SCHEMBL5994796

SCHEMBL5994796

CCP(=O)(C(=O)c1c(C)cc(C)cc1C)C(=O)c1c(OC)cc(C)cc1OC

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PKM P14618 1/20 0.38
SMN1; SMN2 Q16637 3/20 0.37
MEN1 O00255 3/20 0.37
KMT2A Q03164 3/20 0.37
HPGD P15428 2/20 0.37
LMNA P02545 1/20 0.37
ALDH1A1 P00352 2/20 0.36
GABRA1 P14867 1/20 0.36
GABRG2 P18507 1/20 0.36
GABRB3 P28472 1/20 0.36
ACHE P22303 1/20 0.35
CYP3A4 P08684 3/20 0.34
USP2 O75604 1/20 0.34
MAPK1 P28482 1/20 0.34
ERN1 O75460 1/20 0.34
CRHR1 P34998 1/20 0.34
TAS1R3 Q7RTX0 1/20 0.33
TAS1R1 Q7RTX1 1/20 0.33
TAS1R2 Q8TE23 1/20 0.33
POLB P06746 1/20 0.33

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
SCHEMBL5994583 0.94 CYP3A4 (0.42) PKMSMN1; SMN2MEN1KMT2AHPGD
SCHEMBL5996043 0.90 CNR2 (0.37) PKMSMN1; SMN2HPGDLMNAALDH1A1
SCHEMBL5996716 0.90 TAS1R3 (0.44) PKMMEN1KMT2AALDH1A1CYP3A4
SCHEMBL5997081 0.90 TAS1R3 (0.44) SMN1; SMN2MEN1KMT2ALMNAALDH1A1
SCHEMBL2499305 0.87 HPGD (0.45) SMN1; SMN2MEN1KMT2AHPGDLMNA
SCHEMBL5996764 0.87 CA12 (0.45) SMN1; SMN2ALDH1A1CYP3A4MAPK1TAS1R3
SCHEMBL5996261 0.86 ITGB1 (0.36) PKMSMN1; SMN2MEN1KMT2AHPGD
SCHEMBL5995448 0.84 PKM (0.38) PKMSMN1; SMN2MEN1KMT2AALDH1A1
SCHEMBL5993728 0.83 ELANE (0.38) SMN1; SMN2KMT2AHPGDLMNACYP3A4
SCHEMBL5995274 0.83 HDAC3 (0.45) PKMSMN1; SMN2MEN1KMT2AHPGD

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 PKM 4644/4885SMN1; SMN2 3940/4885MEN1 3862/4885
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 PKM 4235/4885SMN1; SMN2 1663/4885MEN1 2456/4885
US-20020026049-A1 Photoinitiators for acrylate coatings DHCR24, NR5A1, NR2C2 PKM 4829/4885SMN1; SMN2 4099/4885MEN1 3695/4885

“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.