Phosphoric Acid

Phosphoric Acid

SCHEMBL3301227

C/C(=C\CNc1ncnc2[nH]cnc12)CO.O=P(O)(O)O

nearest known ligand 0.59

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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 16)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 2/20 0.59
▸ RECQL P46063 1/20 0.59
▸ CYP1A2 P05177 2/20 0.44
▸ CDK2 P24941 1/20 0.44
▸ CCNB2 O95067 2/20 0.39
▸ CDK1 P06493 2/20 0.39
▸ CCNB1 P14635 2/20 0.39
▸ CCNB3 Q8WWL7 2/20 0.39
▸ AHCY P23526 2/20 0.33
▸ TP53 P04637 1/20 0.32
▸ HSD17B10 Q99714 1/20 0.32
▸ CYP3A4 P08684 1/20 0.32
▸ BTN3A1 O00481 1/20 0.31
▸ HIF1A Q16665 1/20 0.31
▸ ENPP1 P22413 1/20 0.30
▸ BRAF P15056 1/20 0.30

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
SCHEMBL15950878 0.94 TSHR (0.66) TSHRRECQLCYP1A2CDK2CCNB2
SCHEMBL49689 0.94 TSHR (0.66) TSHRRECQLCYP1A2CDK2CCNB2
SCHEMBL14876945 0.94 TSHR (0.66) TSHRRECQLCYP1A2CDK2CCNB2
Hydrochloric Acid SCHEMBL584648 0.92 TSHR (0.64) TSHRRECQLCYP1A2CDK2CCNB2
SCHEMBL17693471 0.83 TSHR (0.52) TSHRRECQLCYP1A2CDK2CCNB2
SCHEMBL17693470 0.83 TSHR (0.52) TSHRRECQLCYP1A2CDK2CCNB2
Phosphoric Acid SCHEMBL29264659 0.82 TSHR (0.88) TSHRRECQLCYP1A2CDK2TP53
Phosphoric Acid SCHEMBL3301229 0.82 TSHR (0.88) TSHRRECQLCYP1A2CDK2TP53
Xylose SCHEMBL3866081 0.82 TSHR (0.50) TSHRRECQLCYP1A2CDK2CCNB2
SCHEMBL2027216 0.82 CDK2 (0.63) TSHRRECQLCYP1A2CDK2CCNB2

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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