Pimelic Acid

Pimelic Acid

SCHEMBL2304128

O=C(O)CCCCC(=O)O.O=C(O)CCCCCC(=O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2SLC6A2SLC6A3

The experimentally established mechanism targets of Pimelic 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
▸ SLC6A2 known ✓ P23975 1/20 0.71
▸ SLC6A3 known ✓ Q01959 1/20 0.71
▸ TSHR P16473 5/20 1.00
▸ LMNA P02545 3/20 1.00
▸ NFKB1 P19838 1/20 1.00
▸ PMP22 Q01453 1/20 1.00
▸ SLC22A6 Q4U2R8 2/20 0.77
▸ GPR84 Q9NQS5 8/20 0.75
▸ FFAR1 O14842 2/20 0.75
▸ FFAR4 Q5NUL3 2/20 0.75
▸ PPARG P37231 7/20 0.71
▸ PPARD Q03181 7/20 0.71
▸ PPARA Q07869 7/20 0.71
▸ HDAC11 Q96DB2 5/20 0.71
▸ ALDH1A1 P00352 3/20 0.71
▸ PTPN1 P18031 3/20 0.71
▸ TLR2 O60603 2/20 0.71
▸ TDP1 Q9NUW8 2/20 0.71
▸ MEN1 O00255 2/20 0.71
▸ FABP4 P15090 2/20 0.71

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
SCHEMBL1197865 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
Azelaic Acid SCHEMBL7203725 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
SCHEMBL3814949 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
Azelaic Acid SCHEMBL6462921 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
SCHEMBL3493631 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
SCHEMBL1235383 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
SCHEMBL25186232 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
Octanedioate SCHEMBL5799504 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
SCHEMBL21065467 1.00 TSHR (1.00) TSHRLMNANFKB1PMP22SLC22A6
Sebacic Acid SCHEMBL20500595 1.00 TSHR (1.00) 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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115073889-A High polymer material with good water retention and preparation method thereof 江苏睿安应用生物技术股份有限公司 2022-09-20 — — CN disclosed
US-20210246273-A1 Cellulose Nanofiber-Containing Aqueous Dispersion ASAHI KASEI KABUSHIKI KAISHA (JP) 2021-08-12 — — US disclosed
EP-3010956-B1 HYPERBRANCHED POLYMERS DSM IP ASSETS BV (NL) 2020-04-29 — — EP disclosed
US-20200071733-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE LYGOS, INC. 2020-03-05 — — US disclosed
EP-3404094-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE Lygos, Inc. (US) 2018-11-21 — — EP disclosed
EP-2823032-B1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE LYGOS INC (US) 2018-08-22 — — EP disclosed
EP-3010956-A1 HYPERBRANCHED POLYMERS DSM IP Assets B.V. (NL) 2016-04-27 — — EP disclosed
EP-2794729-B1 HYPERBRANCHED POLYMERS DSM IP ASSETS BV (NL) 2016-04-13 — — EP disclosed
EP-2823032-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE Lygos, Inc. (US) 2015-01-14 — — EP disclosed
EP-2822944-A1 OXAZOLIDINONE COMPOUNDS AND DERIVATIVES THEREOF AMGEN, INC. (US) 2015-01-14 — — EP disclosed
CN-101528993-A Spandex fibers containing partially dehydroxylated hydrotalcite HYOSUNG CORP (KR) 2009-09-09 — — CN disclosed
US-6927237-B2 Two solvent antimicrobial compositions and methods employing them ECOLAB INC. (US) 2005-08-09 — — US disclosed
US-20050096245-A1 Two solvent antimicrobial compositions and methods employing them ECOLAB INC. (US) 2005-05-05 — — US disclosed
US-20020168422-A1 Two solvent antimicrobial compositions and methods employing them ECOLAB USA INC. 2002-11-14 — — US disclosed
EP-1192178-A2 RUFOMYCINS AND DERIVATIVES THEREOF USEFUL AS INHIBITORS OF MULTI-DRUG RESISTANCE ASSOCIATED PROTEIN-1 (MRP-1) ELI LILLY AND COMPANY (US) 2002-04-03 — — EP disclosed
WO-2000078795-A2 RUFOMYCINS AND DERIVATIVES THEREOF USEFUL AS INHIBITORS OF MULTI-DRUG RESISTANCE ASSOCIATED PROTEIN-1 (MRP-1) ELI LILLY AND COMPANY (US) 2000-12-28 — — WO disclosed
WO-2000078797-A1 RUFOMYCIN DERIVATIVES USEFUL AS ANTIBIOTICS ELI LILLY AND COMPANY (US) 2000-12-28 — — WO disclosed
US-5260120-A Coating with primer, heating and drying, then applying protective coating yields zinc coated metal substrate which does not deteriorate welding electrode MORTON INTERNATIONAL, INC. (US) 1993-11-09 — — US disclosed
EP-0545605-A2 Two coat weldable primer for steel MORTON INTERNATIONAL, INC. (US) 1993-06-09 — — EP disclosed
US-4175064-A COBALT AND POTASSIUM CARBOXYLIC ACID SALTS TENNECO CHEMICALS, INC. (US) 1979-11-20 — — US 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-20200071733-A1 RECOMBINANT HOST CELLS FOR THE PRODUCTION OF MALONATE ME1, MAL2, ME3 SLC6A2 3493/4885SLC6A3 4016/4885TSHR 2970/4885
US-20020168422-A1 Two solvent antimicrobial compositions and methods employing them TAS2R50, HDHD5, CEL SLC6A2 3165/4885SLC6A3 3507/4885TSHR 4520/4885

“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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