Diatrizoic Acid

Diatrizoic Acid

SCHEMBL4334352

CC(=O)Nc1c(I)c(NC(C)=O)c(I)c(C(=O)O)c1I.CC(=O)Nc1c(I)c(NC(C)=O)c(I)c(C(=O)[O-])c1I.CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO.[Na+]

nearest known ligand 0.87

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TACR1TTRgyrAgyrBparCparE

The experimentally established mechanism targets of Diatrizoic Acid. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 1/20 0.87
LMNA P02545 4/20 0.56
KDM4E B2RXH2 2/20 0.42
CYP1A2 P05177 1/20 0.31
TSHR P16473 1/20 0.31
HIF1A Q16665 1/20 0.31

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
Diatrizoic Acid SCHEMBL4728330 0.95 SMN1; SMN2 (0.78) SMN1; SMN2LMNAKDM4E
Diatrizoic Acid SCHEMBL2501947 0.94 SMN1; SMN2 (0.97) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Diatrizoic Acid SCHEMBL720469 0.93 SMN1; SMN2 (1.00) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Diatrizoic Acid SCHEMBL1685085 0.93 SMN1; SMN2 (1.00) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Diatrizoic Acid SCHEMBL107036 0.93 SMN1; SMN2 (1.00) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Diatrizoic Acid SCHEMBL468613 0.92 SMN1; SMN2 (0.97) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Iothalamic Acid SCHEMBL29488709 0.85 SMN1; SMN2 (0.84) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Iothalamic Acid SCHEMBL180546 0.85 SMN1; SMN2 (0.84) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Iothalamic Acid SCHEMBL48785 0.85 SMN1; SMN2 (0.84) SMN1; SMN2LMNAKDM4ECYP1A2TSHR
Iothalamic Acid SCHEMBL3060866 0.84 SMN1; SMN2 (0.83) SMN1; SMN2LMNAKDM4ECYP1A2TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4732418-A2 DISCHARGE CONTROL FOR POWER PROCESSING AND TIME-VARYING VOLTAGE PROFILE GENERATION The Regents Of The University Of Michigan (US) 2026-04-29 EP claimed
US-20250301329-A1 DEVICES AND METHODS FOR EMBEDDED SUBSCRIBER IDENTITY MODULE PROVISIONING HAND HELD PRODUCTS, INC. 2025-09-25 US claimed
EP-4622316-A1 DEVICES AND METHODS FOR EMBEDDED SUBSCRIBER IDENTITY MODULE PROVISIONING Hand Held Products, Inc. (US) 2025-09-24 EP claimed
EP-4543498-A2 COMPOSITION AND METHOD FOR DIAGNOSTIC IMAGING Suntec Medical, Inc. (US) 2025-04-30 EP claimed
US-20250121100-A1 COMPOSITION AND METHOD FOR DIAGNOSTIC IMAGING SUNTEC MEDICAL INC (US) 2025-04-17 US claimed
CN-119698306-A Compositions and methods for diagnostic imaging 欣扬生医股份有限公司 2025-03-25 CN claimed
WO-2024264049-A2 DISCHARGE CONTROL FOR POWER PROCESSING AND TIME-VARYING VOLTAGE PROFILE GENERATION THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2024-12-26 WO claimed
US-20240343483-A1 DEVICE AND METHOD FOR PLACING RACKS KIA CORPORATION (KR) 2024-10-17 US claimed
US-12053880-B2 Mobile robot platform BROETJE-AUTOMATION GMBH (DE) 2024-08-06 US claimed
CN-116094992-B Message forwarding method, storage medium and device based on worksheet scene 中电信数智科技有限公司 2024-04-16 CN claimed
CN-108535722-B Radar reference azimuth calibration device 中国人民解放军陆军炮兵防空兵学院郑州校区 2023-11-03 CN claimed
CN-115024839-B Orthodontic archwire error rate evaluation method based on normalized bending point angular distance ratio 哈尔滨理工大学 2023-10-27 CN claimed
WO-2023187235-A1 FOUNDATION FOR WIND GENERATOR TOWERS AND BUILDING METHOD OF SAID FOUNDATION MS TECHNO RDITECH SL (ES) 2023-10-05 WO claimed
CN-113839392-B Power grid reactive voltage robust optimization method considering distributed new energy random output 华北电力大学(保定) 2023-07-18 CN claimed
US-20230220487-A1 MOLECULAR MARKERS AND METHODS FOR SAMPLE ANALYSIS VIA MASS SPECTROMETRY BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2023-07-13 US claimed
WO-2023094450-A1 CONTROL SYSTEM AND METHOD FOR A VEHICLE USING POWERLINE COMMUNICATION, PLC. ZF FRIEDRICHSHAFEN AG (DE) 2023-06-01 WO claimed
CN-116094992-A Message forwarding method, storage medium and device based on worksheet scene 中电信数智科技有限公司 2023-05-09 CN claimed
WO-2022243964-A1 ARRANGEMENT OF ELECTRONIC ELEMENTS TO OPTIMIZE USER MANAGEMENT IN THE GAMING BET MARKET PINERO MAS ISRAEL (ES) 2022-11-24 WO claimed
US-20220188922-A1 SYSTEM AND METHOD OF PROVIDING A BENEFIT KASHABLE LLC (US) 2022-06-16 US claimed
CN-108537055-B Privacy budget allocation and data release method and system for data query privacy protection 南京邮电大学 2022-04-05 CN 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-20250121100-A1 COMPOSITION AND METHOD FOR DIAGNOSTIC IMAGING ABCB4, C5, APOB SMN1; SMN2 2359/4885LMNA 793/4885KDM4E 3929/4885

“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.