Iodide

Iodide

SCHEMBL336205

Cc1nc2ccccc2n1C.I

nearest known ligand 0.61

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
SMN1; SMN2 Q16637 5/20 0.61
KDM4E B2RXH2 9/20 0.60
ALDH1A1 P00352 6/20 0.60
LMNA P02545 3/20 0.60
ATM Q13315 1/20 0.57
MAPK1 P28482 2/20 0.55
HTT P42858 1/20 0.55
MEN1 O00255 2/20 0.55
KMT2A Q03164 2/20 0.55
NPC1 O15118 4/20 0.53
RAB9A P51151 4/20 0.53
TP53 P04637 3/20 0.53
HSD17B10 Q99714 3/20 0.53
GAA P10253 2/20 0.53
PKM P14618 2/20 0.53
ALOX15 P16050 1/20 0.53
TSHR P16473 1/20 0.52
MAPT P10636 2/20 0.51
HPGD P15428 2/20 0.51
CYP3A4 P08684 1/20 0.50

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 SCHEMBL336206 1.00 SMN1; SMN2 (0.61) SMN1; SMN2KDM4EALDH1A1LMNAATM
Iodide SCHEMBL27898886 1.00 SMN1; SMN2 (0.61) SMN1; SMN2KDM4EALDH1A1LMNAATM
SCHEMBL353890 0.98 SMN1; SMN2 (0.63) SMN1; SMN2KDM4EALDH1A1LMNAATM
Bromide SCHEMBL5318089 0.96 SMN1; SMN2 (0.61) SMN1; SMN2KDM4EALDH1A1LMNAATM
Ammonia Solution, Strong SCHEMBL19182582 0.96 SMN1; SMN2 (0.61) SMN1; SMN2KDM4EALDH1A1LMNAATM
Hydrochloric Acid SCHEMBL20291495 0.94 SMN1; SMN2 (0.59) SMN1; SMN2KDM4EALDH1A1LMNAATM
Formamide SCHEMBL17938372 0.87 SMN1; SMN2 (0.52) SMN1; SMN2KDM4EALDH1A1LMNAATM
SCHEMBL27562084 0.87 SMN1; SMN2 (0.52) SMN1; SMN2KDM4EALDH1A1LMNAATM
SCHEMBL1171430 0.82 MEN1 (0.69) SMN1; SMN2KDM4EALDH1A1LMNAATM
SCHEMBL29354143 0.82 ALDH1A1 (0.50) SMN1; SMN2KDM4EALDH1A1LMNAATM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8097756-B2 Process for producing carboxylic acid anhydrides CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2012-01-17 US claimed
US-20100145098-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ANHYDRIDES CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2010-06-10 US claimed
US-8097756-B2 Process for producing carboxylic acid anhydrides CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2012-01-17 US disclosed
US-20100145098-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ANHYDRIDES CHINA PETROCHEMICAL DEVELOPMENT CORPORATION (TW) 2010-06-10 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 (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-20100145098-A1 PROCESS FOR PRODUCING CARBOXYLIC ACID ANHYDRIDES CA4, CA9, CA7 SMN1; SMN2 2703/4885KDM4E 947/4885ALDH1A1 200/4885

“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.