Alpha-Phenyl-Gamma-Butyrolactone

Alpha-Phenyl-Gamma-Butyrolactone

SCHEMBL576473

O=C1OCCC1c1ccccc1

nearest known ligand 0.47

Full drug profile on Sugi Atlas →

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
CYP19A1 P11511 4/20 0.44
DDB1 Q16531 1/20 0.43
CRBN Q96SW2 1/20 0.43
CTRB1 P17538 1/20 0.41
CTRC Q99895 1/20 0.40
TSHR P16473 2/20 0.39
CFTR P13569 1/20 0.39
GOPC Q9HD26 1/20 0.39
KMT2A Q03164 1/20 0.39
MAPK1 P28482 1/20 0.39

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
Alpha-Phenyl-Gamma-Butyrolactone SCHEMBL7909086 1.00 CYP19A1 (0.44) CYP19A1DDB1CRBNCTRB1CTRC
Alpha-Phenyl-Gamma-Butyrolactone SCHEMBL6771142 1.00 CYP19A1 (0.44) CYP19A1DDB1CRBNCTRB1CTRC
Alpha-Phenyl-Gamma-Butyrolactone SCHEMBL28579210 0.91 CYP19A1 (0.40) CYP19A1DDB1CRBNCTRB1CTRC
SCHEMBL576991 0.88 TP53 (0.42) CYP19A1DDB1CRBNCTRB1CTRC
SCHEMBL576404 0.86 TP53 (0.41) CYP19A1DDB1CRBNCTRB1CTRC
Alpha-Phenyl-Gamma-Butyrolactone SCHEMBL28588955 0.84 CYP19A1 (0.43) CYP19A1DDB1CRBNCTRB1
Alpha-Phenyl-Gamma-Butyrolactone SCHEMBL28591531 0.83 ALDH1A1 (0.51) CYP19A1DDB1CRBNCTRB1CTRC
SCHEMBL6461863 0.80 ALOX12 (0.45) CYP19A1KMT2AMAPK1
SCHEMBL10393997 0.80 TP53 (0.42) CYP19A1KMT2A
SCHEMBL576857 0.80 CYP19A1 (0.45) CYP19A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118580203-A Preparation method of 5-benzoyl dihydrofuran-2 (3H) -ketone and derivative thereof 阜阳师范大学 2024-09-03 CN claimed
CN-113088393-B Fenghua Yulu essence 江苏省农业科学院 2024-02-27 CN claimed
CN-107721956-B Benzobutyrolactone derivative, synthesis method and application thereof in preparing bactericide 西北农林科技大学 2021-02-12 CN claimed
US-20080311478-A1 Lithium Secondary Battery MITSUBISHI CHEMICAL CORPORATION (JP) 2008-12-18 US claimed
EP-1892789-A1 LITHIUM SECONDARY BATTERY Mitsubishi Chemical Corporation (JP) 2008-02-27 EP claimed
EP-4662204-A2 TELOMERASE INHIBITOR COMPOUNDS Geron Corporation (US) 2025-12-17 EP disclosed
US-20250302803-A1 ARYL-SUBSTITUTED ACETAMIDE AND PYRROLIDIN-2-ONE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF SEIZURES UNIVERSITY OF HOUSTON SYSTEM (US) 2025-10-02 US disclosed
US-12357610-B2 Aryl-substituted acetamide and pyrrolidin-2-one derivatives and their use for the treatment of seizures UNIVERSITY OF HOUSTON SYSTEM (US) 2025-07-15 US disclosed
US-20240343713-A1 TELOMERASE INHIBITOR COMPOUNDS BIOPHARMA CREDIT PLC [COLLATERAL AGENT] (GB) 2024-10-17 US disclosed
WO-2024168165-A2 TELOMERASE INHIBITOR COMPOUNDS GERON CORPORATION (US) 2024-08-15 WO disclosed
US-20230414566-A1 ARYL-SUBSTITUTED ACETAMIDE AND PYRROLIDIN-2-ONE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF SEIZURES UNIVERSITY OF HOUSTON SYSTEM (US) 2023-12-28 US disclosed
US-11806333-B2 Aryl-substituted acetamide and pyrrolidin-2-one derivatives and their use for the treatment of seizures UNIVERSITY OF HOUSTON SYSTEM (US) 2023-11-07 US disclosed
WO-1994012487-A1 PROCESS FOR THE PREPARATION OF α-ARYL-η-BUTYROLACTONES JOHN WYETH & BROTHER LIMITED (GB) 1994-06-09 WO disclosed
EP-0400584-A2 Geminally substituted thiaheterocyclic carboxylic acids and derivatives thereof E.R. SQUIBB & SONS, INC. (US) 1990-12-05 EP disclosed
US-4975452-A Geminally substituted thiaheterocyclic carboxylic acids and derivatives thereof E. R. SQUIBB & SONS, INC. (US) 1990-12-04 US disclosed
US-4783473-A ANTICOAGULANTS, VASODILATORS, BRONCHODILATORS E. R. SQUIBB & SONS, INC. (US) 1988-11-08 US disclosed
EP-0107599-B1 PROCESS FOR THE PREPARATION OF SATURATED LINEAR ESTERS BY CARBONYLATION OF MONOOLEFINIC COMPOUNDS RHONE-POULENC CHIMIE DE BASE (FR) 1985-12-11 EP disclosed
EP-0107599-A1 Process for the preparation of saturated linear esters by carbonylation of monoolefinic compounds RHONE-POULENC CHIMIE DE BASE (FR) 1984-05-02 EP disclosed
US-4351839-A Fungicidal 2-aryl-2-1-H-azoyl-(alkyl)-gamma-butyrolactones ROHM AND HAAS COMPANY (US) 1982-09-28 US disclosed
US-3963757-A Process for the preparation of lactones PHILLIPS PETROLEUM COMPANY (US) 1976-06-15 US 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 (5 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-20240343713-A1 TELOMERASE INHIBITOR COMPOUNDS TERT, POT1, TERF2 CYP19A1 870/4885DDB1 194/4885CRBN 711/4885
US-12357610-B2 Aryl-substituted acetamide and pyrrolidin-2-one derivatives and their use for the treatment of seizures AADAC, GABRB2, GABARAPL2 CYP19A1 385/4885DDB1 2490/4885CRBN 2914/4885
US-20250302803-A1 ARYL-SUBSTITUTED ACETAMIDE AND PYRROLIDIN-2-ONE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF SEIZURES AADAC, GABRB2, GABARAPL2 CYP19A1 385/4885DDB1 2490/4885CRBN 2914/4885
US-20230414566-A1 ARYL-SUBSTITUTED ACETAMIDE AND PYRROLIDIN-2-ONE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF SEIZURES AADAC, GABRB2, GABARAPL2 CYP19A1 385/4885DDB1 2490/4885CRBN 2914/4885
US-11806333-B2 Aryl-substituted acetamide and pyrrolidin-2-one derivatives and their use for the treatment of seizures AADAC, GABRB2, GABARAPL2 CYP19A1 385/4885DDB1 2490/4885CRBN 2914/4885

“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.