Carnitine

Carnitine

SCHEMBL9901519

C[N+](C)(C)CC(O)CC(=O)[O-].NCCCCC(N)C(=O)O

nearest known ligand 0.59

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPARDPTGS1PTGS2dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Carnitine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
▸ GSR P00390 1/20 0.59
▸ SLC22A16 Q86VW1 1/20 0.59
▸ CPT2 P23786 1/20 0.47
▸ CPT1A P50416 1/20 0.47
▸ MAPT P10636 1/20 0.42
▸ ARG2 P78540 4/20 0.39
▸ ARG1 P05089 3/20 0.39
▸ NOS2 P35228 5/20 0.39
▸ NOS1 P29475 4/20 0.39
▸ NOS3 P29474 3/20 0.39
▸ CYP1A2 P05177 2/20 0.39
▸ CYP3A4 P08684 1/20 0.39
▸ TSHR P16473 1/20 0.39
▸ BLM P54132 1/20 0.38
▸ RNPEP Q9H4A4 1/20 0.38
▸ MEN1 O00255 2/20 0.36
▸ KMT2A Q03164 2/20 0.36
▸ CYP2C19 P33261 1/20 0.36
▸ HRH1 P35367 1/20 0.36

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
Levocarnitine SCHEMBL6553881 1.00 GSR (0.59) GSRSLC22A16CPT2CPT1AMAPT
Carnitine SCHEMBL9128766 1.00 GSR (0.59) GSRSLC22A16CPT2CPT1AMAPT
Carnitine SCHEMBL27486119 0.94 SLC22A16 (0.59) GSRSLC22A16CPT2CPT1AMAPT
Carnitine SCHEMBL28276640 0.88 SLC22A16 (0.51) GSRSLC22A16CPT2CPT1AMAPT
Levocarnitine SCHEMBL2447788 0.86 GSR (0.56) GSRSLC22A16MAPTARG2ARG1
Carnitine SCHEMBL27798506 0.84 SLC22A16 (0.61) GSRSLC22A16CPT2CPT1AMAPT
Lysine SCHEMBL4622301 0.83 GSR (0.65) GSRCPT2CPT1AARG2ARG1
Lysine SCHEMBL273053 0.83 GSR (0.65) GSRCPT2CPT1AARG2ARG1
Levocarnitine SCHEMBL6635924 0.82 SLC22A16 (0.59) GSRSLC22A16CPT2CPT1AMAPT
Carnitine SCHEMBL27492466 0.82 SLC22A16 (0.59) GSRSLC22A16CPT2CPT1AMAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110760449-B Geotrichum galactose ZJPH1810 and application thereof in preparation of (S) -1- (2, 6-dichloro-3-fluorophenyl) ethanol 浙江工业大学 2021-04-06 — — CN claimed
CN-110760449-A Geotrichum galactose ZJPH1810 and application thereof in preparation of (S) -1- (2, 6-dichloro-3-fluorophenyl) ethanol 浙江工业大学 2020-02-07 — — CN claimed
CN-113876946-B Combined pharmaceutical application of PD-1 antibody and pseudomonas aeruginosa and pharmaceutical composition 神威药业集团有限公司 2024-03-26 — — CN disclosed
WO-2023050694-A1 COMBINED PHARMACEUTICAL USE OF PD-1 ANTIBODY AND PSEUDOMONAS AERUGINOSA AND PHARMACEUTICAL COMPOSITION THEREOF 神威药业集团有限公司 2023-04-06 — — WO disclosed
CN-113876946-A Combined pharmaceutical application and pharmaceutical composition of PD-1 antibody and pseudomonas aeruginosa 神威药业集团有限公司 2022-01-04 — — CN disclosed
CN-112048538-B Method for preparing (S) - [3, 5-bis (trifluoromethyl) phenyl ] ethanol by using Verticillium terrestris 浙江工业大学 2021-12-21 — — CN disclosed
CN-110760449-B Geotrichum galactose ZJPH1810 and application thereof in preparation of (S) -1- (2, 6-dichloro-3-fluorophenyl) ethanol 浙江工业大学 2021-04-06 — — CN disclosed
CN-112048538-A Method for preparing (S) - [3, 5-bis (trifluoromethyl) phenyl ] ethanol by using Verticillium terrestris 浙江工业大学 2020-12-08 — — CN disclosed
CN-110760449-A Geotrichum galactose ZJPH1810 and application thereof in preparation of (S) -1- (2, 6-dichloro-3-fluorophenyl) ethanol 浙江工业大学 2020-02-07 — — CN disclosed
CN-103347521-B Chemotherapy and the method for the metabolism target cancer cell of immunization therapy are used for treating cancer 全球癌症治疗有限责任公司 2018-05-25 — — CN disclosed
US-20180117249-A1 Warburg Effect Targeted Chemotherapy Apparatus CURE CANCER WORLDWIDE LLC (US) 2018-05-03 — — US disclosed
EP-2959291-A1 METHODS OF DIAGNOSING AND TREATING CANCER BY DETECTING AND MANIPULATING MICROBES IN TUMORS John Wayne Cancer Institute (US) 2015-12-30 — — EP disclosed
US-20140271557-A1 METHODS OF DIAGNOSING AND TREATING CANCER BY DETECTING AND MANIPULATING MICROBES IN TUMORS LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBOR-UCLA MEDICAL CENTER 2014-09-18 — — US disclosed
WO-2014130162-A1 METHODS OF DIAGNOSING AND TREATING CANCER BY DETECTING AND MANIPULATING MICROBES IN TUMORS LEE DELPHINE J (US) 2014-08-28 — — WO disclosed
US-20140056844-A1 METHODS OF METABOLIC TARGETING CANCER CELLS USING CHEMO- AND IMMUNOTHERAPY FOR TREATING CANCER CURE CANCER WORLDWIDE LLC 2014-02-27 — — US disclosed
EP-2648734-A1 METHODS OF METABOLIC TARGETING CANCER CELLS USING CHE MO- AND IMMUNOTHERAPY FOR TREATING CANCER Cure Cancer Worldwide Corporation (US) 2013-10-16 — — EP disclosed
CN-103347521-A Methods of metabolic targeting cancer cells using che mo- and immunotherapy for treating cancer CURE CANCER WORLDWIDE CORP 2013-10-09 — — CN disclosed
WO-2012075679-A1 METHODS OF METABOLIC TARGETING CANCER CELLS USING CHE MO- AND IMMUNOTHERAPY FOR TREATING CANCER CURE CANCER WORLDWIDE CORPORATION (US) 2012-06-14 — — WO disclosed
CN-1196672-C Non-hydroscopic salts of active ingredients having therapeutical and/or nutritional activities and orally administrable compositions containing same BIOSALTS SRL (IT) 2005-04-13 — — CN disclosed
CN-1162397-C Therapeutically and/or nutritionaly enhanced derivatives of active ingredients and orally administrable compsns. contg. same �����ι�˾ 2004-08-18 — — CN disclosed
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