Estriol

Estriol

SCHEMBL223226

C[C@]12CC[C@@H]3c4ccc(O)cc4CC[C@H]3[C@@H]1C[C@@H](O)[C@H]2O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ESR1ESR2

The experimentally established mechanism targets of Estriol. 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 known ✓ P03372 6/20 1.00
ESR2 known ✓ Q92731 5/20 1.00
LMNA P02545 3/20 1.00
SHBG P04278 3/20 1.00
CYP2C9 P11712 2/20 1.00
CYP2C19 P33261 2/20 1.00
HIF1A Q16665 2/20 1.00
NR3C1 P04150 2/20 1.00
PGR P06401 2/20 1.00
SERPINA6 P08185 2/20 1.00
AR P10275 2/20 1.00
SLC6A4 P31645 2/20 1.00
SNCA P37840 2/20 1.00
SLC6A3 Q01959 2/20 1.00
PTGS1 P23219 1/20 1.00
OR51E2 Q9H255 1/20 1.00
UGT1A10 Q9HAW8 1/20 1.00
HSD17B10 Q99714 3/20 0.72
TSHR P16473 2/20 0.72
STS P08842 2/20 0.72

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
Estriol SCHEMBL12180048 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL14373308 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL4896486 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL7004654 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL223196 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL13123063 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL23743979 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Epiestriol SCHEMBL221084 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL8941750 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9
Estriol SCHEMBL2001122 1.00 ESR1 (1.00) ESR1ESR2LMNASHBGCYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230089351-A1 METHODS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES Natural Extraction Systems, LLC (US) 2023-03-23 US claimed
WO-2022182523-A1 COMPOSITIONS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES Natural Extraction Systems, LLC (US) 2022-09-01 WO claimed
WO-2021158573-A1 METHODS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES Natural Extraction Systems, LLC (US) 2021-08-12 WO claimed
WO-2021158575-A1 COMPOSITIONS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES Natural Extraction Systems, LLC (US) 2021-08-12 WO claimed
US-20190180877-A1 ESTROGEN METABOLITE LEVELS AND CYP1B1 POLYMORPHISMS IN LUNG CANCER DIAGNOSIS, PROGNOSIS, AND RISK ASSESSMENT INSTITUTE FOR CANCER RESEARCH D/B/A THE RESEARCH INSTITUTE OF FOX CHASE CANCER CENTER 2019-06-13 US claimed
EP-2807482-B1 ANALYSIS OF ESTRADIOL AND ANALYTES WITH PHENOLIC OH USING LABELING CHEMISTRY AND LC-MSMS WORKFLOW DH TECHNOLOGIES DEV PTE LTD (SG) 2018-03-14 EP claimed
US-9874575-B2 Analysis of estradiol and analytes with phenolic OH using labeling chemistry and LC-MSMS workflow DH TECHNOLOGIES DEVELOPMENT PTE. LTD. (SG) 2018-01-23 US claimed
US-20150051111-A1 ANALYSIS OF ESTRADIOL AND ANALYTES WITH PHENOLIC OH USING LABELING CHEMISTRY AND LC-MSMS WORKFLOW DH TECHNOLOGIES DEVELOPMENT PTE. LTD. (SG) 2015-02-19 US claimed
US-20140363406-A1 ESTROGEN METABOLITE LEVELS AND CYP1B1 POLYMORPHISMS IN LUNG CANCER DIAGNOSIS, PROGNOSIS, AND RISK ASSESSMENT NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR 2014-12-11 US claimed
EP-2807482-A1 ANALYSIS OF ESTRADIOL AND ANALYTES WITH PHENOLIC OH USING LABELING CHEMISTRY AND LC-MSMS WORKFLOW Dh Technologies Development Pte. Ltd. (SG) 2014-12-03 EP claimed
WO-2012032529-A1 STEREOSELECTIVE REDUCTION OF ALPHA-HYDROXYKETONE RELIANCE LIFE SCIENCES PVT. LTD (IN) 2012-03-15 WO claimed
US-7951890-B2 Using epichlorohydrin to form gel; pulverization; mixing with buffer solution and hydrolases; stirring; centrifuging KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2011-05-31 US claimed
US-20100312137-A1 Ovulation Cycle Monitoring and Management GILMOUR ROBERT 2010-12-09 US claimed
US-20080207931-A1 Solid-Phase Extraction Method of Steroid Hormones by Entrapped Beta-Cyclodextrin Polymers KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2008-08-28 US claimed
EP-1952162-A2 OVULATION CYCLE MONITORING AND MANAGEMENT MANAWATU BIOTECH INVESTMENTS LTD. (MBIL) (NZ) 2008-08-06 EP claimed
WO-2007049157-A2 OVULATION CYCLE MONITORING AND MANAGEMENT MANAWATU BIOTECH INVESTMENTS LTD. (MBIL) (US) 2007-05-03 WO claimed
US-6476196-B1 Estrogen receptor ligands KARA BIO AB (SE) 2002-11-05 US claimed
EP-1149838-A1 Estriol substantially free of 16alpha, 17alpha-estra-1,3,5(10)-triene-3,16,17-triol AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.p.A. (IT) 2001-10-31 EP claimed
US-4592869-A Selective acylation process AKTIEBOLAGET LEO (SE) 1986-06-03 US claimed
EP-0138153-A2 A selective acylation process AB LEO (SE) 1985-04-24 EP claimed

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-20230089351-A1 METHODS RELATED TO BIOACTIVE AGENTS THAT CONVERT FROM ANIONS TO MOLECULES FABP2, FABP4, GUSB ESR1 1524/4885ESR2 409/4885LMNA 344/4885

“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.