SCHEMBL5993465

SCHEMBL5993465

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

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BCL2L1 Q07817 1/20 0.37
TSHR P16473 5/20 0.33
LMNA P02545 5/20 0.33
CYP3A4 P08684 4/20 0.33
ALDH1A1 P00352 4/20 0.33
CA2 P00918 3/20 0.33
L3MBTL1 Q9Y468 2/20 0.33
MAPK1 P28482 2/20 0.33
HTT P42858 2/20 0.33
SMN1; SMN2 Q16637 2/20 0.33
POLB P06746 1/20 0.33
GLA P06280 1/20 0.33
ITGB1 P05556 1/20 0.32
ITGA4 P13612 1/20 0.32
MEN1 O00255 1/20 0.32
HPGD P15428 1/20 0.32
KMT2A Q03164 1/20 0.32
ATM Q13315 1/20 0.31
TDP1 Q9NUW8 1/20 0.31
TAS1R3 Q7RTX0 1/20 0.31

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
SCHEMBL5996570 0.90 BCL2L1 (0.38) BCL2L1TSHRLMNACYP3A4ALDH1A1
SCHEMBL5995874 0.86 BCL2L1 (0.33) BCL2L1TSHRLMNACYP3A4ALDH1A1
SCHEMBL6469414 0.84 BCL2L1 (0.39) BCL2L1TSHRLMNACYP3A4ALDH1A1
SCHEMBL5996351 0.84 TRPM8 (0.38) LMNAALDH1A1SMN1; SMN2POLBITGB1
SCHEMBL5994494 0.84 KMT2A (0.38) TSHRLMNAALDH1A1L3MBTL1MAPK1
SCHEMBL5994453 0.83 TRPM8 (0.44) LMNAALDH1A1SMN1; SMN2POLBITGB1
SCHEMBL5998109 0.82 TRPM8 (0.42) LMNASMN1; SMN2ITGB1ITGA4MEN1
SCHEMBL5996099 0.82 TRPM8 (0.42) LMNASMN1; SMN2ITGB1ITGA4MEN1
SCHEMBL5996037 0.82 TRPM8 (0.42) LMNASMN1; SMN2ITGB1ITGA4MEN1
SCHEMBL5994798 0.82 TRPM8 (0.42) LMNASMN1; SMN2ITGB1ITGA4MEN1

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 980/4885TSHR 1096/4885LMNA 763/4885
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 3117/4885TSHR 4029/4885LMNA 975/4885
US-20020026049-A1 Photoinitiators for acrylate coatings DHCR24, NR5A1, NR2C2 BCL2L1 1201/4885TSHR 1670/4885LMNA 848/4885

“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.