SCHEMBL4149482

SCHEMBL4149482

CS(=O)(=O)O.CS(=O)(=O)O.OCCOCCOCCOCCOCCOCCOCCOCCO

nearest known ligand 0.61

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. 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
MEN1 O00255 5/20 0.61
KMT2A Q03164 5/20 0.61
TSHR P16473 4/20 0.56
MAPK1 P28482 2/20 0.56
THRB P10828 1/20 0.46
HTT P42858 1/20 0.46
MAPT P10636 1/20 0.46
ALDH1A1 P00352 3/20 0.46
APP P05067 3/20 0.34
USP2 O75604 3/20 0.33
EPHX2 P34913 1/20 0.33
LMNA P02545 2/20 0.32
KDM4E B2RXH2 1/20 0.32
MMP9 P14780 1/20 0.32
ALOX15 P16050 1/20 0.32
CA2 P00918 1/20 0.32
CYP3A4 P08684 1/20 0.31
CASP1 P29466 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
SLCO1B3 Q9NPD5 1/20 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
Pentaethylene Glycol SCHEMBL4148519 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
SCHEMBL4140373 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Triethylene Glycol SCHEMBL29198607 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Tetraethylene Glycol SCHEMBL7688400 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Triethylene Glycol SCHEMBL1627441 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Hexaethylene Glycol SCHEMBL4154184 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
SCHEMBL4143918 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Pentaethylene Glycol SCHEMBL28557049 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Tetraethylene Glycol SCHEMBL4143923 1.00 MEN1 (0.61) MEN1KMT2ATSHRMAPK1THRB
Di(Hydroxyethyl)Ether SCHEMBL1790189 0.97 TSHR (0.59) MEN1KMT2ATSHRMAPK1THRB

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
US-8710097-B2 Flavonoid dimers and methods of making and using such THE HONG KONG POLYTECHNIC UNIVERSITY (CN) 2014-04-29 US disclosed
US-20090197943-A1 Flavonoid Dimers and Methods of Making and Using Such THE HONG KONG POLYTECHNIC UNIVERSITY (CN) 2009-08-06 US disclosed
EP-2029568-A1 FLAVONOID DIMERS AND METHODS OF MAKING AND USING SUCH The Hong Kong Polytechnic University (CN) 2009-03-04 EP disclosed
WO-2007135592-A1 FLAVONOID DIMERS AND METHODS OF MAKING AND USING SUCH THE HONG KONG POLYTECHNIC UNIVERSITY (CN) 2007-11-29 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 (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-20090197943-A1 Flavonoid Dimers and Methods of Making and Using Such ABCB1, ABCC1, SLC47A2 MEN1 4528/4885KMT2A 3704/4885TSHR 4591/4885

“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.