Demannose

Demannose

SCHEMBL4091029

CC(=O)C(C)O.CC(=O)O.CC(C)=O.CCCC(=O)O.CCCCO.CCO.O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO

nearest known ligand 0.36

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

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

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
FPR2 P25090 2/20 0.34
NFKB1 P19838 1/20 0.34
NFKB2 Q00653 1/20 0.34
RELA Q04206 1/20 0.34
FFAR3 O14843 1/20 0.32
HDAC3 O15379 1/20 0.32
HDAC1 Q13547 1/20 0.32
HDAC2 Q92769 1/20 0.32
HDAC8 Q9BY41 1/20 0.32
PDE4A P27815 1/20 0.30
FFAR4 Q5NUL3 1/20 0.30
FFAR1 O14842 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
Butyric Acid SCHEMBL4091036 0.88 PRKCA (0.31) FPR2NFKB1NFKB2RELA
Demannose SCHEMBL27882113 0.85 LMNA (0.37) FPR2NFKB1NFKB2RELAPDE4A
Demannose SCHEMBL28531529 0.85 FFAR3 (0.43) FPR2NFKB1NFKB2RELAFFAR3
Demannose SCHEMBL5586151 0.84 FFAR3 (0.45) FPR2NFKB1NFKB2RELAFFAR3
Demannose SCHEMBL27660938 0.84 FFAR3 (0.45) FPR2NFKB1NFKB2RELAFFAR3
Demannose SCHEMBL18141631 0.81 FPR2 (0.44) FPR2NFKB1NFKB2RELAPDE4A
Demannose SCHEMBL28742780 0.81 FPR2 (0.44) FPR2NFKB1NFKB2RELAPDE4A
Demannose SCHEMBL30163433 0.81 FPR2 (0.44) FPR2NFKB1NFKB2RELAPDE4A
Lactic Acid SCHEMBL18423690 0.81 FFAR3 (0.42) FFAR3HDAC3HDAC1HDAC2HDAC8
Demannose SCHEMBL20765370 0.81 LMNA (0.41) PDE4A

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
EP-2102351-A1 METHOD FOR PREPARING BUTANOL THROUGH BUTYRYL-COA AS AN INTERMEDIATE USING BACTERIA Biofuelchem Co., Ltd. (KR) 2009-09-23 EP disclosed
WO-2008072920-A1 METHOD FOR PREPARING BUTANOL THROUGH BUTYRYL-COA AS AN INTERMEDIATE USING BACTERIA BIOFUELCHEM CO., LTD. (KR) 2008-06-19 WO disclosed