3-Methylbutanol

3-Methylbutanol

SCHEMBL11364355

CC(C)CCO.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.45

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of 3-Methylbutanol. 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
CYP2C19 P33261 3/20 0.45
CYP1A2 P05177 3/20 0.45
ALDH1A1 P00352 4/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
LMNA P02545 2/20 0.44
KDM4E B2RXH2 1/20 0.44
MAPT P10636 1/20 0.44
HTT P42858 1/20 0.44
TDP1 Q9NUW8 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
CYP2D6 P10635 3/20 0.44
CYP3A4 P08684 2/20 0.44
ALOX15 P16050 1/20 0.44
GBA1 P04062 1/20 0.44
MEN1 O00255 1/20 0.43
KMT2A Q03164 1/20 0.43
MAPK1 P28482 1/20 0.43
CA2 P00918 2/20 0.42
CA12 O43570 1/20 0.42
CA9 Q16790 1/20 0.42

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
1,3-Butanediol SCHEMBL9484102 0.88 ALDH1A1 (0.43) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
SCHEMBL11363256 0.88 PSEN1 (0.41) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Isobutanol SCHEMBL28032479 0.87 ALDH1A1 (0.47) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
3-Methylbutanol SCHEMBL28329624 0.86 CYP1A2 (0.40) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
SCHEMBL31476892 0.85 CA2 (0.43) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Ethylene Glycol SCHEMBL1936216 0.85 GAA (0.52) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Ethylene Glycol SCHEMBL6046435 0.85 GAA (0.52) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Ethylene Glycol SCHEMBL6046494 0.85 GAA (0.52) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Ethylene Glycol SCHEMBL1247518 0.85 GAA (0.52) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA
Ethylene Glycol SCHEMBL3283790 0.85 GAA (0.52) CYP2C19CYP1A2ALDH1A1SMN1; SMN2LMNA

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
US-4305876-A CULTURE PRODUCT INTERMEDIATE IN THE PREPARATION OF VITAMINS E AND K HOFFMANN-LA ROCHE, INC. (US) 1981-12-15 US disclosed
US-4138289-A ASYMMETRIC HYDROGENATION BY MICROORGANISM, FERMENTATION HOFFMANN-LA ROCHE INC. (US) 1979-02-06 US disclosed