SCHEMBL23476

SCHEMBL23476

O=C(O)c1ccccc1I(=O)=O

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 6/20 0.59
ALOX15 P16050 1/20 0.59
CA12 O43570 3/20 0.50
CA1 P00915 3/20 0.50
CA2 P00918 3/20 0.50
CA4 P22748 3/20 0.50
CA7 P43166 3/20 0.50
CA9 Q16790 3/20 0.50
KDM4E B2RXH2 2/20 0.50
HPGD P15428 2/20 0.50
HMGB1 P09429 1/20 0.50
CA6 P23280 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
NAPRT Q6XQN6 1/20 0.50
CA14 Q9ULX7 1/20 0.50
MAPT P10636 2/20 0.48
HDAC8 Q9BY41 1/20 0.48
POLB P06746 1/20 0.46
AKR1C3 P42330 1/20 0.46
NR4A1 P22736 1/20 0.45

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
SCHEMBL29517020 1.00 ALDH1A1 (0.59) ALDH1A1ALOX15CA12CA1CA2
Ammonia Solution, Strong SCHEMBL29433157 0.98 ALDH1A1 (0.56) ALDH1A1ALOX15CA12CA1CA2
SCHEMBL8522786 0.80 ALDH1A1 (0.46) ALDH1A1ALOX15CA12CA1CA2
SCHEMBL8523474 0.79 ALDH1A1 (0.52) ALDH1A1ALOX15KDM4EHPGDMAPT
Potassium Ion SCHEMBL8613656 0.77 ALDH1A1 (0.48) ALDH1A1ALOX15CA12CA1CA2
SCHEMBL8612213 0.77 ALDH1A1 (0.54) ALDH1A1ALOX15CA12CA1CA2
Phthalic Acid SCHEMBL1686043 0.76 ALDH1A1 (1.00) ALDH1A1ALOX15CA12CA1CA2
Phthalic Acid SCHEMBL146125 0.76 ALDH1A1 (1.00) ALDH1A1ALOX15CA12CA1CA2
Phthalic Acid SCHEMBL4452470 0.76 ALDH1A1 (1.00) ALDH1A1ALOX15CA12CA1CA2
Phthalic Acid SCHEMBL5668586 0.76 ALDH1A1 (1.00) ALDH1A1ALOX15CA12CA1CA2

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

Appears in 9410 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122080274-A Preparation method of functionalized polyolefin 2026-05-26 CN claimed
US-12641636-B2 Resource allocation method, device, and medium DATANG MOBILE COMMUNICATIONS EQUIPMENT CO., LTD. (CN) 2026-05-26 US claimed
US-12637439-B2 Preparation of cannabichromene and related cannabinoids BAYMEDICA, INC. (US) 2026-05-26 US claimed
CN-116813686-B Asymmetric synthesis method and application of 7-oxo-resorcinol lactone 欣凯医药化工中间体(上海)有限公司 2026-05-15 CN claimed
CN-122011071-A Synthesis method and application of DNA-ketoamide conjugate 重庆大学 2026-05-12 CN claimed
CN-115246867-B Method for synthesizing 7-ketolithocholic acid by taking BA as raw material 江苏佳尔科药业集团股份有限公司 2026-05-12 CN claimed
US-12590049-B2 Metal-free oxidation of pyrenes ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA (US) 2026-03-31 US claimed
US-12543103-B2 Access control method and apparatus, and communication device VIVO MOBILE COMMUNICATION CO., LTD. (CN) 2026-02-03 US claimed
EP-4683278-A1 COMMUNICATION METHOD, NETWORK DEVICE, TERMINAL DEVICE AND COMMUNICATION SYSTEM HUAWEI TECHNOLOGIES CO., LTD. (CN) 2026-01-21 EP claimed
WO-2025245089-A1 PROCESSES FOR PREPARING TETRALIN COMPOUNDS ARCUS BIOSCIENCES, INC. (US) 2025-11-27 WO claimed
CN-1071540-C Stabilization of aqueous 3-isothiazolone solutions ROHM & HAAS (US) 2001-09-26 CN claimed
WO-2001047945-A1 PROCESS FOR PREPARING 17ALPHA-ACETOXY-11BETA-[4-N,N-(DIMETHYLAMINO)PHENYL]-21-METHOXY-19-NORPREGNA-4,9-DIENE-3,20-DIONE, INTERMEDIATES USEFUL IN THE PROCESS, AND PROCESSES FOR PREPARING SUCH INTERMEDIATES THE GOVERNMENT OF THE UNITED STATES OF AMERICA, REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 2001-07-05 WO claimed
WO-2001014348-A1 FORMATION OF HETEROCYCLES THE SCRIPPS RESEARCH INSTITUTE (US) 2001-03-01 WO claimed
EP-0745326-B1 Stabilization of aqueous 3-isothiazolone solutions ROHM & HAAS (US) 1999-09-22 EP claimed
EP-0658533-B1 Process for the oxidation of primary and secondary alcohols to aldehydes and ketones and for the oxidation of 1,2-diols to alpha-ketols and alpha-diketones SIGMA TAU IND FARMACEUTI (IT) 1998-04-15 EP claimed
CN-1140542-A Stabilization of aqueous 3-isothiazolone solutions ROHM & HAAS (US) 1997-01-22 CN claimed
US-5594017-A WITH AN IODOSYL OR IODYL COMPOUND ROHM AND HAAS COMPANY (US) 1997-01-14 US claimed
EP-0745326-A1 Stabilization of aqueous 3-isothiazolone solutions ROHM AND HAAS COMPANY (US) 1996-12-04 EP claimed
US-5510538-A USING O-IODOXYBENZOIC ACID AS OXIDIZING AGENT SIGMA-TAU INDUSTRIE FARMACEUTICHE RIUNITE S.P.A. (IT) 1996-04-23 US claimed
EP-0658533-A1 Process for the oxidation of primary and secondary alcohols to aldehydes and ketones and for the oxidation of 1,2-diols to alpha-ketols and alpha-diketones Sigma-Tau Industrie Farmaceutiche Riunite S.p.A. (IT) 1995-06-21 EP claimed