Cetostearyl Alcohol

Cetostearyl Alcohol

SCHEMBL2194656

CCCCCCCCCCCCCCCCCCO.Cc1ccc(S(=O)(=O)O)cc1

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1BMXBRAFBTKCHRNA4CHRNB2CSNK1EEGFRERBB2F10FLT1FLT3FLT4IGF1RINSRITKJAK3KDRKITOPRM1PARP1PARP2PDGFRBPIK3CDRAF1RETSLC18A2TECTXKdacAdacBdacCftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Cetostearyl Alcohol. 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
MCHR1 Q99705 1/20 0.50
ALDH1A1 P00352 6/20 0.49
L3MBTL1 Q9Y468 2/20 0.45
LMNA P02545 4/20 0.45
TSHR P16473 2/20 0.45
HSD17B10 Q99714 1/20 0.45
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45
CYP2C9 P11712 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
ALB P02768 1/20 0.44
S1PR3 Q99500 1/20 0.43
SMN1; SMN2 Q16637 4/20 0.43
CYP3A4 P08684 1/20 0.43
CYP2C19 P33261 1/20 0.43
CNR2 P34972 1/20 0.43
KDM4E B2RXH2 1/20 0.43
MAPT P10636 1/20 0.43
HTT P42858 1/20 0.43
RECQL P46063 1/20 0.41

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
Cetyl Alcohol SCHEMBL27625313 1.00 MCHR1 (0.50) MCHR1ALDH1A1L3MBTL1LMNATSHR
Octanol SCHEMBL27906975 1.00 MCHR1 (0.50) MCHR1ALDH1A1L3MBTL1LMNATSHR
Decanol SCHEMBL8858135 0.98 MCHR1 (0.49) MCHR1ALDH1A1L3MBTL1LMNATSHR
Butyl Alcohol SCHEMBL9636993 0.93 ALDH1A1 (0.46) MCHR1ALDH1A1L3MBTL1LMNATSHR
1,5-Pentanediol SCHEMBL3465348 0.93 ALDH1A1 (0.48) ALDH1A1L3MBTL1LMNATSHRMEN1
Octane SCHEMBL356741 0.93 MCHR1 (0.56) MCHR1ALDH1A1L3MBTL1LMNATSHR
Heptane SCHEMBL8501523 0.93 MCHR1 (0.56) MCHR1ALDH1A1L3MBTL1LMNATSHR
Octane SCHEMBL8462698 0.93 MCHR1 (0.56) MCHR1ALDH1A1L3MBTL1LMNATSHR
Dodecane SCHEMBL7126605 0.93 MCHR1 (0.56) MCHR1ALDH1A1L3MBTL1LMNATSHR
Nonane SCHEMBL28716314 0.93 MCHR1 (0.56) MCHR1ALDH1A1L3MBTL1LMNATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-219898054-U Drop adding device for batyl alcohol reaction kettle 常州亚邦制药有限公司 2023-10-27 CN disclosed
EP-2524205-A1 ESTIMATION OF RESERVOIR PERMEABILITY General Electric Company (US) 2012-11-21 EP disclosed
US-20110167896-A1 ESTIMATION OF RESERVOIR PERMEABILITY GENERAL ELECTRIC COMPANY (US) 2011-07-14 US disclosed
WO-2011084656-A1 ESTIMATION OF RESERVOIR PERMEABILITY GENERAL ELECTRIC COMPANY (US) 2011-07-14 WO disclosed
CN-101024601-A Novel method for industrially producing batyl alcohol ZHANG GUOTAO (CN) 2007-08-29 CN disclosed