Phenylbutazone

Phenylbutazone

SCHEMBL7460714

CCCCC1C(=O)N(c2ccccc2)N(c2ccccc2)C1=O.CCCCOCCCC

nearest known ligand 0.70

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Phenylbutazone. 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 0.70
ALDH1A1 P00352 6/20 0.70
LMNA P02545 3/20 0.70
CYP3A4 P08684 2/20 0.70
HPGD P15428 2/20 0.70
CYP1A2 P05177 2/20 0.70
CYP2C9 P11712 2/20 0.70
CYP2C19 P33261 2/20 0.70
RAB9A P51151 2/20 0.70
MAPK1 P28482 1/20 0.70
TP53 P04637 1/20 0.70
MAPT P10636 1/20 0.70
NAPRT Q6XQN6 1/20 0.70
ABCB11 O95342 1/20 0.46
TSHR P16473 3/20 0.44
USP2 O75604 1/20 0.44
POLB P06746 1/20 0.44
ALOX15 P16050 1/20 0.44
HSD17B10 Q99714 1/20 0.44
NPY1R P25929 1/20 0.42

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
Phenylbutazone SCHEMBL8005041 0.91 RAB9A (0.82) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL3632 0.91 RAB9A (0.82) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL2874252 0.89 RAB9A (0.80) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL21694456 0.89 RAB9A (0.80) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL7715162 0.89 RAB9A (0.80) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL2122724 0.89 RAB9A (0.80) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL10913190 0.89 RAB9A (0.80) ALDH1A1LMNACYP3A4PTGS1HPGD
SCHEMBL4909796 0.86 CYP3A4 (0.71) ALDH1A1LMNACYP3A4PTGS1HPGD
SCHEMBL29489697 0.84 ALDH1A1 (0.73) ALDH1A1LMNACYP3A4PTGS1HPGD
Phenylbutazone SCHEMBL11269971 0.84 ALDH1A1 (0.72) ALDH1A1LMNACYP3A4PTGS1HPGD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1115751-A4 PHOTOPOLYMERIZATION PROCESS AND COMPOSITION EMPLOYING A CHARGE TRANSFER COMPLEX AND CATIONIC PHOTOINITIATOR FUSION UV SYS INC (US) 2002-08-14 EP disclosed
EP-1115751-A1 PHOTOPOLYMERIZATION PROCESS AND COMPOSITION EMPLOYING A CHARGE TRANSFER COMPLEX AND CATIONIC PHOTOINITIATOR Fusion Uv Systems, Inc. (US) 2001-07-18 EP disclosed
US-6127447-A RADIATION CURABLE COATING COMPOSITION INCLUDES AN EFFECTIVE AMOUNT OF CATIONIC PHOTOINITIATOR IN COMBINATION WITH A CHARGE TRANSFER COMPLEX FUSION UV SYSTEMS, INC. (US) 2000-10-03 US disclosed
WO-2000006613-A1 PHOTOPOLYMERIZATION PROCESS AND COMPOSITION EMPLOYING A CHARGE TRANSFER COMPLEX AND CATIONIC PHOTOINITIATOR FUSION UV SYSTEMS, INC. (US) 2000-02-10 WO disclosed