SCHEMBL5995848

SCHEMBL5995848

Cc1cccc(C)c1C(=O)CC[PH](=O)C(=O)c1c(C)cc(C(C)(C)C)cc1C

nearest known ligand 0.35

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ACHE P22303 3/20 0.35
RXRB P28702 4/20 0.33
RXRA P19793 3/20 0.33
TDP1 Q9NUW8 1/20 0.33
RXRG P48443 1/20 0.33
TP53 P04637 1/20 0.32
THRB P10828 1/20 0.32
SMN1; SMN2 Q16637 1/20 0.32
HTR1D P28221 1/20 0.32
HTR1B P28222 1/20 0.32
F2R P25116 1/20 0.32
NPC1 O15118 1/20 0.31
MAPT P10636 1/20 0.31
RAB9A P51151 1/20 0.31
MRGPRX4 Q96LA9 1/20 0.31
NOTUM Q6P988 1/20 0.31
CYP26A1 O43174 1/20 0.30
CYP26B1 Q9NR63 1/20 0.30
ALDH1A1 P00352 1/20 0.30

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
SCHEMBL5997838 1.00 ACHE (0.35) ACHERXRBRXRATDP1RXRG
SCHEMBL5993536 0.93 HTR1D (0.36) ACHERXRBRXRATDP1RXRG
SCHEMBL5995828 0.89 KDM4E (0.35) RXRBRXRARXRGSMN1; SMN2HTR1D
SCHEMBL5996440 0.89 KDM4E (0.35) RXRBRXRARXRGSMN1; SMN2HTR1D
SCHEMBL5995199 0.88 RAB9A (0.36) ACHERXRBRXRATDP1RXRG
SCHEMBL5994053 0.88 ACHE (0.33) ACHERXRBRXRATDP1RXRG
SCHEMBL5997924 0.87 MAPT (0.36) SMN1; SMN2F2RMAPTRAB9AALDH1A1
SCHEMBL5997542 0.87 MAPT (0.36) SMN1; SMN2F2RMAPTRAB9AALDH1A1
SCHEMBL5995486 0.86 CA12 (0.37) TDP1MAPTMRGPRX4ALDH1A1
SCHEMBL5995234 0.86 ACHE (0.35) ACHERXRBRXRATDP1RXRG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7026017-B2 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation CIBA SPECIALTY CHEMICALS CORPORATION (US) 2006-04-11 US disclosed
US-6969733-B2 Photoinitiators CIBA SPECIALTY CHEMICALS CORPORATION (US) 2005-11-29 US disclosed
US-6737549-B2 PHOTOINITIATORS FOR ACRYLATE COATINGS CIBA SPECIALTY CHEMICALS CORPORATION 2004-05-18 US disclosed
US-20030139485-A1 Photoinitiators WOLF JEAN-PIERRE (CH) 2003-07-24 US disclosed
US-20030130370-A1 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation WOLF JEAN-PIERRE (CH) 2003-07-10 US disclosed
US-20020026049-A1 Photoinitiators for acrylate coatings CIBA SPECIALTY CHEMICALS CORP. 2002-02-28 US 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-20030139485-A1 Photoinitiators DHCR24, NR1I3, CBR1 ACHE 4708/4885RXRB 550/4885RXRA 440/4885
US-20030130370-A1 Photoinitiators for acrylic esters; reacting an acyl halide with a metal benzoyl phosphine; cable coatings, screen printing stencils, resist materials, colour filters, electrical encapsulation SMARCC1, ARPC5L, DHCR24 ACHE 4598/4885RXRB 2536/4885RXRA 2093/4885
US-20020026049-A1 Photoinitiators for acrylate coatings DHCR24, NR5A1, NR2C2 ACHE 4557/4885RXRB 1585/4885RXRA 1279/4885

“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.