Azelaic Acid

Azelaic Acid

SCHEMBL4157618

Cl.O=C(O)CCCCCCCC(=O)O

nearest known ligand 0.92

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 Azelaic 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 6/20 0.67
HDAC11 known ✓ Q96DB2 5/20 0.67
ESR1 known ✓ P03372 1/20 0.67
PDE4A known ✓ P27815 1/20 0.67
PDE3A known ✓ Q14432 1/20 0.67
SLC6A2 known ✓ P23975 1/20 0.67
SLC6A3 known ✓ Q01959 1/20 0.67
TSHR P16473 5/20 0.92
LMNA P02545 3/20 0.92
NFKB1 P19838 1/20 0.92
PMP22 Q01453 1/20 0.92
SLC22A6 Q4U2R8 2/20 0.71
GPR84 Q9NQS5 8/20 0.71
FFAR1 O14842 2/20 0.71
FFAR4 Q5NUL3 2/20 0.71
PPARD Q03181 6/20 0.67
PPARA Q07869 6/20 0.67
ALDH1A1 P00352 3/20 0.67
TLR2 O60603 2/20 0.67
TDP1 Q9NUW8 2/20 0.67

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 SCHEMBL688374 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL7717227 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Hydrochloric Acid SCHEMBL8921154 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL14809040 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Hydrochloric Acid SCHEMBL19210205 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL14809563 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Hydrochloric Acid SCHEMBL8922192 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Hydrochloric Acid SCHEMBL7717229 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL689154 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6
Hydrochloric Acid SCHEMBL8923793 1.00 TSHR (0.92) TSHRLMNANFKB1PMP22SLC22A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023231317-A1 NANOFILTRATION MEMBRANE PREPARATION METHOD AND NANOFILTRATION MEMBRANE PREPARED THEREBY 沃顿科技股份有限公司 2023-12-07 WO claimed
CN-109161024-B Alkali-resistant modified polyether block amino silicone oil and preparation method thereof 清远市宏图助剂有限公司 2021-06-15 CN claimed
CN-111961426-A Joint filling sealing material, preparation method and application thereof 嘉兴市爵拓科技有限公司 2020-11-20 CN claimed
CN-105693612-B Bridging type arylpyrazole type amide compound and its solvent heat one-pot synthesis method and application 中南民族大学 2019-01-08 CN claimed
EP-0161549-B1 ACID HALIDE FUNCTIONAL MATERIALS DSM RIM NYLON V.O.F (NL) 1988-11-17 EP claimed
EP-0067695-B1 PROCESS FOR THE PREPARATON OF NYLON BLOCK POLYMERS DSM RIM NYLON V.O.F (NL) 1986-10-15 EP claimed
EP-0067693-B1 ACID HALIDE AND ACYLLACTAM FUNCTIONAL MATERIALS DSM RIM NYLON V.O.F (NL) 1986-09-10 EP claimed
US-4590243-A USING ACYLLACTAM FUNCTIONAL MATERIALS MONSANTO COMPANY (US) 1986-05-20 US claimed
US-4590244-A CHEMICAL INTERMEDIATES FOR NYLON BLOCK POLYMERS MONSANTO COMPANY (US) 1986-05-20 US claimed
US-4581419-A POLYMERS HAVING HYDROXY END GROUPS MODIFIED BY A DICARBOXYLIC ACIDAND A LACTAM; NYLON MOLDING MATERIALS MONSANTO COMPANY (US) 1986-04-08 US claimed
EP-0161549-A1 Acid halide functional materials DSM RIM NYLON V.O.F (NL) 1985-11-21 EP claimed
EP-0067695-A1 Process for the preparaton of nylon block polymers DSM RIM NYLON V.O.F (NL) 1982-12-22 EP claimed
EP-0067693-A1 Acid halide and acyllactam functional materials DSM RIM NYLON V.O.F (NL) 1982-12-22 EP claimed
JP-63198674-A None JP disclosed
US-20260117059-A1 CURABLE RESIN, CURABLE RESIN COMPOSITION, CURED PRODUCT, PREPREG, LAMINATE, AND SEMICONDUCTOR SUBSTRATE NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2026-04-30 US disclosed
US-20260109854-A1 CURABLE RESIN COMPOSITION, AND CURED PRODUCT THEREOF NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2026-04-23 US disclosed
EP-0148149-A2 High concentration encapsulation by interfacial polycondensation Monsanto Company (US) 1985-07-10 EP disclosed
EP-0067695-A1 Process for the preparaton of nylon block polymers DSM RIM NYLON V.O.F (NL) 1982-12-22 EP disclosed
EP-0067694-A1 Acid halide and acyllactam functional materials and process for the preparation of nylon block polymers therewith DSM RIM NYLON V.O.F (NL) 1982-12-22 EP disclosed
EP-0067693-A1 Acid halide and acyllactam functional materials DSM RIM NYLON V.O.F (NL) 1982-12-22 EP disclosed

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

For each of this compound's patents that has machine-readable text (2 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-20260109854-A1 CURABLE RESIN COMPOSITION, AND CURED PRODUCT THEREOF MLLT1, CRBN, POT1 PPARG 3473/4885HDAC11 670/4885ESR1 385/4885
US-20260117059-A1 CURABLE RESIN, CURABLE RESIN COMPOSITION, CURED PRODUCT, PREPREG, LAMINATE, AND SEMICONDUCTOR SUBSTRATE RAD51, ASH2L, H1-0 PPARG 3637/4885HDAC11 1482/4885ESR1 227/4885

“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.