Cetyl Alcohol

Cetyl Alcohol

SCHEMBL28774331

C1CO1.CCCCCCCCCCCCCCCCO.O

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABCC9ABL1ACEACHEACVR1ADORA1ADORA2AADORA2BADORA3ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALOX5ATP4AATP4BBCRBTKCACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGCRBNCUL4ACXCR1CXCR2DDB1DDCDHFRDPP4DRD2DRD3DRD4EGFRERBB2ERBB4ESR1ESR2FDPSFKBP1AFLT1FLT3FLT4GARTGHSRGRIA1GRIA2GRIA3GRIA4GRIK1GRIK2GRIK3GRIK4GRIK5GRIN2AGSK3AGSK3BHDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IDH1IDH2IMPA1ITGA2BITGB3JAK1JAK2JAK3KCNJ11KCNK3KCNK9KDRKITMEN1METMMP1MMP13MMP7MMP8NANOD2NS5bODC1OPG057OPRD1OPRK1OPRM1PPARP1PARP2PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PKLRPPARDPPATPTGS1PTGS2RBX1ROCK1ROCK2RRM1RRM2RRM2BSCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC10A2SLC5A2SLC6A2SLC6A3SLC6A4SLC9A3SYKTACR1THRATHRBTOP1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYK2TYMSVDRampCblablaT-3blaT-4blaT-5blaT-6blaUOE-1dacAdacBdacCfolAfolPftsIgyrAgyrBileSmecAmrcAmrcBmrdAparCparEpbp2pbp4pbpApbpFrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUthyAykgMykgO

The experimentally established mechanism targets of Cetyl Alcohol. 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
MEN1 known ✓ O00255 2/20 0.68
THRB known ✓ P10828 2/20 0.42
LMNA P02545 3/20 0.68
ALDH1A1 P00352 3/20 0.68
TSHR P16473 2/20 0.68
KMT2A Q03164 2/20 0.68
HSD17B10 Q99714 1/20 0.68
SMN1; SMN2 Q16637 1/20 0.63
DNM1 Q05193 2/20 0.39
HTT P42858 1/20 0.39
MAPT P10636 1/20 0.39
EPHX1 P07099 1/20 0.38
CES2 O00748 3/20 0.35
CES1 P23141 3/20 0.35

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
Dodecanol SCHEMBL27709305 1.00 LMNA (0.68) LMNAALDH1A1TSHRMEN1KMT2A
Docosanol SCHEMBL1899631 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Nonanol SCHEMBL8751480 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Decanol SCHEMBL4441171 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Cetostearyl Alcohol SCHEMBL1813578 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Octanol SCHEMBL2321504 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Oxirane SCHEMBL1899535 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Dodecanol SCHEMBL1706785 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Oxirane SCHEMBL1900511 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A
Oxirane SCHEMBL7067127 0.97 LMNA (0.72) LMNAALDH1A1TSHRMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-101227887-B Use of anionically and cationically ampholytic copolymers BASF AG 2011-05-25 CN disclosed
CN-101287441-A Cosmetic preparation for skin BASF SE (DE) 2008-10-15 CN disclosed
CN-101227887-A Use of anionically and cationically ampholytic copolymers BASF AG (DE) 2008-07-23 CN disclosed