SCHEMBL9720326

SCHEMBL9720326

CCC(C)C(C(=O)[O-])C(C)(O)c1cccnc1.[Na+]

nearest known ligand 0.42

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CYP3A4 P08684 2/20 0.42
LMNA P02545 1/20 0.42
CYP1A2 P05177 1/20 0.42
CYP11B1 P15538 1/20 0.42
CYP11B2 P19099 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
KCNA5 P22460 2/20 0.39
CYP19A1 P11511 4/20 0.38
NPC1 O15118 2/20 0.38
RAB9A P51151 2/20 0.38
MEN1 O00255 1/20 0.38
KMT2A Q03164 1/20 0.38
CYP3A5 P20815 1/20 0.38
ALDH1A1 P00352 1/20 0.37

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
SCHEMBL9720309 0.87 CYP3A4 (0.43) CYP3A4LMNACYP1A2CYP11B1CYP11B2
Ammonia Solution, Strong SCHEMBL9720294 0.86 CYP3A4 (0.43) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL9720319 0.84 CYP19A1 (0.33) LMNACYP19A1MEN1KMT2A
SCHEMBL9466966 0.84 CYP3A4 (0.41) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL9720329 0.78 KCNA5 (0.47) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL9720347 0.78 CYP19A1 (0.35) LMNACYP19A1NPC1RAB9AKMT2A
Piperidine SCHEMBL9720304 0.78 KCNA5 (0.40) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL9720305 0.76 KCNA5 (0.40) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL12238648 0.72 CYP3A4 (0.49) CYP3A4LMNACYP1A2CYP11B1CYP11B2
SCHEMBL9494010 0.72 KCNA5 (0.49) CYP3A4LMNACYP1A2CYP11B1CYP11B2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5148817-A Heterocyclic hydroxy-substituted carboxylic compound as flavor additive PHILIP MORRIS INCORPORATED (US) 1992-09-22 US claimed
US-5148817-A Heterocyclic hydroxy-substituted carboxylic compound as flavor additive PHILIP MORRIS INCORPORATED (US) 1992-09-22 US disclosed
US-4592373-A Smoking compositions PHILIP MORRIS INC. (US) 1986-06-03 US disclosed
EP-0052969-A2 Flavorant compounds, their pyrolysis products, and smoking and food compositions containing them PHILIP MORRIS INCORPORATED (US) 1982-06-02 EP disclosed