SCHEMBL5043810

SCHEMBL5043810

Cc1cc(C)c(C(=O)P(=O)(C(=O)C(C)(C)C)c2ccccc2)c(C)c1

nearest known ligand 0.43

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.41
KDM4E B2RXH2 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
TSHR P16473 2/20 0.36
KMT2A Q03164 5/20 0.35
MEN1 O00255 4/20 0.35
ALDH1A1 P00352 2/20 0.35
GAA P10253 1/20 0.35
PKM P14618 1/20 0.35
SMN1; SMN2 Q16637 3/20 0.35
HTT P42858 3/20 0.35
HPGD P15428 1/20 0.34
MAPT P10636 2/20 0.34
CFTR P13569 1/20 0.33
NPC1 O15118 1/20 0.33
RAB9A P51151 1/20 0.33

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
SCHEMBL15158 0.89 LMNA (0.40) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
Iodide SCHEMBL29831346 0.87 LMNA (0.39) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
Ammonia Solution, Strong SCHEMBL28286046 0.87 LMNA (0.40) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
SCHEMBL28310329 0.87 LMNA (0.39) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
SCHEMBL30988127 0.87 KMT2A (0.41) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
SCHEMBL25250816 0.87 LMNA (0.39) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
Hydrogen Sulfide SCHEMBL28313413 0.87 LMNA (0.39) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
Lithium SCHEMBL30307090 0.87 LMNA (0.39) LMNAKMT2AMEN1ALDH1A1SMN1; SMN2
SCHEMBL7180182 0.87 LMNA (0.40) LMNAKDM4EL3MBTL1TSHRKMT2A
SCHEMBL7180487 0.84 LMNA (0.37) LMNAL3MBTL1KMT2AMEN1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105884809-A Preparing method for acyl phosphate (oxide) or sulfonyl phosphate (oxide) compound 郑成 2016-08-24 CN disclosed
CN-105884824-A Preparation method of acyl phosphine (oxygen) or sulfonyl phosphine (oxygen) compounds 郑成 2016-08-24 CN disclosed
US-7439401-B2 Process for preparing acylphosphanes and derivatives thereof CIBA SPECIALTY CHEMICALS CORPORATION (US) 2008-10-21 US disclosed
US-7439401-B2 Process for preparing acylphosphanes and derivatives thereof CIBA SPECIALTY CHEMICALS CORPORATION (US) 2008-10-21 US disclosed
US-7439401-B2 Process for preparing acylphosphanes and derivatives thereof CIBA SPECIALTY CHEMICALS CORPORATION (US) 2008-10-21 US disclosed
US-20060247436-A1 Process for preparing acylphosphanes and derivatives thereof IGM GROUP B.V. (NL) 2006-11-02 US disclosed
EP-1648908-B1 PROCESS FOR PREPARING ACYLPHOSPHANES AND DERIVATIVES THEREOF CIBA SC HOLDING AG (CH) 2006-10-18 EP disclosed
EP-1648908-A1 PROCESS FOR PREPARING ACYLPHOSPHANES AND DERIVATIVES THEREOF Ciba SC Holding AG (CH) 2006-04-26 EP disclosed
WO-2005014605-A1 PROCESS FOR PREPARING ACYLPHOSPHANES AND DERIVATIVES THEREOF CIBA SPECIALTY CHEMICALS HOLDING INC. (CH) 2005-02-17 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-20060247436-A1 Process for preparing acylphosphanes and derivatives thereof PHOSPHO1, PLA2G2C, SGMS2 LMNA 705/4885KDM4E 4208/4885L3MBTL1 3294/4885

“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.