SCHEMBL5556172

SCHEMBL5556172

CCOC(=O)C(O)(CCC=C(C)C)CC(=O)OC1CCC[C@@H](C)[C@@H]1C(C)C

nearest known ligand 0.30

Predicted protein targets (top 2)

geneUniProtsupporting neighboursconfidence
GLA P06280 1/20 0.30
HPGD P15428 1/20 0.30

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
SCHEMBL5556173 0.80 CYP19A1 (0.41) HPGD
SCHEMBL13059722 0.80 CYP19A1 (0.41) HPGD
SCHEMBL7133227 0.80 CYP19A1 (0.41) HPGD
SCHEMBL1736059 0.72 ALOX15 (0.37)
SCHEMBL8713295 0.64 PKM (0.31)
SCHEMBL14624782 0.64 TSHR (0.36)
SCHEMBL4771757 0.62 EPHX1 (0.33)
SCHEMBL1536314 0.62 EPHX1 (0.33)
SCHEMBL14524046 0.62 CYP3A4 (0.34)
SCHEMBL28376231 0.62 TSHR (0.36)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7169774-B2 Cephalotaxane derivatives and their processes of preparation and purification STRAGEN PHARMA S.A. (CH) 2007-01-30 US disclosed
US-20060234999-A1 Cephalotaxane derivatives and their processes of preparation and purification TEVA PHARMACEUTICALS INTERNATIONAL GMBH (CH) 2006-10-19 US disclosed
US-20050090484-A1 Cephalotaxane derivatives and their processes of preparation and purification IVAX International GmbH (CH) 2005-04-28 US disclosed
EP-1064285-B1 NOVEL CEPHALOTAXANE DERIVATIVES AND PROCESS FOR THEIR PREPARATION STRAGEN PHARMA SA (CH) 2005-02-16 EP disclosed
US-6831180-B1 Substituted tertiary carboxylic oxacycloalkane acids, used to prepare anhydro-homo-harringtonic acids by semi-synthesis; hydroxyl function of a cephalotaxane is esterified with a 2-carboxyl-2-alkyl-1-oxacycloalkane claimed intermediate; (indexing from 7169774 added) STRAGEN PHARMA SA. (CH) 2004-12-14 US disclosed
US-6613900-B2 Asymetric hemisynthesis of harringtonines and their analogs, that are alkaloids used in chemotherapy. ONCOPHARM CORPORATION 2003-09-02 US disclosed
EP-1064285-A1 NOVEL CEPHALOTAXANE DERIVATIVES AND PROCESS FOR THEIR PREPARATION Oncopharm Corporation (US) 2001-01-03 EP disclosed
WO-1999048894-A1 NOVEL CEPHALOTAXANE DERIVATIVES AND PROCESS FOR THEIR PREPARATION ONCOPHARM CORPORATION (US) 1999-09-30 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 (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-20060234999-A1 Cephalotaxane derivatives and their processes of preparation and purification UGT1A7, CYP8B1, UGT2B7 GLA 3651/4885HPGD 2654/4885
US-20050090484-A1 Cephalotaxane derivatives and their processes of preparation and purification UGT1A7, CYP8B1, UGT2B7 GLA 3651/4885HPGD 2654/4885

“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.