
SCHEMBL38838 0.90 SMN1; SMN2 (0.77) SMN1; SMN2CA2ALDH1A1POLBTYR
SCHEMBL5318298 0.90 SMN1; SMN2 (0.77) SMN1; SMN2CA2ALDH1A1POLBTYR
SCHEMBL29364506 0.90 SMN1; SMN2 (0.77) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL5514381 0.88 ALDH1A1 (0.82) SMN1; SMN2CA2ALDH1A1POLBTYR
Hydrochloric Acid SCHEMBL10565599 0.88 SMN1; SMN2 (0.74) SMN1; SMN2CA2ALDH1A1POLBTYR
Phosphoric Acid SCHEMBL28263412 0.85 CYP1A2 (0.57) SMN1; SMN2CA2ALDH1A1POLBTYR
Dimethylamine SCHEMBL10449628 0.84 SMN1; SMN2 (0.68) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL9280148 0.82 SMN1; SMN2 (0.72) SMN1; SMN2CA2ALDH1A1POLBTYR
SCHEMBL28584661 0.81 SMN1; SMN2 (0.59) SMN1; SMN2CA2ALDH1A1POLBTYR
Phosphoric Acid SCHEMBL11210498 0.80 HSPA5 (0.83) SMN1; SMN2CA2ALDH1A1POLBTYR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118507126-A High-flame-retardance low-temperature-resistant security fire-proof cable for extremely cold region and production process 浙江光大普特通讯科技股份有限公司 2024-08-16 CN disclosed