Butylated Hydroxytoluene

Butylated Hydroxytoluene

SCHEMBL61353

CNC.Cc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1

nearest known ligand 0.86

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.86
CA2 P00918 4/20 0.86
ALDH1A1 P00352 3/20 0.86
POLB P06746 1/20 0.86
TYR P14679 1/20 0.86
HSPA5 P11021 1/20 0.67
CYP2C9 P11712 4/20 0.64
CYP2C19 P33261 4/20 0.64
HIF1A Q16665 3/20 0.64
CA1 P00915 2/20 0.58
CYP2D6 P10635 1/20 0.56
HSD17B10 Q99714 1/20 0.56
GAA P10253 3/20 0.53
PTGS1 P23219 2/20 0.50
PTGS2 P35354 2/20 0.50
CYP1A2 P05177 1/20 0.50
HPN P05981 1/20 0.50
MAPT P10636 1/20 0.50
ALOX15 P16050 1/20 0.50
SIRT5 Q9NXA8 1/20 0.50

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
Butylated Hydroxytoluene SCHEMBL453824 0.93 SMN1; SMN2 (1.00) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL3950 0.93 SMN1; SMN2 (1.00) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL9280148 0.92 SMN1; SMN2 (0.72) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL11857289 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL20660368 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL9343307 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL7075597 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL4170581 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL11859223 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR
Butylated Hydroxytoluene SCHEMBL864242 0.90 SMN1; SMN2 (0.95) SMN1; SMN2CA2ALDH1A1POLBTYR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240376393-A1 COMPOSITION FOR CORROSION INHIBITION IN A FUEL MIXTURE AND ITS METHOD OF PREPARATION THEREOF HINDUSTAN PETROLEUM CORP LTD (IN) 2024-11-14 US claimed
EP-4461788-A1 COMPOSITION FOR CORROSION INHIBITION IN A FUEL MIXTURE AND ITS METHOD OF PREPARATION THEREOF Hindustan Petroleum Corporation Limited (IN) 2024-11-13 EP claimed
EP-3775017-B1 SPECIFIC COMPOUNDS AS ACCELERATORS FOR IMINE/METAL SALT-INITIATED RADICAL POLYMERIZATION OF UNSATURATED COMPOUNDS AND THE USE THEREOF AS ACCELERATORS FISCHERWERKE GMBH & CO KG (DE) 2024-11-06 EP claimed
US-20240294732-A1 COMPOSITIONS AND METHODS FOR PROTECTING ORGANIC POLYMERIC MATERIALS FROM DISCOLORATION DUE TO EXPOSURE TO UV-C LIGHT CYTEC INDUSTRIES INC. (US) 2024-09-05 US claimed
EP-4251689-A1 COMPOSITIONS AND METHODS FOR PROTECTING ORGANIC POLYMERIC MATERIALS FROM DISCOLORATION DUE TO EXPOSURE TO UV-C LIGHT Cytec Industries, Inc. (US) 2023-10-04 EP claimed
US-20220169828-A1 COMPOSITIONS AND METHODS FOR PROTECTING ORGANIC POLYMERIC MATERIALS FROM DISCOLORATION DUE TO EXPOSURE TO UV-C LIGHT CYTEC INDUSTRIES INC. (US) 2022-06-02 US claimed
WO-2022115573-A1 COMPOSITIONS AND METHODS FOR PROTECTING ORGANIC POLYMERIC MATERIALS FROM DISCOLORATION DUE TO EXPOSURE TO UV-C LIGHT CYTEC INDUSTRIES INC. (US) 2022-06-02 WO claimed
US-11274264-B2 Lubricating oil composition IDEMITSU KOSAN CO., LTD. (JP) 2022-03-15 US claimed
US-9321981-B2 Lubricating oil composition for internal combustion engine IDEMITSU KOSAN CO., LTD. (JP) 2016-04-26 US claimed
US-9216411-B2 Method for inhibiting nitrosamine formation in anion exchange resins DOW GLOBAL TECHNOLOGIES LLC (US) 2015-12-22 US claimed
US-20150105594-A1 STABILIZATION OF CHLOROPROPENES OCCIDENTAL CHEMICAL CORPORATION 2015-04-16 US claimed
US-7399555-B2 Separator contains a layer of polypropylene having an antioxidant with a melting point of 60 degress Celcius or higher in contact with the cathode; effective prevention of oxidative deterioration in the positive electrode, and the separator MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2008-07-15 US claimed
US-20050118510-A1 Separator contains a layer of polypropylene having an antioxidant with a melting point of 60 degress Celcius or higher in contact with the cathode; effective prevention of oxidative deterioration in the positive electrode, and the separator MATSUSHITA ELECTRIC INDUSTRIAL CO., LTD. (JP) 2005-06-02 US claimed
US-5821296-A A-SIDE COMPRISING A MULTIFUNCTIONAL ISOCYANATE AND A FREE RADICAL INITIATOR; B-SIDE COMPRISING A HYDROXYL-TERMINATED UNSATURATED POLYESTER POLYOL, AN ETHYLENICALLY UNSATURAATED MONOMER, A POLYURETHANE CATALYST, A POLYMERIZATION INHIBITOR ARISTECH CHEMICAL CORPORATION (US) 1998-10-13 US claimed
EP-0833851-A4 POLYURETHANE-POLYESTER HYBRID RESIN SYSTEM HAVING IMPROVED STABILITY ARISTECH CHEMICAL CORP (US) 1998-06-10 EP claimed
EP-0833851-A1 POLYURETHANE-POLYESTER HYBRID RESIN SYSTEM HAVING IMPROVED STABILITY Aristech Chemical Corporation (US) 1998-04-08 EP claimed
WO-1997040077-A1 POLYURETHANE-POLYESTER HYBRID RESIN SYSTEM HAVING IMPROVED STABILITY ARISTECH CHEMICAL CORPORATION (US) 1997-10-30 WO claimed
WO-2026105449-A1 CLEANING RESIN COMPOSITION AND METHOD FOR CLEANING RESIN MOLDING MACHINE 株式会社TBM 2026-05-21 WO disclosed
US-4589990-A SYNTHETIC ESTER, LOW AND HIGH MOLECULAR WEIGHT POLYISOBUTYLENE NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1986-05-20 US disclosed
US-4519932-A BLEND OF ALPHA-OLEFIN OLIGOMER, ESTER, AND POLYMETHACRYLATE NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1985-05-28 US disclosed