SCHEMBL5996570

SCHEMBL5996570

CCCCC(CC)CP(=O)(CCCC)C(=O)c1c(C)cc(C)cc1C

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCL2L1 Q07817 1/20 0.38
CYP3A4 P08684 4/20 0.35
CA2 P00918 3/20 0.35
L3MBTL1 Q9Y468 2/20 0.35
ALDH1A1 P00352 4/20 0.35
TSHR P16473 5/20 0.34
LMNA P02545 5/20 0.34
MAPK1 P28482 2/20 0.34
HTT P42858 2/20 0.34
SMN1; SMN2 Q16637 2/20 0.34
POLB P06746 1/20 0.34
GLA P06280 1/20 0.34
MEN1 O00255 1/20 0.33
HPGD P15428 1/20 0.33
KMT2A Q03164 1/20 0.33
ITGB1 P05556 1/20 0.33
ITGA4 P13612 1/20 0.33
ATM Q13315 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
HSD17B10 Q99714 1/20 0.32

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
SCHEMBL5993465 0.90 BCL2L1 (0.37) BCL2L1CYP3A4CA2L3MBTL1ALDH1A1
SCHEMBL6469414 0.86 BCL2L1 (0.39) BCL2L1CYP3A4CA2L3MBTL1ALDH1A1
SCHEMBL5995874 0.84 BCL2L1 (0.33) BCL2L1CYP3A4CA2ALDH1A1TSHR
SCHEMBL5996351 0.83 TRPM8 (0.38) ALDH1A1LMNASMN1; SMN2POLBMEN1
SCHEMBL5995821 0.83 HPGD (0.41) L3MBTL1ALDH1A1TSHRLMNASMN1; SMN2
SCHEMBL7182831 0.80 ALDH1A1 (0.40) BCL2L1CYP3A4CA2L3MBTL1ALDH1A1
SCHEMBL5994231 0.80 HPGD (0.40) L3MBTL1ALDH1A1TSHRLMNASMN1; SMN2
SCHEMBL5993499 0.80 HPGD (0.40) ALDH1A1LMNASMN1; SMN2POLBMEN1
SCHEMBL5996449 0.80 HPGD (0.40) L3MBTL1ALDH1A1TSHRLMNASMN1; SMN2
SCHEMBL5994780 0.80 ALDH1A1 (0.36) ALDH1A1LMNASMN1; SMN2POLBMEN1

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 BCL2L1 980/4885CYP3A4 432/4885CA2 2861/4885
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 BCL2L1 3117/4885CYP3A4 2973/4885CA2 2987/4885
US-20020026049-A1 Photoinitiators for acrylate coatings DHCR24, NR5A1, NR2C2 BCL2L1 1201/4885CYP3A4 946/4885CA2 3313/4885

“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.