SCHEMBL349803

SCHEMBL349803

C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(OS(=O)(=O)O)ccc4[C@H]3CC[C@@]21C

nearest known ligand 0.78

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ESR1 P03372 5/20 0.78
CYP3A4 P08684 4/20 0.78
LMNA P02545 3/20 0.78
NR3C1 P04150 3/20 0.78
PGR P06401 3/20 0.78
SLC6A2 P23975 2/20 0.78
SLC6A4 P31645 2/20 0.78
SLC6A3 Q01959 2/20 0.78
CYP1A2 P05177 1/20 0.78
CYP2C19 P33261 1/20 0.78
HIF1A Q16665 1/20 0.78
CNR1 P21554 1/20 0.78
GAA P10253 1/20 0.73
MAPT P10636 1/20 0.73
MAPK1 P28482 1/20 0.73
ESR2 Q92731 2/20 0.71
ABCB11 O95342 2/20 0.71
SLC22A2 O15244 1/20 0.71
NR1I2 O75469 1/20 0.71
SHBG P04278 1/20 0.71

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
SCHEMBL17326003 1.00 ESR1 (0.78) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL19096138 0.91 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL17318121 0.91 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL4395173 0.91 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL19123270 0.91 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL6872679 0.91 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL7875926 0.90 ESR1 (0.72) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL4239106 0.90 ESR1 (0.72) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL8931573 0.90 ESR1 (0.74) ESR1CYP3A4LMNANR3C1PGR
SCHEMBL4389365 0.90 ESR1 (0.77) ESR1CYP3A4LMNANR3C1PGR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240123025-A1 LIPOPEPTIDES FOR USE IN TREATING LIVER DISEASES AND CARDIOVASCULAR DISEASES Ruprecht-Karls-Universität Heidelberg (DE) 2024-04-18 US claimed
US-20230346820-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF SARS-COV-2 THE SCRIPPS RESEARCH INSTITUTE 2023-11-02 US claimed
WO-2022144780-A1 SULFONAMIDE DERIVATIVES, COMPOSITIONS COMPRISING SAME AND USES THEREOF IN THE TREATMENT OF CANCERS NATIONAL CANCER CENTER (JP) 2022-07-07 WO claimed
US-9359451-B2 Methods and compositions for treating trauma-hemorrhage using estrogen and derivatives thereof THE UAB RESEARCH FOUNDATION (US) 2016-06-07 US claimed
US-20150352125-A1 Methods and Compositions for Treating Trauma-Hemorrhage Using Estrogen and Derivatives Thereof THE GOVERNMENT OF THE UNITED STATES, AS REPRESENTED BY THE SECRETARY OF THE ARMY 2015-12-10 US claimed
US-12622891-B2 AMP-activated protein kinase activator KYOTO PHARMACEUTICAL UNIVERSITY (JP) 2026-05-12 US disclosed
EP-3868384-B1 CYCLIC DINUCLEOTIDES AS STING (STIMULATOR OF INTERFERON GENES) AGONISTS TAKEDA PHARMACEUTICALS CO (JP) 2026-02-25 EP disclosed
US-20260022109-A1 5-HETEROARYL-1H-PYRAZOL-3-AMINE DERIVATIVE Sumitomo Pharma Co., Ltd. (JP) 2026-01-22 US disclosed
US-20260014080-A1 LIPOSOMAL PREPARATION WITH ENCAPSULATED HORMONES, METHOD OF PRODUCTION AND USE THEREOF VAN BOGAERT GINA (BE) 2026-01-15 US disclosed
US-12521358-B2 Method for selecting cancer patients for whom combination therapy with retinoid and cancer therapeutic agent is effective, and combination medicament with retinoid and cancer therapeutic agent RAQUALIA PHARMA INC. (JP) 2026-01-13 US disclosed
US-20250352541-A1 THERAPEUTIC FOR CANCER REFRACTORY TO IMMUNE CHECKPOINT INHIBITOR Sumitomo Pharma Co., Ltd. (JP) 2025-11-20 US disclosed
US-12447165-B2 Intratumoral vein-formation promoting agent OSAKA UNIVERSITY (JP) 2025-10-21 US disclosed
WO-2001030762-A1 IMIDAZOL-4-YLMETHANOLS USE AS INHIBITORS OF STEROID C17-20 LYASE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-05-03 WO disclosed
EP-1073640-A1 NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE Takeda Chemical Industries, Ltd. (JP) 2001-02-07 EP disclosed
EP-0974584-A1 FUSED RING COMPOUNDS, PROCESS FOR PRODUCING THE SAME AND USE THEREOF Takeda Chemical Industries, Ltd. (JP) 2000-01-26 EP disclosed
US-6015789-A LUTEINIZING HORMONE RELEASING HORMONE AGONIST AND A LUTEINIZING HORMONE RELEASING HORMONE ANTAGONIST IN COMBINATION, TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2000-01-18 US disclosed
WO-1999054309-A1 NAPHTHALENE DERIVATIVES, THEIR PRODUCTION AND USE TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1999-10-28 WO disclosed
EP-0906115-A1 COMBINED USE OF GnRH AGONIST AND ANTAGONIST Takeda Chemical Industries, Ltd. (JP) 1999-04-07 EP disclosed
EP-0819430-A1 Inhibitor of tumor metastasis or recurrence TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1998-01-21 EP disclosed
WO-1997040846-A1 COMBINED USE OF GnRH AGONIST AND ANTAGONIST TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1997-11-06 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 (6 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-20260014080-A1 LIPOSOMAL PREPARATION WITH ENCAPSULATED HORMONES, METHOD OF PRODUCTION AND USE THEREOF NR5A1, SHBG, GNRHR ESR1 188/4885CYP3A4 1458/4885LMNA 796/4885
US-12622891-B2 AMP-activated protein kinase activator PRKAA1, PRKAG1, PRKAB1 ESR1 3201/4885CYP3A4 4733/4885LMNA 2028/4885
US-20260022109-A1 5-HETEROARYL-1H-PYRAZOL-3-AMINE DERIVATIVE CHEK1, CHEK2, WEE1 ESR1 4066/4885CYP3A4 3135/4885LMNA 1378/4885
US-20230346820-A1 METHODS AND COMPOSITIONS FOR THE TREATMENT OF SARS-COV-2 ACE2, SARS1, ACE ESR1 3467/4885CYP3A4 752/4885LMNA 2675/4885
US-20150352125-A1 Methods and Compositions for Treating Trauma-Hemorrhage Using Estrogen and Derivatives Thereof SHBG, ESR1, ESR2 ESR1 2/4885CYP3A4 644/4885LMNA 466/4885
US-20250352541-A1 THERAPEUTIC FOR CANCER REFRACTORY TO IMMUNE CHECKPOINT INHIBITOR CHEK1, CHEK2, PDCD1 ESR1 3282/4885CYP3A4 4836/4885LMNA 3273/4885

“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.