SCHEMBL4186770

SCHEMBL4186770

OCCOC(CCO)COC(c1ccccc1)(c1ccccc1)c1ccccc1

nearest known ligand 0.44

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
DUT P33316 2/20 0.44
KIF11 P52732 1/20 0.42
PLA2G2A P14555 2/20 0.38
PLA2G10 O15496 1/20 0.38
PLA2G1B P04054 1/20 0.38
PLA2G5 P39877 1/20 0.38
TK1 P04183 2/20 0.36
CYP2C9 P11712 1/20 0.36
ALOX15 P16050 1/20 0.36
TSHR P16473 1/20 0.36
CYP2C19 P33261 1/20 0.36
ALDH1A1 P00352 1/20 0.34
RECQL P46063 1/20 0.34
SLC6A1 P30531 1/20 0.33
HRH4 Q9H3N8 1/20 0.32
PPARG P37231 1/20 0.31
NR1H2 P55055 1/20 0.31
NR1H3 Q13133 1/20 0.31
CTSK P43235 2/20 0.31

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
SCHEMBL4186763 1.00 DUT (0.44) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL26439425 0.93 PLA2G2A (0.42) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL4192561 0.85 DUT (0.39) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL4192567 0.85 DUT (0.39) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL13377619 0.84 DUT (0.41) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL8204874 0.84 DUT (0.39) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL5699551 0.83 DUT (0.40) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL4763266 0.83 DUT (0.40) DUTKIF11PLA2G2APLA2G10PLA2G1B
SCHEMBL8860746 0.81 CYP1A2 (0.36) DUTCYP2C9CYP2C19ALDH1A1RECQL
SCHEMBL4762320 0.81 DUT (0.39) DUTKIF11PLA2G2APLA2G10PLA2G1B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1341927-B1 METHOD OF PREPARING 3-¬2-{(METHYLSULFONYL)OXY}ETHOXY|-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG IND OHIO INC (US) 2006-08-02 EP claimed
EP-1341927-A1 METHOD OF PREPARING 3- 2- (METHYLSULFONYL)OXY ETHOXY]-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG Industries Ohio, Inc. (US) 2003-09-10 EP claimed
WO-2002059342-A1 METHOD OF PREPARING 3-[2-{(METHYLSULFONYL)OXY}ETHOXY]-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG INDUSTRIES OHIO, INC. (US) 2002-08-01 WO claimed
US-6300106-B1 FORMING S-ISOMER OR R-ISOMER OF (3,6-DIHYDRO-2H-PYRAN-2-YL)-METHANOL VIA A PROCESS WHICH PRODUCES A RACEMIC MIXTURE OF INTERMEDIATE REACTION PRODUCTS, RESOLVING TO SELECTIVELY PRODUCE S ISOMER PPG INDUSTRIES OHIO, INC. 2001-10-09 US claimed
US-20260042778-A1 Polymorphs of N-Desmethyl Ruboxistaurin and Salts Thereof 4M THERAPEUTICS INC. (US) 2026-02-12 US disclosed
EP-1061062-B1 PROCESS FOR PRODUCING BUTANETRIOL DERIVATIVES DAISO CO LTD (JP) 2009-02-18 EP disclosed
EP-1341927-B1 METHOD OF PREPARING 3-¬2-{(METHYLSULFONYL)OXY}ETHOXY|-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG IND OHIO INC (US) 2006-08-02 EP disclosed
US-20040024261-A1 Process for preparing butanetriol derivative DAISO CO., LTD. (JP) 2004-02-05 US disclosed
US-6620977-B1 Reacting 1,2,4-butanetriol in multiple steps with specified reagents using selective protection and deprotection of hydroxyl groups DAISO CO., LTD. (JP) 2003-09-16 US disclosed
EP-1341927-A1 METHOD OF PREPARING 3- 2- (METHYLSULFONYL)OXY ETHOXY]-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG Industries Ohio, Inc. (US) 2003-09-10 EP disclosed
WO-2002059342-A1 METHOD OF PREPARING 3-[2-{(METHYLSULFONYL)OXY}ETHOXY]-4-(TRIPHENYLMETHOXY)-1-BUTANOL, METHANE SULFONATE PPG INDUSTRIES OHIO, INC. (US) 2002-08-01 WO disclosed
US-6300106-B1 FORMING S-ISOMER OR R-ISOMER OF (3,6-DIHYDRO-2H-PYRAN-2-YL)-METHANOL VIA A PROCESS WHICH PRODUCES A RACEMIC MIXTURE OF INTERMEDIATE REACTION PRODUCTS, RESOLVING TO SELECTIVELY PRODUCE S ISOMER PPG INDUSTRIES OHIO, INC. 2001-10-09 US disclosed
US-5665877-A Synthesis of bisindolylmaleimides ELI LILLY AND COMPANY (US) 1997-09-09 US disclosed
EP-0776899-A1 Intermediates and their use to prepare N,N'-bridged bisindolylmaleimides ELI LILLY AND COMPANY (US) 1997-06-04 EP disclosed
EP-0776895-A1 Protein kinase C inhibitor ELI LILLY AND COMPANY (US) 1997-06-04 EP disclosed
WO-1997018809-A1 PROTEIN KINASE C INHIBITOR ELI LILLY AND COMPANY (US) 1997-05-29 WO disclosed
WO-1997019080-A1 NOVEL INTERMEDIATES AND THEIR USE TO PREPARE N,N'-BRIDGED BISINDOLYLMALEIMIDES ELI LILLY AND COMPANY (US) 1997-05-29 WO disclosed
US-5614647-A Intermediates for the synthesis of bisindolylmaleimides ELI LILLY AND COMPANY (US) 1997-03-25 US disclosed
US-5541347-A Synthesis of bisindolylmaleimides ELI LILLY AND COMPANY (US) 1996-07-30 US disclosed
EP-0657411-A1 Improved synthesis of bisindolylmaleimides ELI LILLY AND COMPANY (US) 1995-06-14 EP 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 (2 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-20260042778-A1 Polymorphs of N-Desmethyl Ruboxistaurin and Salts Thereof GSK3B, GSK3A, LRRK2 DUT 4665/4885KIF11 3811/4885PLA2G2A 4443/4885
US-20040024261-A1 Process for preparing butanetriol derivative CYP4B1, CYP11B2, CYP11B1 DUT 3136/4885KIF11 1774/4885PLA2G2A 4334/4885

“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.