Hippuric Acid

Hippuric Acid

SCHEMBL1458080

O=C(O)CNC(=O)c1ccccc1.[LiH]

nearest known ligand 0.66

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Known targets — ChEMBL curated mechanism

TPH1TPH2

The experimentally established mechanism targets of Hippuric 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 2/20 0.66
▸ KDM4E B2RXH2 1/20 0.66
▸ HIF1A Q16665 1/20 0.66
▸ SLC22A6 Q4U2R8 1/20 0.66
▸ SLC22A8 Q8TCC7 1/20 0.66
▸ GAA P10253 1/20 0.65
▸ CA1 P00915 2/20 0.58
▸ CA2 P00918 1/20 0.58
▸ PTPRC P08575 2/20 0.56
▸ CTSL P07711 1/20 0.56
▸ PTPN13 Q12923 1/20 0.56
▸ ATM Q13315 1/20 0.54
▸ NPC1 O15118 4/20 0.53
▸ RAB9A P51151 4/20 0.53
▸ SMN1; SMN2 Q16637 3/20 0.53
▸ LMNA P02545 1/20 0.53
▸ POLB P06746 1/20 0.53
▸ GPR139 Q6DWJ6 1/20 0.53
▸ HDAC3 O15379 1/20 0.52
▸ CA12 O43570 1/20 0.52

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
SCHEMBL22030672 0.98 GAA (0.68) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL7486 0.98 GAA (0.68) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL428479 0.98 GAA (0.68) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL587978 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL21569381 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL11656206 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL7796688 0.96 KDM4E (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL3448563 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL7398337 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8
Hippuric Acid SCHEMBL1179259 0.96 MAPT (0.66) MAPTKDM4EHIF1ASLC22A6SLC22A8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130204238-A1 COMBINATION THERAPY FOLLICA, INC (US) 2013-08-08 — — US disclosed
EP-2552323-A1 COMBINATION THERAPY Follica, Inc. (US) 2013-02-06 — — EP disclosed
WO-2012125941-A1 LITHIUM TREATMENT FOR MICROBIAL INFECTIONS FOLLICA, INC. (US) 2012-09-20 — — WO disclosed
WO-2012067632-A1 SEQUENTIAL BODY SURFACE TREATMENT FOLLICA, INC. (US) 2012-05-24 — — WO disclosed
WO-2012067630-A1 HAIR GROWTH TREATMENT FOLLICA, INC. (US) 2012-05-24 — — WO disclosed
WO-2012067631-A1 BODY SURFACE TREATMENT FOLLICA, INC. (US) 2012-05-24 — — WO disclosed
WO-2011123218-A1 COMBINATION THERAPY FOLLICA, INC. (US) 2011-10-06 — — WO disclosed
US-20110130711-A1 HAIR GROWTH TREATMENT FOLLICA, INC. (US) 2011-06-02 — — US disclosed
US-20110130748-A1 BODY SURFACE TREATMENT FOLLICA, INC. (US) 2011-06-02 — — US disclosed
US-20110130706-A1 SEQUENTIAL BODY SURFACE TREATMENT FOLLICA, INC. (US) 2011-06-02 — — US disclosed
WO-2011031990-A1 INTERMITTENT AND PULSE LITHIUM TREATMENTS FOR MODULATING HAIR GROWTH FOLLICA, INC. (US) 2011-03-17 — — WO disclosed
WO-2011031977-A1 INTERMITTENT AND PULSE LITHIUM TREATMENTS FOR SCAR REVISION AND WOUND HEALING FOLLICA, INC. (US) 2011-03-17 — — WO disclosed
US-6126855-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 2000-10-03 — — US disclosed
US-5833877-A DIAGMAGNETIC COMPLEX; SUPERCONDUCTORS ELLIOTT STANLEY B (US) 1998-11-10 — — US disclosed
US-5595683-A COMPLEX OF METAL SALT OF BENZOYLPROPIONIC ACID, LATTICE MODIFIER, CYCLIZATION, HUMIDITY SENSORS ELLIOTT STANLEY B (US) 1997-01-21 — — US disclosed
US-5443753-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 1995-08-22 — — US disclosed
US-5354499-A Reaction products of lyotropic liquid crystal salt complexes ELLIOTT STANLEY B (US) 1994-10-11 — — US disclosed
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