Iodide

Iodide

SCHEMBL165638

I.c1ccc(P(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.92

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.33
TDP1 Q9NUW8 3/20 0.92
CYP3A4 P08684 1/20 0.92
ESR1 P03372 4/20 0.63
ESR2 Q92731 4/20 0.63
KDM4E B2RXH2 1/20 0.48
GAA P10253 1/20 0.48
ALDH1A1 P00352 4/20 0.38
NPSR1 Q6W5P4 1/20 0.37
DRD1 P21728 2/20 0.35
TSHR P16473 4/20 0.33
CA1 P00915 2/20 0.33
CA2 P00918 2/20 0.33
CA9 Q16790 2/20 0.33
LMNA P02545 2/20 0.33
CA12 O43570 1/20 0.33
GLA P06280 1/20 0.33
CA3 P07451 1/20 0.33
CA4 P22748 1/20 0.33
CA14 Q9ULX7 1/20 0.33

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
Iodide SCHEMBL28668485 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL525225 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL525223 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL3313118 1.00 TDP1 (0.92) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL11498883 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL5241027 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL10603415 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL809368 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Iodide SCHEMBL10825874 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E
Methane SCHEMBL7931585 0.96 TDP1 (0.86) TDP1CYP3A4ESR1ESR2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250215150-A1 CARBONATE-EPOXY COPOLYMER, CURABLE CARBONATE COMPOSITION, AND MANUFACTURING METHOD OF FORMING CARBONATE-CONTAINING THERMOSET Swancor Innovation & Incubation Co., Ltd. (TW) 2025-07-03 US claimed
EP-4578889-A1 CARBONATE-EPOXY COPOLYMER, CURABLE CARBONATE COMPOSITION, AND MANUFACTURING METHOD OF FORMING CARBONATE-CONTAINING THERMOSET Swancor Innovation & Incubation Co., Ltd. (TW) 2025-07-02 EP claimed
CN-119432196-A Breathable epoxy seal primer for concrete and preparation method thereof 长弢新材料(孝感)有限公司 2025-02-14 CN claimed
CN-113336717-B Process for preparing oxazolecarboxylic acid esters 江西天新药业股份有限公司 2024-04-05 CN claimed
CN-117486740-A Novel method for efficiently synthesizing chiral alpha-amino acid derivative by asymmetric reduction addition reaction of transition metal catalytic imine 华东理工大学 2024-02-02 CN claimed
CN-116041315-A Chemiluminescent probe for detecting Vanin-1 as well as preparation method and application thereof 中国药科大学 2023-05-02 CN claimed
CN-112079679-B Asymmetric total synthesis method of sex pheromone (R, Z) -21-methyl-8-thirty-five carbene of longicorn 塔里木大学 2022-10-11 CN claimed
CN-113336717-A Process for preparing oxazole carboxylic acid esters 江西天新药业股份有限公司 2021-09-03 CN claimed
CN-108559090-B Waterborne epoxy modified acrylic resin and preparation method thereof 中山大桥化工集团有限公司 2021-07-13 CN claimed
CN-104558008-B A kind of method for the intermediate for synthesizing paricalcitol 陕西师范大学 2017-12-05 CN claimed
EP-1072589-B1 Process for producing lycopene and intermediate thereof SUMITOMO CHEMICAL CO (JP) 2005-11-09 EP claimed
EP-1080082-B1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION NOVARTIS AG (CH) 2004-10-06 EP claimed
US-20030144523-A1 EPOTHILONE DERIVATIVES, METHOD FOR PRODUCING SAME AND THEIR PHARMACEUTICAL USE BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2003-07-31 US claimed
US-6350878-B1 BASIFICATION AND IODINATION OF ALDEHYDE NOVARTIS AG (CH) 2002-02-26 US claimed
US-6331652-B1 Process for producing lycopene and intermediate thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-12-18 US claimed
EP-1080082-A1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION Novartis AG (CH) 2001-03-07 EP claimed
EP-1072589-A2 Process for producing lycopene and intermediate thereof Sumitomo Chemical Company, Limited (JP) 2001-01-31 EP claimed
WO-1999059985-A1 INTERMEDIATES FOR THE SYNTHESIS OF EPOTHILONES AND METHODS FOR THEIR PREPARATION NOVARTIS AG (CH) 1999-11-25 WO claimed
EP-0835254-B1 OXAZOLIDINONE DERIVATIVES, THEIR PREPARATION AND THERAPEUTICAL USE SYNTHELABO (FR) 1999-09-01 EP claimed
US-5843975-A Oxazolidinone derivatives, their preparation and therapeutical use SYNTHELABO (FR) 1998-12-01 US 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-20030144523-A1 EPOTHILONE DERIVATIVES, METHOD FOR PRODUCING SAME AND THEIR PHARMACEUTICAL USE TUBB1, TUBA1C, TUBB4A ACHE 3927/4885TDP1 3303/4885CYP3A4 989/4885

“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.