Estramustine Phosphate

Estramustine Phosphate

SCHEMBL234749

C[C@]12CC[C@@H]3c4ccc(OC(=O)N(CCCl)CCCl)cc4CC[C@H]3[C@@H]1CC[C@@H]2OP(=O)(O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR2

The experimentally established mechanism targets of Estramustine Phosphate. 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
ESR1 P03372 5/20 1.00
ADORA3 P0DMS8 4/20 1.00
PTPN11 Q06124 2/20 1.00
INPPL1 O15357 1/20 1.00
PTPN1 P18031 1/20 1.00
DRD1 P21728 1/20 1.00
PTPN6 P29350 1/20 1.00
KDR P35968 1/20 1.00
RECQL P46063 2/20 0.76
BLM P54132 1/20 0.76
TDP1 Q9NUW8 1/20 0.66
MAPT P10636 4/20 0.59
CYP3A4 P08684 4/20 0.59
SMN1; SMN2 Q16637 3/20 0.59
TP53 P04637 3/20 0.59
KMT2A Q03164 5/20 0.59
MEN1 O00255 4/20 0.59
THRB P10828 1/20 0.59
LMNA P02545 4/20 0.54
ATM Q13315 2/20 0.54

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
Estramustine Phosphate SCHEMBL13545664 1.00 ESR1 (1.00) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine Phosphate SCHEMBL1649356 1.00 ESR1 (1.00) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine Phosphate SCHEMBL29379408 1.00 ESR1 (1.00) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine Phosphate SCHEMBL19436 0.93 ESR1 (0.86) ESR1ADORA3PTPN11INPPL1PTPN1
SCHEMBL18775356 0.89 ESR1 (0.79) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine SCHEMBL3625800 0.88 RECQL (0.93) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine SCHEMBL36761 0.88 RECQL (0.93) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine SCHEMBL8342744 0.88 RECQL (0.93) ESR1ADORA3PTPN11INPPL1PTPN1
Estramustine SCHEMBL22129748 0.88 RECQL (0.93) ESR1ADORA3PTPN11INPPL1PTPN1
SCHEMBL13545743 0.88 ESR1 (0.78) ESR1ADORA3PTPN11INPPL1PTPN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3439640-B1 NANOPARTICLES FOR DRUG DELIVERY TO TREAT BONE DISEASE CLEVELAND CLINIC FOUND (US) 2024-01-17 EP disclosed
EP-3471712-B1 SMALL MOLECULE INHIBITORS OF ALDH AND USES THEREOF UNIV MICHIGAN REGENTS (US) 2024-01-03 EP disclosed
EP-3285583-B1 SMALL MOLECULE INHIBITORS OF MCL-1 AND USES THEREOF UNIV MICHIGAN REGENTS (US) 2021-03-17 EP disclosed
US-20200338202-A1 SHORT TAT OLIGOMERS FOR DRUG DELIVERY THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK 2020-10-29 US disclosed
EP-3125884-B1 SMALL MOLECULE INHIBITORS OF MCL-1 AND USES THEREOF UNIV MICHIGAN REGENTS (US) 2019-11-06 EP disclosed
WO-2019005754-A1 CANCER TREATMENT THE CLEVELAND CLINIC FOUNDATION (US) 2019-01-03 WO disclosed
EP-3131544-B1 MDM2 INHIBITORS AND THERAPEUTIC METHODS USING THE SAME UNIV MICHIGAN REGENTS (US) 2018-12-12 EP disclosed
WO-2018081719-A1 SMALL MOLECULE INHIBITORS OF NEK2 AND USES THEREOF ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2018-05-03 WO disclosed
EP-2911748-B1 CANCER STEM CELL VACCINATION AND TREATMENT UNIV MICHIGAN REGENTS (US) 2018-03-14 EP disclosed
EP-2831067-B1 SMALL MOLECULE INHIBITORS OF MCL-1 AND USES THEREOF UNIV MICHIGAN REGENTS (US) 2017-11-01 EP disclosed
EP-2141173-B1 Methods and compositions for the inhibition of gene expression PRONAI THERAPEUTICS INC (US) 2013-01-02 EP disclosed
US-8163805-B2 Small molecule antagonists of Bcl-2 family proteins THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2012-04-24 US disclosed
EP-1718767-B1 COMPOSITIONS FOR TREATING BREAST AND PANCREATIC CANCER UNIV MICHIGAN (US) 2012-04-11 EP disclosed
US-20120003150-A1 THERAPEUTIC RIBONUCLEASES QUINTESSENCE BIOSCIENCES, INC. (US) 2012-01-05 US disclosed
US-8088931-B2 Small molecule inhibitors of MDM2 and the uses thereof THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2012-01-03 US disclosed
EP-2369014-A1 Compositions and methods for characterizing, regulating, diagnosing and treating cancer The Regents Of The University Of Michigan Office Of Technology Transfer (US) 2011-09-28 EP disclosed
US-20110135710-A1 Methods and Compositions for the Inhibition of Gene Expression PRONAI THERAPEUTICS, INC. (US) 2011-06-09 US disclosed
US-7932382-B2 Amide substituted heterocylic compound; anticarcinogen; inducing apoptotic cell death, sensitizing cells to inducers of apoptosis THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2011-04-26 US disclosed
US-20110092452-A1 COMPOSITIONS AND METHODS FOR DIAGNOSING AND TREATING PANCREATIC CANCER THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2011-04-21 US disclosed
EP-2141173-A1 Methods and compositions for the inhibition of gene expression Pronai Therapeutics, Inc. (US) 2010-01-06 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 (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-20200338202-A1 SHORT TAT OLIGOMERS FOR DRUG DELIVERY ACIN1, MYCBP, STAT3 ESR1 1401/4885ADORA3 3802/4885PTPN11 4230/4885

“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.