Phosphoric Acid

Phosphoric Acid

SCHEMBL30728570

O=P(O)(O)O.O=c1[nH]c(=O)c2ncn([C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)c2[nH]1

nearest known ligand 0.65

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Known targets — ChEMBL curated mechanism

ADRA1AADRA1BADRA1DADRB1ADRB2ADRB3CYP11B1DPP4FGFR1FGFR2FGFR3FGFR4HRH1JAK1JAK2JAK3KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITNAOPRD1OPRK1OPRM1PPDGFRBPIK3CDSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASMOTYK2polrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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
▸ ADRB2 known ✓ P07550 1/20 0.57
▸ KCNH2 known ✓ Q12809 1/20 0.57
▸ IMPDH2 P12268 7/20 0.65
▸ IMPDH1 P20839 2/20 0.65
▸ TAS1R3 Q7RTX0 3/20 0.61
▸ TAS1R1 Q7RTX1 3/20 0.61
▸ DNPH1 O43598 3/20 0.57
▸ FBP1 P09467 2/20 0.57
▸ PRKAB2 O43741 1/20 0.57
▸ TRPM2 O94759 1/20 0.57
▸ LDHA P00338 1/20 0.57
▸ SRC P12931 1/20 0.57
▸ ADORA1 P30542 1/20 0.57
▸ P2RY2 P41231 1/20 0.57
▸ P2RY1 P47900 1/20 0.57
▸ PRKAG1 P54619 1/20 0.57
▸ PRKAA2 P54646 1/20 0.57
▸ PDE4D Q08499 1/20 0.57
▸ PRKAA1 Q13131 1/20 0.57
▸ PDE3A Q14432 1/20 0.57

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
SCHEMBL22986473 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL4356337 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL27862445 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL188741 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL188739 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL12727828 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL2217345 0.99 IMPDH2 (0.66) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL22635931 0.98 IMPDH2 (0.65) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL20266268 0.98 IMPDH2 (0.65) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1
SCHEMBL28340155 0.98 IMPDH2 (0.65) IMPDH2IMPDH1TAS1R3TAS1R1DNPH1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112210522-B Microorganism of corynebacterium genus producing 5 '-xanthosine-monophosphate and method for producing 5' -xanthosine-monophosphate using the same CJ第一制糖株式会社 2024-01-05 — — CN disclosed
CN-112210522-B Microorganism of corynebacterium genus producing 5 '-xanthosine-monophosphate and method for producing 5' -xanthosine-monophosphate using the same CJ第一制糖株式会社 2024-01-05 — — CN disclosed
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