Adipic Acid

Adipic Acid

SCHEMBL6543544

CC1(C)CCCC(C)(C)N1.CC1(C)CCCC(C)(C)N1.O=C(O)CCCCC(=O)O

nearest known ligand 0.46

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC18A2SLC6A2SLC6A3

The experimentally established mechanism targets of Adipic 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
LMNA P02545 2/20 0.46
TSHR P16473 5/20 0.44
NFKB1 P19838 1/20 0.44
PMP22 Q01453 1/20 0.44
AKR1B1 P15121 1/20 0.43
GPR84 Q9NQS5 8/20 0.41
PPARG P37231 7/20 0.41
PPARD Q03181 7/20 0.41
PPARA Q07869 7/20 0.41
HDAC11 Q96DB2 5/20 0.41
PTPN1 P18031 3/20 0.41
ALDH1A1 P00352 2/20 0.41
TLR2 O60603 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
FABP4 P15090 2/20 0.41
SLC22A6 Q4U2R8 2/20 0.41
SLC22A8 Q8TCC7 1/20 0.41
MEN1 O00255 1/20 0.41
ESR1 P03372 1/20 0.41
ALOX15 P16050 1/20 0.41

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
Adipic Acid SCHEMBL27539142 1.00 LMNA (0.46) LMNATSHRNFKB1PMP22AKR1B1
Sebacic Acid SCHEMBL2344968 0.98 TSHR (0.48) LMNATSHRNFKB1PMP22AKR1B1
Sebacic Acid SCHEMBL8067661 0.98 TSHR (0.48) LMNATSHRNFKB1PMP22AKR1B1
Succinic Acid SCHEMBL28499250 0.91 EGLN1 (0.41) LMNAALDH1A1SLC22A6OR51E2BBOX1
Succinic Acid SCHEMBL2342959 0.91 EGLN1 (0.41) LMNAALDH1A1SLC22A6OR51E2BBOX1
Palmitic Acid SCHEMBL28380297 0.91 GPR84 (0.59) LMNATSHRAKR1B1GPR84PPARG
Stearic Acid SCHEMBL27656171 0.91 GPR84 (0.59) LMNATSHRAKR1B1GPR84PPARG
Sebacic Acid SCHEMBL9506634 0.88 TSHR (0.39) LMNATSHRNFKB1PMP22AKR1B1
Beta-Alanine SCHEMBL27842605 0.84 LMNA (0.37) LMNATSHRNFKB1HDAC11ALDH1A1
Acetic Acid SCHEMBL986871 0.80 FFAR3 (0.38) TSHRNFKB1ALDH1A1MEN1KMT2A

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-107921221-B Assembly for syringe, prefilled syringe, seal cap for outer cylinder, and assembly package for syringe 泰尔茂株式会社 2021-07-20 CN disclosed
US-20040122270-A1 In-situ polymerization of monoethylenically unsaturated monomers with secondary amines BAYER AKTIENGESELLSCHAFT (DE) 2004-06-24 US disclosed
EP-1428838-A1 In situ-polymerization of monoethylenically unsaturated monomers with secondary amines Bayer MaterialScience AG (DE) 2004-06-16 EP disclosed
EP-1428839-A1 In-situ polymerization of monoethylenically unsaturated monomers with secondary amines Bayer MaterialScience AG (DE) 2004-06-16 EP disclosed
EP-1052112-B1 Color developer composition, aqueous dispersion, recording sheet and color developing ink MITSUI CHEMICALS INC (JP) 2004-02-04 EP disclosed
US-6686424-B2 USE IN RADICAL POLYMERIZATION; REACTING AN OXIDIZING AGENT WITH A STERICALLY HINDERED SECONDARY AMINE TO PRODUCE A NITROXY RADICAL; ADDING TO THE NITROXY RADICAL ONE OR MORE VINYL MONOMER BAYER AKTIENGESELLSCHAFT (DE) 2004-02-03 US disclosed
EP-1375457-A1 One-pot process for the preparation of functionalized alkoxyamines Bayer Aktiengesellschaft (DE) 2004-01-02 EP disclosed
EP-1375476-A1 A new process for the synthesis of alkoxyamines active in controlled radical polymerization Bayer Aktiengesellschaft (DE) 2004-01-02 EP disclosed
US-20040002606-A1 Process for the synthesis for alkoxy amines and their use in controlled radical polymerization BAYER AKTIENGESELLSCHAFT (DE) 2004-01-01 US disclosed
US-20030236368-A1 PREPARATION OF FUNCTIONALIZED ALKOXYAMINE INITIATOR AND ITS USE BAYER AKTIENGESELLSCHAFT (DE) 2003-12-25 US disclosed
US-6383982-B1 DYE DEVELOPERS FOR COLORING, METAL SALICYLATE AND POLYESTER POLYOLS WITH CARBONATE OR ESTER MITSUI CHEMICALS, INC. (JP) 2002-05-07 US disclosed
EP-1052112-A2 Color developer composition, aqueous dispersion, recording sheet and color developing ink Mitsui Chemicals, Inc. (JP) 2000-11-15 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 (3 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-20030236368-A1 PREPARATION OF FUNCTIONALIZED ALKOXYAMINE INITIATOR AND ITS USE NOS1, NOS2, CBR1 LMNA 2253/4885TSHR 3966/4885NFKB1 785/4885
US-20040002606-A1 Process for the synthesis for alkoxy amines and their use in controlled radical polymerization ALKBH3, MAOB, ALKBH1 LMNA 2174/4885TSHR 4237/4885NFKB1 1356/4885
US-20040122270-A1 In-situ polymerization of monoethylenically unsaturated monomers with secondary amines ALOX5, PARG, FASN LMNA 515/4885TSHR 4635/4885NFKB1 357/4885

“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.