Oxyphenbutazone Anhydrous

Oxyphenbutazone Anhydrous

SCHEMBL3182776

CCCC[C@@H]1C(=O)N(c2ccccc2)N(c2ccc(O)cc2)C1=O.O

nearest known ligand 0.97

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Oxyphenbutazone Anhydrous. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS1 known ✓ P23219 2/20 0.97
LMNA P02545 3/20 0.97
RAB9A P51151 3/20 0.97
ALDH1A1 P00352 2/20 0.97
CYP3A4 P08684 2/20 0.97
MAPK1 P28482 2/20 0.97
CYP1A2 P05177 2/20 0.97
CYP2C9 P11712 2/20 0.97
CYP2C19 P33261 2/20 0.97
TP53 P04637 1/20 0.97
MAPT P10636 1/20 0.97
HPGD P15428 1/20 0.97
NAPRT Q6XQN6 1/20 0.97
ABCB11 O95342 1/20 0.48
KDM4E B2RXH2 2/20 0.43
PKM P14618 1/20 0.43
GRM2 Q14416 6/20 0.41
GAA P10253 2/20 0.39
NPC1 O15118 1/20 0.39
MEN1 O00255 1/20 0.38

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
Oxyphenbutazone Anhydrous SCHEMBL25854 1.00 LMNA (0.97) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL2525061 1.00 LMNA (0.97) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL1263243 0.99 LMNA (0.94) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL25856 0.99 LMNA (1.00) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL5316370 0.99 LMNA (1.00) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL25857 0.99 LMNA (1.00) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL11337449 0.99 LMNA (1.00) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL1263248 0.97 LMNA (0.97) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL28278628 0.96 LMNA (0.94) LMNARAB9AALDH1A1CYP3A4PTGS1
Oxyphenbutazone Anhydrous SCHEMBL5612853 0.94 LMNA (0.92) LMNARAB9AALDH1A1CYP3A4PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7663000-B2 cytosine suppressive antiinflammatory agents; viricides; immunomodulators A-VIRAL ASA (NO) 2010-02-16 US disclosed
US-20080287390-A1 Pyrazolidinol compounds A-VIRAL AS (NO) 2008-11-20 US disclosed
US-20080262068-A1 Method of Tonic Treatment With Oxyphenbutazone Derivatives A-VIRAL ASA (NO) 2008-10-23 US disclosed
US-20070155812-A1 Thio-substituted phenbutazone compounds as anti-inflammatory, anti-viral and immunomodulatory agents DEKKERS DAVID W C 2007-07-05 US disclosed
US-20070112072-A1 Quinoneimines of malonic acid diamides A-VIRAL ASA (NO) 2007-05-17 US disclosed
US-20070037772-A1 Pyrazolidinol compounds A-VIRAL AS (NO) 2007-02-15 US disclosed
EP-1750692-A2 METHOD OF TONIC TREATMENT WITH OXYPHENBUTAZONE DERIVATIVES A-Viral ASA (NO) 2007-02-14 EP disclosed
EP-1651212-A1 THIO-SUBSTITUTED PHENBUTAZONE COMPOUNDS AS ANTI-INFLAMMATORY, ANTI-VIRAL AND IMMUNOMODULATORY AGENTS A-Viral ASA (NO) 2006-05-03 EP disclosed
EP-1651203-A1 QUINONEIMINES OF MALONIC ACID DIAMIDES A-Viral ASA (NO) 2006-05-03 EP disclosed
EP-1194409-B1 PYRAZOLIDINOL COMPOUNDS VIRAL ASA A (NO) 2006-02-01 EP disclosed
WO-2005107748-A2 METHOD OF TONIC TREATMENT WITH OXYPHENBUTAZONE DERIVATIVES A-VIRAL ASA (NO) 2005-11-17 WO disclosed
WO-2005011679-A1 THIO-SUBSTITUTED PHENBUTAZONE COMPOUNDS AS ANTI-INFLAMMATORY, ANTI-VIRAL AND IMMUNOMODULATORY AGENTS A-VIRAL ASA (NO) 2005-02-10 WO disclosed
WO-2005011664-A1 QUINONEIMINES OF MALONIC ACID DIAMIDES A-VIRAL ASA (NO) 2005-02-10 WO disclosed
US-6852749-B1 Pyrazolidinol compounds A-VIRAL AS (NO) 2005-02-08 US disclosed
US-20040152751-A1 Pyrazolidinol compounds TJOTTA ENOK (NO) 2004-08-05 US disclosed
EP-1194409-A1 PYRAZOLIDINOL COMPOUNDS A-Viral AS (NO) 2002-04-10 EP disclosed
EP-1140075-A1 TREATMENT OF RETROVIRAL INFECTIONS WITH OXYPHENBUTAZONE A-Viral AS (NO) 2001-10-10 EP disclosed
WO-2001000585-A1 PYRAZOLIDINOL COMPOUNDS A-VIRAL AS (NO) 2001-01-04 WO disclosed
WO-2000038679-A1 TREATMENT OF RETROVIRAL INFECTIONS WITH OXYPHENBUTAZONE A-VIRAL AS (NO) 2000-07-06 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 (6 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-20080262068-A1 Method of Tonic Treatment With Oxyphenbutazone Derivatives HTT, NFATC1, BACH1 PTGS1 658/4885LMNA 3740/4885RAB9A 2878/4885
US-20080287390-A1 Pyrazolidinol compounds NOX5, TPMT, ICOS PTGS1 205/4885LMNA 4868/4885RAB9A 4507/4885
US-20070155812-A1 Thio-substituted phenbutazone compounds as anti-inflammatory, anti-viral and immunomodulatory agents MSR1, CD4, SSB PTGS1 23/4885LMNA 4693/4885RAB9A 4342/4885
US-20070037772-A1 Pyrazolidinol compounds NOX5, TPMT, ICOS PTGS1 205/4885LMNA 4868/4885RAB9A 4507/4885
US-20040152751-A1 Pyrazolidinol compounds NOX5, TPMT, ICOS PTGS1 205/4885LMNA 4868/4885RAB9A 4507/4885
US-20070112072-A1 Quinoneimines of malonic acid diamides SQOR, MDH2, ME3 PTGS1 846/4885LMNA 4608/4885RAB9A 1194/4885

“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.