Benzoin

Benzoin

SCHEMBL337105

CC(=O)O.O=C(c1ccccc1)C(O)c1ccccc1

nearest known ligand 0.88

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of Benzoin. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.88
CES2 O00748 5/20 0.88
CES1 P23141 4/20 0.88
ALDH1A1 P00352 3/20 0.66
KDM4E B2RXH2 1/20 0.66
TDP1 Q9NUW8 1/20 0.57
L3MBTL1 Q9Y468 1/20 0.57
MAPK1 P28482 1/20 0.56
HPGD P15428 1/20 0.55
CYP3A4 P08684 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.45
NPSR1 Q6W5P4 1/20 0.45
HSD17B10 Q99714 1/20 0.43

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
Benzoin SCHEMBL8865268 0.96 LMNA (0.88) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL28144567 0.94 LMNA (0.78) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL9490022 0.94 LMNA (0.84) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL4557692 0.94 LMNA (0.91) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL10665271 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL145 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL5833429 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL2025536 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL901258 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E
Benzoin SCHEMBL27696284 0.94 CES2 (1.00) LMNACES2CES1ALDH1A1KDM4E

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 1170 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115417954-B Photo-thermal dual-curing polyurethane polymer, preparation method and composite material thereof 万华化学(北京)有限公司 2025-04-01 CN claimed
CN-119505116-A Composition of photopolymerisable controlled distribution block polymer, preparation method and application thereof 中国石油化工股份有限公司 2025-02-25 CN claimed
US-20240384064-A1 3D PRINTING RESIN WITH SEPARATION EFFECT Pro3dure Medical GmbH (DE) 2024-11-21 US claimed
US-12134670-B2 Composition used in 3D printing system, its application thereof BASF SE (DE) 2024-11-05 US claimed
EP-4404866-A1 3D PRINTING RESIN WITH SEPARATION EFFECT PRO3DURE MEDICAL GMBH (DE) 2024-07-31 EP claimed
US-20240141091-A1 Block Copolymer Composition And Methods Of Preparation Thereof Kraton Corporation (US) 2024-05-02 US claimed
CN-115177793-B Method for modifying mussel protein-polyglutamic acid antibacterial lubrication medical hydrogel coating on surface of substrate 南京工业大学 2024-01-19 CN claimed
WO-2023046869-A1 3D PRINTING RESIN WITH SEPARATION EFFECT Pro3dure Medical GmbH (DE) 2023-03-30 WO claimed
EP-4154842-A1 3D PRINTING RESIN WITH SEPARATION EFFECT PRO3DURE MEDICAL GMBH (DE) 2023-03-29 EP claimed
CN-115417954-A Photo-thermal dual-curable polyurethane polymer, preparation method and composite material thereof 万华化学(北京)有限公司 2022-12-02 CN claimed
US-7012118-B2 Photopolymerizable compositions and flexographic plates prepared from controlled distribution block copolymers KRATON POLYMERS U.S. LLC (US) 2006-03-14 US claimed
US-20040072951-A1 Photopolymerizable compositions and flexographic plates prepared from controlled distribution block copolymers KRATON CHEMICAL, LLC 2004-04-15 US claimed
US-6664024-B1 Photopolymerizable epoxide compound, photoinitiator, photoactivated color changer, and reactive polysilsesquioxane compound; colorimetric analysis; stereolithography AMERICAN DYE SOURCE, INC. (CA) 2003-12-16 US claimed
US-6596787-B1 Low intensity UV curable adhesives formulated using a blend of acrylate oligomers and monomers which are capable of bonding glass, provide improved low-yellowing properties and fast cure speed over current glass bonding adhesives, bonding strength HENKEL LOCTITE CORPORATION 2003-07-22 US claimed
US-6245711-B1 Thermal paper with security features NCR CORPORATION 2001-06-12 US claimed
EP-0043480-B1 PROCESS FOR FORMING METALLIC IMAGES Hitachi, Ltd. (JP) 1985-04-03 EP claimed
US-4347304-A PHOTOSENSITIZATION WITH DISILANES OR ORGANIC COMPOUNDS HAVING COUPLED GERMANIUM OR TIN MOLECULES; PHOTORESISTS; POSITIVES; PLATING HITACHI, LTD. (JP) 1982-08-31 US claimed
EP-0043480-A2 Process for forming metallic images Hitachi, Ltd. (JP) 1982-01-13 EP claimed
US-4048036-A CURING, PHOTOINITIATOR PPG INDUSTRIES, INC. (US) 1977-09-13 US claimed
US-3980483-A Photocurable composition NIPPON OIL SEAL INDUSTRY CO., LTD. (JA) 1976-09-14 US claimed