Aldicarb

Aldicarb

SCHEMBL214691

CNC(=O)O/N=C/C(C)(C)SC.NC(CC(=O)O)C(=O)O

nearest known ligand 0.68

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2SLC6A3

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

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.68
ALDH1A1 P00352 1/20 0.42
TSHR P16473 1/20 0.42
HSD17B10 Q99714 1/20 0.42
GRIK1 P39086 5/20 0.38
GRIK2 Q13002 3/20 0.32
BHMT Q93088 4/20 0.32
SLC1A1 P43005 1/20 0.31
CYP2C19 P33261 1/20 0.30
THPO P40225 1/20 0.30
NOS3 P29474 1/20 0.30
NOS1 P29475 1/20 0.30
NOS2 P35228 1/20 0.30
GRIA2 P42262 2/20 0.30
GRIA4 P48058 2/20 0.30
GRIK3 Q13003 2/20 0.30
GRIK5 Q16478 2/20 0.30
GRIA1 P42261 1/20 0.30

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
Aldicarb SCHEMBL20568578 0.88 TDP1 (0.64) TDP1ALDH1A1TSHRHSD17B10GRIK1
Cystine SCHEMBL14645188 0.88 TDP1 (0.68) TDP1ALDH1A1TSHRHSD17B10GRIK1
Aldicarb SCHEMBL10933284 0.88 TDP1 (0.68) TDP1ALDH1A1TSHRHSD17B10GRIK1
Aldicarb SCHEMBL8778632 0.84 TDP1 (0.63) TDP1ALDH1A1TSHRHSD17B10CYP2C19
Aldicarb SCHEMBL21327721 0.84 TDP1 (0.90) TDP1ALDH1A1TSHRHSD17B10
Aldicarb SCHEMBL4061104 0.82 TDP1 (1.00) TDP1ALDH1A1TSHRHSD17B10
Aldicarb SCHEMBL9781 0.82 TDP1 (1.00) TDP1ALDH1A1TSHRHSD17B10
Aldicarb SCHEMBL7626286 0.82 TDP1 (1.00) TDP1ALDH1A1TSHRHSD17B10
Aldicarb SCHEMBL7864399 0.82 TDP1 (1.00) TDP1ALDH1A1TSHRHSD17B10
Aldicarb SCHEMBL7864397 0.82 TDP1 (1.00) TDP1ALDH1A1TSHRHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112779303-A Method for synthesizing orotic acid by biological enzyme method 华东理工大学 2021-05-11 CN claimed
EP-4687871-A1 TOPICAL PALA THERAPY FOR CANCER The Cleveland Clinic Foundation (US) 2026-02-11 EP disclosed
CN-119286751-B Genetically engineered bacterium for producing uridine diphosphate glucose, construction method and application thereof 诸城市浩天药业有限公司 2025-03-18 CN disclosed
CN-119391619-A Engineering strain for producing uridine diphosphate, construction method and method for synthesizing rebaudioside M 诸城市浩天药业有限公司 2025-02-07 CN disclosed
CN-119286751-A Genetically engineered bacterium for producing uridine diphosphate glucose, construction method and application thereof 诸城市浩天药业有限公司 2025-01-10 CN disclosed
WO-2024206402-A1 TOPICAL PALA THERAPY FOR CANCER THE CLEVELAND CLINIC FOUNDATION (US) 2024-10-03 WO disclosed
CN-112779303-B Method for synthesizing orotic acid by biological enzyme method 华东理工大学 2023-05-02 CN disclosed
CN-112779303-A Method for synthesizing orotic acid by biological enzyme method 华东理工大学 2021-05-11 CN disclosed
US-20150238472-A1 Dimethylarginine Dimethylaminohydrolase Inhibitors and Methods of Use Thereof THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2015-08-27 US disclosed
US-9011882-B2 Dimethylarginine dimethylaminohydrolase inhibitors and methods of use thereof THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2015-04-21 US disclosed
US-20030166615-A1 Protein kinase and phosphatase inhibitors and methods for designing them RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK, THE 2003-09-04 US disclosed
US-20030148311-A1 Aspartate carbamyltransferase as herbicidal target BASF AKTIENGESELLSCHAFT (DE) 2003-08-07 US disclosed
WO-2003035621-A1 PROTEIN KINASE AND PHOSPHATASE INHIBITORS, METHODS FOR DESIGNING THEM, AND METHODS OF USING THEM THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2003-05-01 WO disclosed
EP-1147214-A1 A NOVEL METHOD FOR DESIGNING PROTEIN KINASE INHIBITORS THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2001-10-24 EP disclosed
WO-2000042213-A1 A NOVEL METHOD FOR DESIGNING PROTEIN KINASE INHIBITORS THE RESEARCH FOUNDATION OF STATE UNIVERSITY OF NEW YORK (US) 2000-07-20 WO disclosed
EP-0458070-A1 Cytidine analogue resistance gene DNA and its use Takeda Chemical Industries, Ltd. (JP) 1991-11-27 EP disclosed
US-5041542-A Antitumor-anticarcinogenic agents NUCLEIC ACID RESEARCH INSTITUTE (US) 1991-08-20 US disclosed
US-4873228-A 2-oxo-4-carboxy-pyrimidines and their use as anti-malaria and anti-cancer agents THE UNIVERSITY OF MELBOURNE (AU) 1989-10-10 US disclosed
EP-0260057-A2 2-Oxo-4-carboxy-pyrimidines THE UNIVERSITY OF MELBOURNE (AU) 1988-03-16 EP disclosed
US-4550186-A ANTITUMOR, ANTILIPEMIC, ANTIINFLAMMATORY, AND ANTIARTHRITIC AGENTS DUKE UNIVERSITY (US) 1985-10-29 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 (2 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-20150238472-A1 Dimethylarginine Dimethylaminohydrolase Inhibitors and Methods of Use Thereof DDAH1, DIMT1, PADI1 TDP1 191/4885ALDH1A1 563/4885TSHR 3201/4885
US-20030166615-A1 Protein kinase and phosphatase inhibitors and methods for designing them PTPN5, PTPN2, PTPN6 TDP1 1604/4885ALDH1A1 4555/4885TSHR 2856/4885

“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.