Hexadecylamine

Hexadecylamine

SCHEMBL8712148

CC(C)C.CCCCCCCCCCCCCCCCN.Cl

nearest known ligand 0.82

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ACEACHEACVR1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3AGTR1ALKAVPR1AAVPR2BCHEBCRCA2CACNA1ACACNA1BCACNA1CCACNA1DCACNA1ECACNA1FCACNA1GCACNA1HCACNA1ICACNA1SCACNA2D1CACNA2D2CACNA2D3CACNA2D4CACNB1CACNB2CACNB3CACNB4CACNG1CACNG2CACNG3CACNG4CACNG5CACNG6CACNG7CACNG8CALCRLCASRCCR5CDK4CDK6CFBCHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNA3CHRNA7CHRNB1CHRNB4CHRNDCHRNECHRNGCOXFA4COXFA4L2CRBNCSF1RCUL4ACYP19A1DDB1DPP4DRD1DRD2DRD3DRD4EDNRAEGFREML4ERBB2ERBB4ESR1ESR2FGFR1FGFR3FLT1FLT3FLT4GAAGABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGHSRGLAGNRHRGPD2GRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BGSTP1HCN4HCRTR1HCRTR2HDAC1HDAC10HDAC11HDAC2HDAC3HDAC4HDAC5HDAC6HDAC7HDAC8HDAC9HRH1HRH2HRH3HSD11B1HSP90AA1HSP90AB1HTR1AHTR1BHTR1DHTR1EHTR1FHTR2AHTR2BHTR2CHTR3AHTR3BHTR3CHTR3DHTR3EHTR4HTR5AHTR6HTR7IMPDH1IMPDH2ITGA2BITGB3ITKJAK1JAK2KCNA1KCNA10KCNA2KCNA3KCNA4KCNA5KCNA6KCNA7KCNB1KCNB2KCNC1KCNC2KCNC3KCNC4KCND1KCND2KCND3KCNF1KCNG1KCNG2KCNG3KCNG4KCNH1KCNH2KCNH3KCNH4KCNH5KCNH6KCNH7KCNH8KCNJ2KCNJ3KCNJ5KCNK3KCNK9KCNQ1KCNQ2KCNQ3KCNQ4KCNQ5KCNS1KCNS2KCNS3KCNV1KCNV2KDRKITKLKB1LCKMMAOAMAOBMAPK14METMMP1MMP13MMP7MMP8MT-ND1MT-ND2MT-ND3MT-ND4MT-ND4LMT-ND5MT-ND6NDUFA1NDUFA10NDUFA11NDUFA12NDUFA13NDUFA2NDUFA3NDUFA5NDUFA6NDUFA7NDUFA8NDUFA9NDUFAB1NDUFAF1NDUFAF2NDUFAF3NDUFAF4NDUFB1NDUFB10NDUFB11NDUFB2NDUFB3NDUFB4NDUFB5NDUFB6NDUFB7NDUFB8NDUFB9NDUFC1NDUFC2NDUFS1NDUFS2NDUFS3NDUFS4NDUFS5NDUFS6NDUFS7NDUFS8NDUFV1NDUFV2NDUFV3NR3C1NS5ANTRK1NTRK2NTRK3ODC1OPRD1OPRK1OPRM1P2RY12PAHPARP1PDE3APDE3BPDE4APDE4BPDE4CPDE4DPDE5APDE7APDE7BPDE8APDE8BPDGFRAPDGFRBPIK3CAPIK3CDPNPPOLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PPARGPRIM1PRIM2PRKCAPRKCBPRKCDPRKCEPRKCGPRKCHPRKCIPRKCQPRKCZPRKD1PRKD3PTGS1PTGS2RBX1RENRETROCK1ROCK2RPE65RRM1RRM2RRM2BS1PR1S1PR2S1PR3S1PR4S1PR5SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASCNN1ASCNN1BSCNN1GSIGMAR1SLC18A2SLC6A1SLC6A2SLC6A3SLC6A4SLC9A3SRCTACR1TOP1TOP2ATOP2BTTRTYMPdacAdacBdacCembAfolAftsIgyrAgyrBmrcAmrcBmrdAparCparEpolrplArplBrplCrplDrplErplFrplIrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmE2rpmFrpmGrpmG1rpmG2rpmG3rpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Hexadecylamine. 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
CA2 known ✓ P00918 2/20 0.47
DNM1 Q05193 9/20 0.82
TSHR P16473 3/20 0.77
MEN1 O00255 1/20 0.77
KMT2A Q03164 1/20 0.77
ALDH1A1 P00352 1/20 0.77
EPHX1 P07099 1/20 0.77
CA12 O43570 2/20 0.47
CA1 P00915 2/20 0.47
CA3 P07451 2/20 0.47
CA4 P22748 2/20 0.47
CA6 P23280 2/20 0.47
CA5A P35218 2/20 0.47
CA7 P43166 2/20 0.47
CA9 Q16790 2/20 0.47
CA14 Q9ULX7 2/20 0.47
CA5B Q9Y2D0 2/20 0.47
THRB P10828 1/20 0.47
LMNA P02545 1/20 0.47
BLM P54132 1/20 0.47

