Stearic Acid

Stearic Acid

SCHEMBL557594

CCCCCCCCCCCCCCCCCC(=O)O.CCN(CC)CC

nearest known ligand 0.77

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

rplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Stearic 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
GPR84 Q9NQS5 7/20 0.77
PPARG P37231 7/20 0.77
PPARD Q03181 7/20 0.77
PPARA Q07869 7/20 0.77
HDAC11 Q96DB2 5/20 0.77
TSHR P16473 4/20 0.77
PTPN1 P18031 3/20 0.77
FABP4 P15090 3/20 0.77
ALDH1A1 P00352 2/20 0.77
TLR2 O60603 2/20 0.77
TDP1 Q9NUW8 2/20 0.77
KMT2A Q03164 2/20 0.77
ALOX15 P16050 2/20 0.77
HSD17B10 Q99714 2/20 0.77
SLC22A6 Q4U2R8 1/20 0.77
SLC22A8 Q8TCC7 1/20 0.77
MEN1 O00255 1/20 0.77
ESR1 P03372 1/20 0.77
PDE4A P27815 1/20 0.77
PDE3A Q14432 1/20 0.77

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
Octanoic Acid SCHEMBL3414554 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Decanoic Acid SCHEMBL5875269 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Octanoic Acid SCHEMBL3412884 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Heptanoate SCHEMBL3410001 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Undecanoate SCHEMBL21145218 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Dodecanoate SCHEMBL8469515 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Nonanoate SCHEMBL5874090 1.00 GPR84 (0.77) GPR84PPARGPPARDPPARAHDAC11
Octanoic Acid SCHEMBL28159534 0.98 GPR84 (0.74) GPR84PPARGPPARDPPARAHDAC11
Stearic Acid SCHEMBL28986985 0.98 GPR84 (0.74) GPR84PPARGPPARDPPARAHDAC11
Hexanoate SCHEMBL3411666 0.98 AKR1B1 (0.76) 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 169 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160199027-A1 ULTRASOUND PROBE COUPLERS AND RELATED METHODS SCULLY, CASEY K. 2016-07-14 US claimed
WO-2006114140-A1 PRISTANIC ACID-CONTAINING COSMETIC PREPARATIONS BEIERSDORF AG (DE) 2006-11-02 WO claimed
US-5863524-A INCLUDING A POLYAMINE CLARIFIER WITH AN ALKALI METAL BICARBONATE OR CARBONATE, A POLYHYDRIC ALCOHOL, A FATTY ACID SALT AND WATER; STABILITY; FEEL CHURCH & DWIGHT CO., INC. (US) 1999-01-26 US claimed
EP-3538225-B1 ALUMINUM-FREE ANTIPERSPIRANT/DEODORANT COMPOSITIONS COLGATE PALMOLIVE CO (US) 2026-04-01 EP disclosed
US-20240325266-A1 Personal Care Compositions COLGATE-PALMOLIVE COMPANY (US) 2024-10-03 US disclosed
US-20230340317-A1 METHOD AND APPLICATIONS OF NONSTOICHIOMETRIC IONIC EMULSIONS SAUDI ARABIAN OIL COMPANY (SA) 2023-10-26 US disclosed
EP-2948505-B1 THERMOPLASTIC COMPOSITIONS CONTAINING NANOSCALE-SIZED PARTICLE ADDITIVES FOR LASER DIRECT STRUCTURING AND METHODS FOR THE MANUFACTURE AND USE THEREOF SHPP GLOBAL TECH BV (NL) 2022-11-16 EP disclosed
US-11147755-B2 Aluminum-free antiperspirant / deodorant compositions COLGATE-PALMOLIVE COMPANY (US) 2021-10-19 US disclosed
CN-107158050-B Hydrangea paniculata total coumarin glycoside, preparation method, composition and application thereof 中国医学科学院药物研究所 2021-08-13 CN disclosed
CN-104447900-B Preparation activity, application and quality control of new compound 石任兵 2021-08-06 CN disclosed
CN-103989966-B Medicine composition for preventing and treating migraine disease and preparation method and application thereof 石任兵 2021-05-25 CN disclosed
US-5241003-A Post-treated polyisobutenyl succinimide; crankcase, transmission oils ETHYL PETROLEUM ADDITIVES, INC. (US) 1993-08-31 US disclosed
EP-0531585-A1 Oil additive concentrates and lubricants of enhanced performance capabilities ETHYL PETROLEUM ADDITIVES LIMITED (GB) 1993-03-17 EP disclosed
EP-0531000-A1 Oil additive concentrates and lubricants of enhanced performance capabilities ETHYL PETROLEUM ADDITIVES, INC. (US) 1993-03-10 EP disclosed
US-5137980-A Reacting polyisobutene with aacidic reactant; super atmospheric pressure; low tar rating ETHYL PETROLEUM ADDITIVES, INC. (US) 1992-08-11 US disclosed
EP-0459656-A1 Lubricant compositions ETHYL PETROLEUM ADDITIVES, INC. (US) 1991-12-04 EP disclosed
US-5066743-A Bonding nonpolar surfaces such as polyethylene and polypropylene LOCTITE CORPORATION (US) 1991-11-19 US disclosed
EP-0430624-A1 Gear oils and additives therefor ETHYL PETROLEUM ADDITIVES, INC. (US) 1991-06-05 EP disclosed
EP-0428393-A1 Gear oils and additives therefor ETHYL PETROLEUM ADDITIVES, INC. (US) 1991-05-22 EP disclosed
US-4979993-A Trialkylammonium alkyl carboxylate primer for cyanoacrylate bonding of polymeric substrates LOCTITE CORPORATION (US) 1990-12-25 US disclosed