Iobenguane

Iobenguane

SCHEMBL9798689

NC(N)=NCc1cccc(I)c1.O=S(=O)(O)O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

SLC6A2

The experimentally established mechanism targets of Iobenguane. 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
SLC6A2 known ✓ P23975 1/20 0.54
SMN1; SMN2 Q16637 3/20 1.00
LMNA P02545 1/20 1.00
PMP22 Q01453 1/20 1.00
CYP1A2 P05177 1/20 0.84
CYP2D6 P10635 1/20 0.84
CYP2C19 P33261 1/20 0.84
THPO P40225 1/20 0.84
RAB9A P51151 1/20 0.84
HIF1A Q16665 1/20 0.84
GRIN2B Q13224 6/20 0.61
GRIN2D O15399 2/20 0.61
GRIN3B O60391 2/20 0.61
GRIN1 Q05586 2/20 0.61
GRIN2A Q12879 2/20 0.61
GRIN2C Q14957 2/20 0.61
GRIN3A Q8TCU5 2/20 0.61
HTR3E A5X5Y0 2/20 0.60
HTR3B O95264 2/20 0.60
HTR3A P46098 2/20 0.60

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
Iobenguane SCHEMBL29722658 1.00 SMN1; SMN2 (1.00) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Iobenguane SCHEMBL29435410 1.00 SMN1; SMN2 (1.00) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Iobenguane SCHEMBL140592 0.92 CYP1A2 (1.00) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Iobenguane SCHEMBL16040804 0.90 CYP1A2 (0.96) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Iobenguane I 123 SCHEMBL30040171 0.79 HTR1A (0.81) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Sulfuric Acid SCHEMBL4014387 0.79 LMNA (0.65) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
SCHEMBL3927834 0.75 HIF1A (0.69) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
Hydrochloric Acid SCHEMBL538276 0.74 HTR3E (0.96) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
M-Fluorobenzylguanidine SCHEMBL11882096 0.74 TAAR1 (0.60) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6
SCHEMBL4811258 0.73 LMNA (0.57) SMN1; SMN2LMNAPMP22CYP1A2CYP2D6

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5019323-A Radioactive drug KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTRE (SA) 1991-05-28 US claimed
US-20240024518-A1 CONTRAST AGENT AND PRECURSOR AND MANUFACTURING METHOD THEREOF INSTITUTE OF NUCLEAR ENERGY RESEARCH, ATOMIC ENERGY COUNCIL, EXECUTIVE YUAN (TW) 2024-01-25 US disclosed
US-9221029-B2 Automatic system for synthesizing 123I-MIBG and automatic device for synthesizing and dispensing 123I-MIBG comprising the same INSTITUTE OF NUCLEAR ENERGY RESEARCH ATOMIC ENERGY COUNCIL, EXECUTIVE YUAN (TW) 2015-12-29 US disclosed
US-20150056105-A1 AUTOMATIC SYSTEM FOR SYNTHESIZING 123I-MIBG AND AUTOMATIC DEVICE FOR SYNTHESIZING AND DISPENSING 123I-MIBG COMPRISING THE SAME INSTITUTE OF NUCLEAR ENERGY RESEARCH ATOMIC ENERGY COUNCIL, EXECUTIVE YUAN (TW) 2015-02-26 US disclosed
US-5021220-A Haluaromatic compound, water-soluble acid, copper salt acid-stable reducing agent MALLINCKRODT, INC. (US) 1991-06-04 US disclosed
US-5019323-A Radioactive drug KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTRE (SA) 1991-05-28 US disclosed
US-4942231-A CATALYTIC HALOGENATION IN THE PRESENCE OF A REDUCING AGENT AND ACID MEDIUM MALLINCKRODT, INC. (US) 1990-07-17 US disclosed
EP-0165630-B1 METHOD OF PREPARING A CHLORINATED, BROMINATED, RADIOBROMINATED, IODINATED AND/OR RADIOIODINATED, AROMATIC OR HETEROAROMATIC COMPOUND, AS WELL AS A KIT FOR PREPARING A DIAGNOSTIC COMPOSITION ON THE BASIS OF THIS COMPOUND MALLINCKRODT, INC.(a Missouri corporation) (US) 1989-10-18 EP disclosed
EP-0288284-A2 Method of producing iodine 124 and meta-iodobenzylguanidine containing iodine 124 KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTRE (SA) 1988-10-26 EP disclosed
US-4584187-A RADIOIODINATED METAIODOBENZYL GUANIDINE;DIAGNOSS AND TREASTMENT OF HEART, ADRENAL MEDULLA, TUMORS WIELAND DONALD M 1986-04-22 US disclosed
EP-0165630-A2 Method of preparing a chlorinated, brominated, radiobrominated, iodinated and/or radioiodinated, aromatic or heteroaromatic compound, as well as a kit for preparing a diagnostic composition on the basis of this compound MALLINCKRODT, INC.(a Missouri corporation) (US) 1985-12-27 EP 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-20150056105-A1 AUTOMATIC SYSTEM FOR SYNTHESIZING 123I-MIBG AND AUTOMATIC DEVICE FOR SYNTHESIZING AND DISPENSING 123I-MIBG COMPRISING THE SAME BPGM, POLG, PIK3CG SLC6A2 34/4885SMN1; SMN2 4285/4885LMNA 4883/4885
US-20240024518-A1 CONTRAST AGENT AND PRECURSOR AND MANUFACTURING METHOD THEREOF TNNT2, NPPA, VHL SLC6A2 10/4885SMN1; SMN2 98/4885LMNA 573/4885

“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.