Palmitoyl-Carnitine

Palmitoyl-Carnitine

SCHEMBL527281

CCCCCCCCCCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C.Cl

nearest known ligand 0.97

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 Palmitoyl-Carnitine. 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
HSP90AA1 known ✓ P07900 2/20 0.74
GLA known ✓ P06280 1/20 0.72
HRH1 known ✓ P35367 1/20 0.56
MAPT P10636 5/20 0.97
MEN1 O00255 5/20 0.97
KMT2A Q03164 5/20 0.97
SLC25A20 O43772 3/20 0.97
TP53 P04637 3/20 0.97
TSHR P16473 3/20 0.97
CYP2D6 P10635 2/20 0.97
SLC6A5 Q9Y345 2/20 0.97
CYP2C9 P11712 2/20 0.97
HIF1A Q16665 2/20 0.97
CYP2C19 P33261 2/20 0.97
KDM4E B2RXH2 1/20 0.97
CYP3A4 P08684 1/20 0.97
NFKB1 P19838 1/20 0.97
THPO P40225 1/20 0.97
HSD17B10 Q99714 1/20 0.97
MAPK1 P28482 5/20 0.74

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
Hydrochloric Acid SCHEMBL5499648 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Octanoylcarnitine SCHEMBL2784153 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL1332594 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL307401 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL6676390 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL1332983 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Palmitoyl-Carnitine SCHEMBL2785481 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL6658904 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Hydrochloric Acid SCHEMBL17395722 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53
Octanoylcarnitine SCHEMBL2787592 1.00 MAPT (0.97) MAPTMEN1KMT2ASLC25A20TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260007619-A1 Sublingual Epinephrine Compositions Including pH-Modifying Excipients And Penetration Enhancers And Methods for Use Thereof NOVA SOUTHEASTERN UNIVERSITY (US) 2026-01-08 US claimed
US-20260007622-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE UNIV FLORIDA STATE RES FOUND (US) 2026-01-08 US claimed
EP-4651897-A1 PERMEATION ENHANCERS FOR GASTROINTESTINAL SYNTHETIC EPITHELIAL LININGS Syntis Bio, Inc. (US) 2025-11-26 EP claimed
US-12357591-B2 Sublingual epinephrine compositions including pH-modifying excipients and penetration enhancers and methods for use thereof NOVA SOUTHEASTERN UNIVERSITY (US) 2025-07-15 US claimed
US-20250041253-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. 2025-02-06 US claimed
US-20240261411-A1 PERMEATION ENHANCERS FOR GASTROINTESTINAL SYNTHETIC EPITHELIAL LININGS SYNTIS BIO, INC. 2024-08-08 US claimed
WO-2024155958-A1 PERMEATION ENHANCERS FOR GASTROINTESTINAL SYNTHETIC EPITHELIAL LININGS SYNTIS BIO, INC. (US) 2024-07-25 WO claimed
US-20230390225-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. 2023-12-07 US claimed
CN-114076701-A Dried blood spot quality control product for newborn screening and preparation method thereof 上海安谱实验科技股份有限公司 2022-02-22 CN claimed
US-20220000806-A1 Sublingual Epinephrine Compositions Including pH-Modifying Excipients And Penetration Enhancers And Methods for Use Thereof NOVA SOUTHEASTERN UNIVERSITY (US) 2022-01-06 US claimed
US-20140072627-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS ALA WAI PHARMA, INC. (US) 2014-03-13 US claimed
US-8609139-B2 Formulations for enhanced bioavailability of orally administered polar agents ALA WAI PHARMA, INC. (US) 2013-12-17 US claimed
US-20110206764-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS UNIVERSITY OF HAWAII 2011-08-25 US claimed
EP-2217216-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS Scolr Pharma, Inc. (US) 2010-08-18 EP claimed
WO-2009061805-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS SCOLR PHARMA, INC. (US) 2009-05-14 WO claimed
EP-1225916-A1 COMPOSITIONS AND METHODS FOR CONTROLLED-RELEASE DELIVERY AND INCREASED POTENCY OF PHARMACEUTICALS VIA HYDROPHOBIC ION-PAIRING University Technology Corporation (US) 2002-07-31 EP claimed
WO-2001032218-A1 COMPOSITIONS AND METHODS FOR CONTROLLED-RELEASE DELIVERY AND INCREASED POTENCY OF PHARMACEUTICALS VIA HYDROPHOBIC ION-PAIRING UNIVERSITY TECHNOLOGY CORPORATION (US) 2001-05-10 WO claimed
WO-1999041984-A9 INTERACTION BETWEEN THE MEC1-DEPENDENT DNA SYNTHESIS CHECKPOINT AND G1 CYCLIN FUNCTION IN $i(SACCAROMYCES CEREVISIAE) HUTCHINSON FRED CANCER RES (US) 1999-11-04 WO claimed
WO-1999041984-A1 INTERACTION BETWEEN THE MEC1-DEPENDENT DNA SYNTHESIS CHECKPOINT AND G1 CYCLIN FUNCTION IN $i(SACCAROMYCES CEREVISIAE) FRED HUTCHINSON CANCER RESEARCH CENTER (US) 1999-08-26 WO claimed
US-5525596-A (R-(R*,R*))-3-((2-HYDROXYPROPYL)AMINO)-3-METHYL-N-2,3,4,5-TET RAHYDRO-2-OXO-1-((2'-(H-TETRAZOL-5-YL)(1,1'-BIPHENYL)-4-YL)ME THYL-1H-1-BENZAZEPIN-3-YL)BUTANAMIDE, PALMITOYL CARNITINE AND CYCLODEXTRIN MERCK & CO., INC. (US) 1996-06-11 US claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20250041253-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE TMPRSS2, NCSTN, PRSS2 HSP90AA1 4593/4885GLA 3075/4885HRH1 1844/4885
US-20240261411-A1 PERMEATION ENHANCERS FOR GASTROINTESTINAL SYNTHETIC EPITHELIAL LININGS FABP2, SLC10A2, FABP6 HSP90AA1 2150/4885GLA 640/4885HRH1 438/4885
US-20230390225-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE TMPRSS2, NCSTN, PRSS2 HSP90AA1 4593/4885GLA 3075/4885HRH1 1844/4885
US-20260007622-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE TMPRSS2, PKD2, DSP HSP90AA1 4708/4885GLA 3301/4885HRH1 1580/4885
US-20260007619-A1 Sublingual Epinephrine Compositions Including pH-Modifying Excipients And Penetration Enhancers And Methods for Use Thereof CMA1, ADRB3, ENPP2 HSP90AA1 4163/4885GLA 2688/4885HRH1 35/4885
US-20110206764-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS SLC35A1, SLC29A2, NEU2 HSP90AA1 3591/4885GLA 314/4885HRH1 1062/4885
US-20140072627-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS SLC35A1, SLC29A2, NEU2 HSP90AA1 3591/4885GLA 314/4885HRH1 1062/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.