Palmitoyl-Carnitine

Palmitoyl-Carnitine

SCHEMBL515545

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

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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
▸ MAPK1 P28482 5/20 1.00
▸ MAPT P10636 5/20 1.00
▸ LMNA P02545 4/20 1.00
▸ GMNN O75496 3/20 1.00
▸ NPSR1 Q6W5P4 3/20 1.00
▸ MEN1 O00255 3/20 1.00
▸ KMT2A Q03164 3/20 1.00
▸ HSP90AA1 P07900 2/20 1.00
▸ BLM P54132 2/20 1.00
▸ NR1H4 Q96RI1 2/20 1.00
▸ GLA P06280 1/20 1.00
▸ PMP22 Q01453 1/20 1.00
▸ CYP1A2 P05177 3/20 0.97
▸ TP53 P04637 3/20 0.97
▸ TSHR P16473 3/20 0.97
▸ CYP2C9 P11712 2/20 0.97
▸ HIF1A Q16665 2/20 0.97
▸ SLC25A20 O43772 3/20 0.74
▸ CYP2D6 P10635 2/20 0.74
▸ SLC6A5 Q9Y345 2/20 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 SCHEMBL17667555 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL8620445 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL8580303 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL1321243 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL8580295 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Octanoylcarnitine SCHEMBL16535179 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Palmitoyl-Carnitine SCHEMBL2785480 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL8620442 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Hydrochloric Acid SCHEMBL8620437 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1
Palmitoyl-Carnitine SCHEMBL20580076 1.00 MAPK1 (1.00) MAPK1MAPTLMNAGMNNNPSR1

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 490 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
CN-118105365-A Use of a compound in the manufacture of a medicament for preventing or treating idiopathic vomiting in a companion animal 马斯公司 2024-05-31 — — CN claimed
US-20230390225-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE FLORIDA STATE UNIVERSITY RESEARCH FOUNDATION, INC. 2023-12-07 — — US 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-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
US-20020137692-A1 Novel compositions of potassium channel openers and protein kinase C inhibitors and use thereof PHARMACIA AB 2002-09-26 — — US 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 (6 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 MAPK1 3318/4885MAPT 1557/4885LMNA 3485/4885
US-20240261411-A1 PERMEATION ENHANCERS FOR GASTROINTESTINAL SYNTHETIC EPITHELIAL LININGS FABP2, SLC10A2, FABP6 MAPK1 3260/4885MAPT 4404/4885LMNA 4353/4885
US-20230390225-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE TMPRSS2, NCSTN, PRSS2 MAPK1 3318/4885MAPT 1557/4885LMNA 3485/4885
US-20260007622-A1 NICLOSAMIDE FORMULATIONS AND METHODS OF USE TMPRSS2, PKD2, DSP MAPK1 2391/4885MAPT 1835/4885LMNA 1816/4885
US-20260007619-A1 Sublingual Epinephrine Compositions Including pH-Modifying Excipients And Penetration Enhancers And Methods for Use Thereof CMA1, ADRB3, ENPP2 MAPK1 2807/4885MAPT 2116/4885LMNA 1000/4885
US-20110206764-A1 FORMULATIONS FOR ENHANCED BIOAVAILABILITY OF ORALLY ADMINISTERED POLAR AGENTS SLC35A1, SLC29A2, NEU2 MAPK1 1997/4885MAPT 3202/4885LMNA 774/4885

“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.

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