Phosphoric Acid

Phosphoric Acid

SCHEMBL3301229

CC(=CCNc1ncnc2nc[nH]c12)CO.O=P(O)(O)O

nearest known ligand 0.88

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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
▸ TSHR P16473 3/20 0.88
▸ RECQL P46063 2/20 0.88
▸ CYP1A2 P05177 4/20 0.69
▸ CDK2 P24941 2/20 0.69
▸ CYP3A4 P08684 2/20 0.53
▸ TP53 P04637 1/20 0.51
▸ HSD17B10 Q99714 1/20 0.51
▸ HTT P42858 3/20 0.50
▸ LMNA P02545 2/20 0.50
▸ HIF1A Q16665 1/20 0.49
▸ BRAF P15056 1/20 0.46
▸ PRMT1 Q99873 1/20 0.45
▸ MAPK1 P28482 2/20 0.44
▸ CYP2D6 P10635 1/20 0.44
▸ HDAC1 Q13547 1/20 0.44
▸ HDAC2 Q92769 1/20 0.44
▸ SMN1; SMN2 Q16637 1/20 0.44
▸ NPC1 O15118 1/20 0.43
▸ RAB9A P51151 1/20 0.43
▸ BRD4 O60885 1/20 0.43

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 SCHEMBL29264659 1.00 TSHR (0.88) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL29412055 0.94 TSHR (1.00) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL1944933 0.94 TSHR (1.00) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL29350488 0.94 TSHR (1.00) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL49690 0.94 TSHR (1.00) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL25176316 0.94 TSHR (1.00) TSHRRECQLCYP1A2CDK2CYP3A4
Hydrochloric Acid SCHEMBL584649 0.93 TSHR (0.97) TSHRRECQLCYP1A2CDK2CYP3A4
Hydrochloric Acid SCHEMBL27865862 0.93 TSHR (0.97) TSHRRECQLCYP1A2CDK2CYP3A4
Alcohol SCHEMBL28719125 0.91 TSHR (0.95) TSHRRECQLCYP1A2CDK2CYP3A4
SCHEMBL30320043 0.91 TSHR (0.88) TSHRRECQLCYP1A2CDK2CYP3A4

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
US-7741548-B2 Method and composition for increasing branching and flowering response in plants UNIVERSITY OF CONNECTICUT (US) 2010-06-22 — — US disclosed
US-20070083948-A1 Method and composition for increasing branching and flowering response in plants UNIVERSITY OF CONNECTICUT 2007-04-12 — — US disclosed
EP-0248984-A2 Production of cytokinins by microorganisms THE STATE OF OREGON ACTING BY AND THROUGH THE OREGON STATEBOARD OF HIGHER EDUCATION ON BEHALF OF OREGON STATE UNIVERSITY (US) 1987-12-16 — — EP disclosed
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