Dexibuprofen

Dexibuprofen

SCHEMBL875767

CC(C)Cc1ccc([C@H](C)C(=O)O)cc1.NCCCCC(N)C(=O)O

nearest known ligand 0.73

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Dexibuprofen. 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 5/20 0.66
PTGS2 known ✓ P35354 5/20 0.66
THRB P10828 1/20 0.73
CXCR1 P25024 3/20 0.66
CXCR2 P25025 3/20 0.66
LMNA P02545 2/20 0.66
CYP2C9 P11712 2/20 0.66
AKR1C3 P42330 2/20 0.66
ALOX5 P09917 2/20 0.66
ALB P02768 1/20 0.66
ESR1 P03372 1/20 0.66
RARB P10826 1/20 0.66
ADRB3 P13945 1/20 0.66
NFKB1 P19838 1/20 0.66
HTR2A P28223 1/20 0.66
NR1I3 Q14994 1/20 0.66
SLC22A6 Q4U2R8 1/20 0.66
CXCL8 P10145 1/20 0.66
TSHR P16473 1/20 0.66
AKR1C2 P52895 1/20 0.66

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
Dexibuprofen SCHEMBL8733957 1.00 THRB (0.73) THRBPTGS1PTGS2CXCR1CXCR2
Ibuprofen SCHEMBL44617 1.00 THRB (0.73) THRBPTGS1PTGS2CXCR1CXCR2
(R)-Ibuprophen SCHEMBL29696062 1.00 THRB (0.73) THRBPTGS1PTGS2CXCR1CXCR2
(R)-Ibuprophen SCHEMBL8579043 1.00 THRB (0.73) THRBPTGS1PTGS2CXCR1CXCR2
Ibuprofen SCHEMBL44616 1.00 THRB (0.73) THRBPTGS1PTGS2CXCR1CXCR2
Ibuprofen SCHEMBL8902943 0.99 THRB (0.72) THRBPTGS1PTGS2CXCR1CXCR2
Ibuprofen SCHEMBL8902948 0.99 THRB (0.72) THRBPTGS1PTGS2CXCR1CXCR2
Dexibuprofen SCHEMBL379398 0.99 THRB (0.72) THRBPTGS1PTGS2CXCR1CXCR2
Lysine SCHEMBL11276603 0.92 THRB (0.71) THRBPTGS1PTGS2CXCR1CXCR2
Ibuprofen SCHEMBL20775003 0.86 PTGS1 (0.64) THRBPTGS1PTGS2CXCR1CXCR2

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 100 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230330032-A1 MICROENCAPSULATION PROCESS AND PRODUCT SPI PHARMA, INC. (US) 2023-10-19 US claimed
US-11723877-B2 Microencapsulation process and product SPI PHARMA, INC. (US) 2023-08-15 US claimed
EP-2629913-B1 MICROENCAPSULATION PROCESS AND PRODUCT SPI PHARMA INC (US) 2020-08-26 EP claimed
US-20200170959-A1 MICROENCAPSULATION PROCESS AND PRODUCT SPI PHARMA, INC. (US) 2020-06-04 US claimed
US-10561621-B2 Microencapsulation process and product SPI PHARMA, INC. 2020-02-18 US claimed
US-20140044793-A1 MICROENCAPSULATION PROCESS AND PRODUCT SPI PHARMA, INC. (US) 2014-02-13 US claimed
WO-2013175511-A1 TASTE MASKED PHARMACEUTICAL COMPOSITIONS V.B. MEDICARE PVT. LTD. (IN) 2013-11-28 WO claimed
EP-2629913-A1 MICROENCAPSULATION PROCESS AND PRODUCT SPI Pharma, INC. (US) 2013-08-28 EP claimed
WO-2013058496-A1 TASTE-MASKED PHARMACEUTICAL COMPOSITION FOR ORAL ADMINISTRATION AND A PROCESS FOR THE PREPARATION THEREOF DAEWOONG PHARMACEUTICAL CO., LTD. (KR) 2013-04-25 WO claimed
WO-2012040234-A1 MICROENCAPSULATION PROCESS AND PRODUCT SPI PHARMA, INC. (US) 2012-03-29 WO claimed
US-6551617-B1 The coating composition comprising polyvinyl acetate, a dimethylaminoethyl methacrylate, neutral methacrylic acid ester, and an alkaline modifier for enhancing the release of the active ingredient BRISTOL-MYERS SQUIBB COMPANY 2003-04-22 US claimed
EP-1276469-A2 TASTE MASKING COATING COMPOSITION Bristol-Myers Squibb Company (US) 2003-01-22 EP claimed
EP-1276470-A2 TASTE MASKING COATING COMPOSITION Bristol-Myers Squibb Company (US) 2003-01-22 EP claimed
US-20020197317-A1 Taste masking coating composition NOVARTIS AG (CH) 2002-12-26 US claimed
WO-2001080829-A2 TASTE MASKING COATING COMPOSITION BRISTOL-MYERS SQUIBB COMPANY (US) 2001-11-01 WO claimed
WO-2001080826-A2 TASTE MASKING COATING COMPOSITION BRISTOL-MYERS SQUIBB COMPANY (US) 2001-11-01 WO claimed
EP-0523847-B1 Taste mask coating for preparation of chewable pharmaceutical tablets MCNEIL PPC INC (US) 1996-04-24 EP claimed
US-5489436-A COATING WITH COPOLYMER OF DIMETHYLAMINOETHYL METHACRYLATEAND METHACRYLATE ESTER MCNEIL-PPC, INC. (US) 1996-02-06 US claimed
EP-0459695-B1 Taste masking and sustained release coatings for pharmaceuticals MCNEIL PPC INC (US) 1995-03-15 EP claimed
EP-0523847-A1 Taste mask coating for preparation of chewable pharmaceutical tablets McNEIL-PPC, INC. (US) 1993-01-20 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 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-20020197317-A1 Taste masking coating composition TAS2R45, TAS2R42, TAS2R60 PTGS1 3304/4885PTGS2 3542/4885THRB 1026/4885

“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.