Lisofylline

Lisofylline

SCHEMBL6879162

[2H]c1nc2c(c(=O)n(CCCC([2H])([2H])[C@H](C)O)c(=O)n2C)n1C([2H])([2H])[2H]

nearest known ligand 0.60

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADORA2B P29275 5/20 0.49
TNF P01375 4/20 0.49
LMNA P02545 3/20 0.49
SMN1; SMN2 Q16637 2/20 0.49
CYP1A2 P05177 2/20 0.49
NFKB1 P19838 2/20 0.49
ACHE P22303 2/20 0.49
PDE4A P27815 2/20 0.49
PMP22 Q01453 2/20 0.49
USP2 O75604 1/20 0.49
TSHR P16473 1/20 0.49
PDE4B Q07343 1/20 0.49
PDE4C Q08493 1/20 0.49
PDE4D Q08499 1/20 0.49
RXFP1 Q9HBX9 1/20 0.49
CHIT1 Q13231 1/20 0.42
CHIA Q9BZP6 1/20 0.42
AKR1B1 P15121 1/20 0.41
ESR1 P03372 1/20 0.41
MAPT P10636 1/20 0.41

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
Lisofylline SCHEMBL6878157 1.00 ADORA2B (0.49) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL6877081 1.00 ADORA2B (0.49) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL15340999 0.97 TNF (0.46) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL15423035 0.97 TNF (0.46) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL13695586 0.94 ADORA2B (0.48) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL13695587 0.94 ADORA2B (0.48) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL13695588 0.94 ADORA2B (0.48) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL6878416 0.94 ADORA2B (0.52) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL6877342 0.94 ADORA2B (0.52) ADORA2BTNFLMNASMN1; SMN2CYP1A2
Lisofylline SCHEMBL6877052 0.94 ADORA2B (0.52) ADORA2BTNFLMNASMN1; SMN2CYP1A2

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-20130280768-A1 PROCESS FOR PREPARING AN ENANTIOMERICALLY ENRICHED, DEUTERATED SECONDARY ALCOHOL FROM A CORRESPONDING KETONE WITHOUT REDUCING DEUTERIUM INCORPORATION CONCERT PHARMACEUTICALS, INC. (US) 2013-10-24 US disclosed
US-8263601-B2 Deuterium substituted xanthine derivatives CONCERT PHARMACEUTICALS, INC. (US) 2012-09-11 US disclosed
US-20120202830-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. 2012-08-09 US disclosed
US-20110077255-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. 2011-03-31 US disclosed
US-20110059995-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS INC. 2011-03-10 US disclosed
US-20110053961-A1 SUBSTITUTED XANTHINE DERIVATIVES CONCERT PHARMACEUTICALS, INC. 2011-03-03 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 (4 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-20110077255-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, HPRT1, CXCR3 ADORA2B 60/4885TNF 583/4885LMNA 2823/4885
US-20110053961-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, HPRT1, CXCR3 ADORA2B 60/4885TNF 583/4885LMNA 2823/4885
US-20120202830-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, HPRT1, CXCR3 ADORA2B 60/4885TNF 583/4885LMNA 2823/4885
US-20110059995-A1 SUBSTITUTED XANTHINE DERIVATIVES XDH, HPRT1, CXCR3 ADORA2B 60/4885TNF 583/4885LMNA 2823/4885

“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.