4-Vinylphenol

4-Vinylphenol

SCHEMBL4384304

C=Cc1ccc(O)cc1.CC(=O)O

nearest known ligand 0.52

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Known targets — ChEMBL curated mechanism

ADRA2AADRA2BADRA2CADRB2AGTR1AVPR1AAVPR1BAVPR2BDKRB2CALCRCHRNA3CHRNB4ESR1ESR2GHSRGNRHRGSC1HSPA8MALT1MC1RMC4RNOS1NOS2NOS3OPRK1OXTRRAMP1RAMP2RAMP3SCN5ASSTR1SSTR2SSTR3SSTR4SSTR5dacAdacBdacCfolPftsImrcAmrcBmrdArplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of 4-Vinylphenol. 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
ESR1 known ✓ P03372 2/20 0.48
ESR2 known ✓ Q92731 2/20 0.48
ALDH1A1 P00352 4/20 0.52
KDM4E B2RXH2 2/20 0.52
TYR P14679 4/20 0.48
CA12 O43570 3/20 0.48
CA1 P00915 3/20 0.48
CA2 P00918 3/20 0.48
CA7 P43166 3/20 0.48
CA9 Q16790 3/20 0.48
CA14 Q9ULX7 3/20 0.48
AKR1B10 O60218 2/20 0.48
AKR1B1 P15121 2/20 0.48
PKM P14618 2/20 0.48
CA3 P07451 2/20 0.48
CA4 P22748 2/20 0.48
CA6 P23280 2/20 0.48
CA5A P35218 2/20 0.48
CA5B Q9Y2D0 2/20 0.48
DPP4 P27487 1/20 0.48

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
4-Vinylphenol SCHEMBL28941792 0.91 ALDH1A1 (0.55) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL4385918 0.90 ALDH1A1 (0.47) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL28399759 0.86 TYR (0.54) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL11251558 0.86 ALDH1A1 (0.50) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL8380331 0.86 ALDH1A1 (0.44) ALDH1A1KDM4ETYRCA12CA1
4-Hydroxyacetophenone SCHEMBL8726133 0.85 HSD17B1 (0.61) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL170622 0.85 ALDH1A1 (0.69) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL59328 0.85
4-Vinylphenol SCHEMBL7740604 0.84 TYR (0.63) ALDH1A1KDM4ETYRCA12CA1
4-Vinylphenol SCHEMBL8519569 0.84 ALDH1A1 (0.48) ALDH1A1KDM4ETYRCA12CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115612126-A Cross-linked polystyrene solid acid catalyst with polymerization inhibition function and preparation method and application thereof 江苏集萃光敏电子材料研究所有限公司 2023-01-17 CN claimed
CN-115612126-B Crosslinked polystyrene solid acid catalyst with polymerization inhibition function, and preparation method and application thereof 江苏集萃光敏电子材料研究所有限公司 2024-02-20 CN disclosed
CN-115612126-A Cross-linked polystyrene solid acid catalyst with polymerization inhibition function and preparation method and application thereof 江苏集萃光敏电子材料研究所有限公司 2023-01-17 CN disclosed
CN-105669889-A Styrene derivative-methacrylate copolymer containing photo-acid generation groups as well as preparation and application of styrene derivative-methacrylate copolymer 北京师范大学 2016-06-15 CN disclosed
US-7629400-B2 Image making medium HYMAN SYDNEY 2009-12-08 US disclosed
US-20030035917-A1 Image making medium HYMAN SYDNEY (US) 2003-02-20 US disclosed
US-5330627-A Thermosetting coating compositions and their use HERBERTS G.M.B.H. (DE) 1994-07-19 US disclosed