Valeric Acid

Valeric Acid

SCHEMBL29627993

CCCCC(=O)[O-].CCCCC(O)C(=O)[O-].[Na+].[Na+]

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Valeric Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
CA1 known ✓ P00915 2/20 0.65
CA2 known ✓ P00918 4/20 0.55
CA4 known ✓ P22748 1/20 0.43
NFKB1 P19838 1/20 0.59
GPR84 Q9NQS5 1/20 0.53
FFAR3 O14843 2/20 0.46
HDAC3 O15379 2/20 0.46
HDAC1 Q13547 2/20 0.46
HDAC2 Q92769 2/20 0.46
HDAC8 Q9BY41 2/20 0.46
FABP3 P05413 2/20 0.43
CES2 O00748 1/20 0.43
CES1 P23141 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
SCHEMBL28427993 0.90 CA2 (0.59) CA1NFKB1CA2GPR84CA4
SCHEMBL30463176 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL29800285 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL2483933 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL6535441 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL29572976 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL6865427 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
Potassium Ion SCHEMBL29800416 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
SCHEMBL31257325 0.86 CA2 (0.54) CA1NFKB1CA2GPR84CA4
Ammonia Solution, Strong SCHEMBL8757949 0.84 CA2 (0.52) CA1NFKB1CA2GPR84CA4

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-111437617-B Method and equipment for evaporating and concentrating cyclohexane oxidation waste alkali liquor 长沙兴和新材料有限公司 2022-05-03 CN disclosed