Trifluoroacetic Acid

Trifluoroacetic Acid

SCHEMBL562497

CCCCCn1c2nc(Br)[nH]c2c(=O)n2c(Cc3ccncc3)nnc12.O=C(O)C(F)(F)F

nearest known ligand 0.38

Full drug profile on Sugi Atlas →

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.38
SMN1; SMN2 Q16637 2/20 0.38
ADORA2A P29274 5/20 0.37
PCK1 P35558 2/20 0.36
HTT P42858 3/20 0.35
KDM4E B2RXH2 2/20 0.35
LMNA P02545 2/20 0.35
HPGD P15428 2/20 0.35
TSHR P16473 2/20 0.35
NPSR1 Q6W5P4 2/20 0.35
USP2 O75604 1/20 0.35
POLB P06746 1/20 0.35
PKM P14618 1/20 0.35
ALOX15 P16050 1/20 0.35
ALOX12 P18054 1/20 0.35
HSD17B10 Q99714 1/20 0.33
ADORA3 P0DMS8 1/20 0.33
ADORA2B P29275 1/20 0.33
ADORA1 P30542 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
SCHEMBL2526241 0.92 ALDH1A1 (0.43) ALDH1A1SMN1; SMN2ADORA2APCK1HTT
Trifluoroacetic Acid SCHEMBL562271 0.90 ADORA2A (0.36) ALDH1A1SMN1; SMN2ADORA2APCK1KDM4E
Trifluoroacetic Acid SCHEMBL562117 0.88 ADORA2A (0.41) ALDH1A1SMN1; SMN2ADORA2APCK1KDM4E
Trifluoroacetic Acid SCHEMBL562126 0.87 RXFP1 (0.40) ALDH1A1SMN1; SMN2HTTKDM4ELMNA
SCHEMBL562758 0.86 ALDH1A1 (0.46) ALDH1A1SMN1; SMN2ADORA2ALMNAHPGD
Trifluoroacetic Acid SCHEMBL563343 0.85 TP53 (0.40) ALDH1A1SMN1; SMN2KDM4ENPSR1ADORA3
Trifluoroacetic Acid SCHEMBL562306 0.85 RXFP1 (0.37) ALDH1A1SMN1; SMN2ADORA2AHTTTSHR
Trifluoroacetic Acid SCHEMBL562785 0.85 ADORA2B (0.38) ALDH1A1SMN1; SMN2ADORA2ANPSR1ADORA3
Trifluoroacetic Acid SCHEMBL562689 0.85 ADORA2A (0.36) ALDH1A1SMN1; SMN2ADORA2APCK1ADORA3
Trifluoroacetic Acid SCHEMBL562225 0.84 ADORA2A (0.38) ALDH1A1SMN1; SMN2ADORA2APCK1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140371216-A1 PURINONE DERIVATIVES AS HM74A AGONISTS INCYTE CORPORATION (US) 2014-12-18 US disclosed
US-8703783-B2 Purinone derivatives as HM74A agonists INCYTE CORPORATION (US) 2014-04-22 US disclosed
US-20120035172-A1 Purinone Derivatives as HM74A Agonists INCYTE CORPORATION (US) 2012-02-09 US disclosed
US-8039478-B2 Purinone derivatives as HM74A agonists INCYTE CORPORATION (US) 2011-10-18 US disclosed
US-20090286774-A1 PURINONE DERIVATIVES AS HM74A AGONISTS INCYTE CORPORATION (US) 2009-11-19 US disclosed
EP-2044074-A2 PURINONE DERIVATIVES AS HM74A AGONISTS Incyte Corporation (US) 2009-04-08 EP disclosed
US-7511050-B2 hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors; avoiding adverse effects such as hepatotoxicity and cutaneous flushing; low dosage; 2-bromo-8-methyl-4-pentyl-1,4-dihydro-5H-[1,2,4]triazolo[5,1-i]purin-5-one; to treat cardiovascular disorders INCYTE CORPORATION (US) 2009-03-31 US disclosed
US-20080045554-A1 hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors; avoiding adverse effects such as hepatotoxicity and cutaneous flushing; low dosage; 2-bromo-8-methyl-4-pentyl-1,4-dihydro-5H-[1,2,4]triazolo[5,1-i]purin-5-one; to treat cardiovascular disorders INCYTE CORPORATION (US) 2008-02-21 US disclosed
WO-2007150025-A2 PURINONE DERIVATIVES AS HM74A AGONISTS INCYTE CORPORATION (US) 2007-12-27 WO 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-20140371216-A1 PURINONE DERIVATIVES AS HM74A AGONISTS GPR84, P2RY1, ADRA1A ALDH1A1 641/4885SMN1; SMN2 1165/4885ADORA2A 12/4885
US-20120035172-A1 Purinone Derivatives as HM74A Agonists GPR84, P2RY1, ADRA1A ALDH1A1 641/4885SMN1; SMN2 1165/4885ADORA2A 12/4885
US-20090286774-A1 PURINONE DERIVATIVES AS HM74A AGONISTS GPR84, P2RY1, ADRA1A ALDH1A1 641/4885SMN1; SMN2 1165/4885ADORA2A 12/4885
US-20080045554-A1 hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors; avoiding adverse effects such as hepatotoxicity and cutaneous flushing; low dosage; 2-bromo-8-methyl-4-pentyl-1,4-dihydro-5H-[1,2,4]triazolo[5,1-i]purin-5-one; to treat cardiovascular disorders HMGCR, LDLR, GPBAR1 ALDH1A1 181/4885SMN1; SMN2 4478/4885ADORA2A 24/4885

“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.