Palmitic Acid

Palmitic Acid

SCHEMBL539137

CCCCCCCCCCCCCCCC(=O)O.Cl

nearest known ligand 0.94

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 Palmitic Acid. 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
PPARG known ✓ P37231 7/20 0.94
HDAC11 known ✓ Q96DB2 5/20 0.94
ESR1 known ✓ P03372 1/20 0.94
PDE4A known ✓ P27815 1/20 0.94
PDE3A known ✓ Q14432 1/20 0.94
GPR84 Q9NQS5 7/20 0.94
PPARD Q03181 7/20 0.94
PPARA Q07869 7/20 0.94
TSHR P16473 4/20 0.94
PTPN1 P18031 3/20 0.94
FABP4 P15090 3/20 0.94
ALDH1A1 P00352 2/20 0.94
TLR2 O60603 2/20 0.94
TDP1 Q9NUW8 2/20 0.94
KMT2A Q03164 2/20 0.94
ALOX15 P16050 2/20 0.94
HSD17B10 Q99714 2/20 0.94
SLC22A6 Q4U2R8 1/20 0.94
SLC22A8 Q8TCC7 1/20 0.94
MEN1 O00255 1/20 0.94

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
Palmitic Acid SCHEMBL7556500 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Lignoceric Acid SCHEMBL3674713 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Nonanoate SCHEMBL4152676 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Pentadecanoic Acid SCHEMBL6712161 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Heptanoate SCHEMBL19994751 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Nonanoate SCHEMBL20572899 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Dodecanoate SCHEMBL23581128 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Tridecanoate SCHEMBL1994545 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Heneicosanoic Acid SCHEMBL7907716 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11
Behenic Acid SCHEMBL926255 1.00 GPR84 (0.94) GPR84PPARGPPARDPPARAHDAC11

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122012182-A Method for synthesizing branched fatty acid ester of hydroxy fatty acid by taking natural oil containing hydroxy fatty acid as raw material 江南大学 2026-05-12 CN claimed
US-20260022520-A1 METHOD FOR ACYLATING A HYDROXYLATED SOLID MATERIAL CELLULOTECH INC (CA) 2026-01-22 US claimed
CN-119139157-B Hair loss preventing and caring component, preparation method thereof and shampoo 广州市圣莎拉化妆品有限公司 2025-03-07 CN claimed
CN-119462735-A Lysophosphatidyl Process for the preparation of choline 苏州昊帆生物股份有限公司 2025-02-18 CN claimed
CN-119139157-A Hair loss preventing and caring component, preparation method thereof and shampoo 广州市圣莎拉化妆品有限公司 2024-12-17 CN claimed
CN-116554711-B Organic modified mica and preparation method and application thereof 广东省科学院生物与医学工程研究所 2024-06-07 CN claimed
WO-2024064894-A1 BIOPOLYMER AND MATERIAL COMPOSITE CONTAINMENTS DOUBLE DOUBLE D, LLC (US) 2024-03-28 WO claimed
CN-115353679-B High-strength polyethylene wax-montmorillonite modified polyethylene material and preparation method thereof 扬州科博新材料有限公司 2023-09-29 CN claimed
CN-116554711-A Organic modified mica and preparation method and application thereof 广东省科学院生物与医学工程研究所 2023-08-08 CN claimed
CN-112812005-A Preparation method of clindamycin palmitate hydrochloride intermediate palmitoyl chloride 海南海神同洲制药有限公司 2021-05-18 CN claimed
CN-103819528-B The preparation method of tea saponin cetylate tensio-active agent and product ZHEJIANG UNIVERSITY (CN) 2016-04-20 CN claimed
CN-103819528-A Preparation method of tea saponin palmitate surfactant and product UNIV ZHEJIANG 2014-05-28 CN claimed
US-20130236647-A1 MACHINE AND TREATMENT PROCESS VIA CHROMATOGENOUS GRAFTING OF A HYDROXYLATED SUBSTRATE CENTERE TECHNIQUE DU PAPIER (FR) 2013-09-12 US claimed
CN-103082036-A Oil-soluble bamboo leaf flavonoid derivative and application thereof UNIV ZHEJIANG TECHNOLOGY 2013-05-08 CN claimed
US-20100087113-A1 STEAM PERMISSIVE AND WATER NON PERMISSIVE SCREEN, AND METHOD FOR MAKING SAME SOPREMA (FR) 2010-04-08 US claimed
US-20100015425-A1 METHOD FOR MAKING A REINFORCEMENT FRAME AND SEALING MEMBRANE INCLUDING SUCH FRAME, AND PRODUCTS THUS OBTAINED SOPREMA (FR) 2010-01-21 US claimed
CN-1332967-C Clindamycin palmitate hydrochloric acid preparation method NANYANG LUCHENG BIOCHEMISTRY I (CN) 2007-08-22 CN claimed
CN-1733787-A Clindamycin palmitate hydrochloric acid preparation method NANYANG LUCHENG BIOCHEMISTRY I (CN) 2006-02-15 CN claimed
CN-1263083-A Preparation method of tea-polyphenol high-grade aliphatic ester WUXI UNIV OF LIGHT INDUSTRY (CN) 2000-08-16 CN claimed
US-4272502-A Process for preparing gaseous hydrogen chloride from dilute aqueous hydrochloric acid CHEMISCHE WERKE HULS AKTIENGESELLSCHAFT (DE) 1981-06-09 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 (1 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-20260022520-A1 METHOD FOR ACYLATING A HYDROXYLATED SOLID MATERIAL ELOVL3, ELOVL1, ACSL1 PPARG 448/4885HDAC11 728/4885ESR1 1296/4885

“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.