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
Dodecylamine SCHEMBL6675464 1.00 DNM1 (0.82) DNM1TSHRMEN1KMT2AALDH1A1
Hexadecylamine SCHEMBL8855049 0.97 DNM1 (0.81) DNM1TSHRMEN1KMT2AALDH1A1
Isobutane SCHEMBL27489263 0.97 DNM1 (0.77) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL374326 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Octadecylamine SCHEMBL22436608 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL23420707 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Octadecylamine SCHEMBL22436607 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL21494288 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Hydrochloric Acid SCHEMBL608566 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1
Dodecylamine SCHEMBL7791999 0.91 DNM1 (1.00) DNM1TSHRMEN1KMT2AALDH1A1

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 28 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5008345-A Two-Part Curing System Containing A Metallic Acid Salt And An Ammonium Or Phosphonium Quaternary Salt ZEON CHEMICAL USA, INC. (US) 1991-04-16 US claimed
EP-3483194-A1 METHOD FOR PREPARING POLYURETHANE RESIN AND POLYURETHANE RESIN PREPARED THEREBY Covestro Deutschland AG (DE) 2019-05-15 EP disclosed
US-9733394-B2 Method for preparing optical lenses COVESTRO DEUTSCHLAND AG (DE) 2017-08-15 US disclosed
US-9718916-B2 Lightfast polyurethane compositions COVESTRO DEUTSCHLAND AG (DE) 2017-08-01 US disclosed
US-9353209-B2 Lightfast polyurethane compositions COVESTRO DEUTSCHLAND AG (DE) 2016-05-31 US disclosed
US-9354355-B2 Lightfast polyurethane composition COVESTRO DEUTSCHLAND AG (DE) 2016-05-31 US disclosed
US-20160139301-A1 Method for Preparing Optical Lenses COVESTRO DEUTSCHLAND AG (DE) 2016-05-19 US disclosed
US-20160137840-A1 LIGHTFAST POLYURETHANE COMPOSITIONS COVESTRO DEUTSCHLAND AG (DE) 2016-05-19 US disclosed
US-20150119546-A1 LIGHTFAST POLYURETHANE COMPOSITIONS COVESTRO DEUTSCHLAND AG (DE) 2015-04-30 US disclosed
US-20150087774-A1 LIGHTFAST POLYURETHANE COMPOSITION COVESTRO DEUTSCHLAND AG (DE) 2015-03-26 US disclosed
US-5081194-A Quaternary ammonium or phosphonium curing agent ZEON CHEMICALS U.S.A., INC. (US) 1992-01-14 US disclosed
US-5079304-A Curable ZEON CHEMICALS U.S.A., INC. (US) 1992-01-07 US disclosed
US-5008345-A Two-Part Curing System Containing A Metallic Acid Salt And An Ammonium Or Phosphonium Quaternary Salt ZEON CHEMICAL USA, INC. (US) 1991-04-16 US disclosed
EP-0374258-A1 HIGH REFRACTIVE INDEX LENS AND METHOD FOR ITS PRODUCTION MITSUI CHEMICALS, INC. (JP) 1990-06-27 EP disclosed
US-4929707-A Polyurethane base lens resin, plastic lens comprising the resin and preparation method of the lens MITSUI TOATSU CHEMICALS, INC. (JP) 1990-05-29 US disclosed
EP-0362459-A1 Polyacrylate polymers utilizing substituted urea retarder Zeon Chemicals USA, Inc. (US) 1990-04-11 EP disclosed
EP-0351073-A2 Lens comprising a resin having a large refractive index and process for preparing the lens MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-01-17 EP disclosed
EP-0329389-A2 Polyurethane base lens and its preparation method MITSUI TOATSU CHEMICALS, Inc. (JP) 1989-08-23 EP disclosed
EP-0309794-A2 No-post-cure method of curing polyacrylate polymers Zeon Chemicals USA, Inc. (US) 1989-04-05 EP disclosed
EP-0271839-A2 Casting polymerisation process for preparing sulfur-containing urethane resin lens MITSUI TOATSU CHEMICALS, Inc. (JP) 1988-06-22 EP disclosed