Iodide

Iodide

SCHEMBL492902

CC(C)(C)P(CCP(c1ccccn1)C(C)(C)C)c1ccccn1.CC(C)(C)P(CCP(c1ccccn1)C(C)(C)C)c1ccccn1.[Au+].[I-]

nearest known ligand 0.41

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
KDM4E B2RXH2 6/20 0.41
GAA P10253 1/20 0.41
LMNA P02545 3/20 0.37
CCR1 P32246 2/20 0.37
CCR5 P51681 2/20 0.37
CCR8 P51685 2/20 0.37
CYP1A2 P05177 2/20 0.37
POLB P06746 1/20 0.37
METAP1 P53582 1/20 0.37
BLM P54132 1/20 0.37
HIF1A Q16665 1/20 0.37
DOHH Q9BU89 1/20 0.37
P4HTM Q9NXG6 1/20 0.37
NPC1 O15118 5/20 0.33
RAB9A P51151 5/20 0.33
SMN1; SMN2 Q16637 4/20 0.33
HTT P42858 3/20 0.33
TP53 P04637 3/20 0.32
L3MBTL1 Q9Y468 3/20 0.32
TDP1 Q9NUW8 2/20 0.32

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
Hydrochloric Acid SCHEMBL492457 0.98 KDM4E (0.42) KDM4EGAALMNACCR1CCR5
Hydrochloric Acid SCHEMBL492359 0.98 KDM4E (0.42) KDM4EGAALMNACCR1CCR5
Hydrochloric Acid SCHEMBL492462 0.98 KDM4E (0.42) KDM4EGAALMNACCR1CCR5
Bromide SCHEMBL492578 0.96 KDM4E (0.41) KDM4EGAALMNACCR1CCR5
SCHEMBL492442 0.96 KDM4E (0.44) KDM4EGAALMNACCR1CCR5
Hydrochloric Acid SCHEMBL492668 0.94 KDM4E (0.42) KDM4EGAALMNACCR1CCR5
SCHEMBL4575603 0.94 KDM4E (0.42) KDM4EGAALMNACCR1CCR5
SCHEMBL18406133 0.89 KDM4E (0.41) KDM4EGAALMNACCR1CCR5
SCHEMBL18412682 0.89 KDM4E (0.41) KDM4EGAALMNACCR1CCR5
SCHEMBL9335973 0.84 CYP1A2 (0.41) KDM4EGAALMNACCR1CCR5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1876182-B1 PHOSPHINE TRANSITION METAL COMPLEX, PROCESS FOR PRODUCING THE SAME AND ANTICANCER DRUG CONTAINING THE SAME NIPPON CHEMICAL IND (JP) 2012-12-19 EP claimed
US-8106186-B2 Transition metal phosphine complex, method for producing same, and anticancer agent containing transition metal phospine complex NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2012-01-31 US claimed
US-20090076267-A1 TRANSITION METAL PHOSPHINE COMPLEX, METHOD FOR PRODUCING SAME, AND ANTICANCER AGENT CONTAINING TRANSITION METAL PHOSPINE COMPLEX NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2009-03-19 US claimed
EP-1876182-A1 PHOSPHINE TRANSITION METAL COMPLEX, PROCESS FOR PRODUCING THE SAME AND ANTICANCER DRUG CONTAINING THE SAME Nippon Chemical Industrial Co., Ltd. (JP) 2008-01-09 EP claimed
EP-1876182-B1 PHOSPHINE TRANSITION METAL COMPLEX, PROCESS FOR PRODUCING THE SAME AND ANTICANCER DRUG CONTAINING THE SAME NIPPON CHEMICAL IND (JP) 2012-12-19 EP disclosed
US-8106186-B2 Transition metal phosphine complex, method for producing same, and anticancer agent containing transition metal phospine complex NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2012-01-31 US disclosed
US-20090076267-A1 TRANSITION METAL PHOSPHINE COMPLEX, METHOD FOR PRODUCING SAME, AND ANTICANCER AGENT CONTAINING TRANSITION METAL PHOSPINE COMPLEX NIPPON CHEMICAL INDUSTRIAL CO., LTD. (JP) 2009-03-19 US disclosed
EP-1876182-A1 PHOSPHINE TRANSITION METAL COMPLEX, PROCESS FOR PRODUCING THE SAME AND ANTICANCER DRUG CONTAINING THE SAME Nippon Chemical Industrial Co., Ltd. (JP) 2008-01-09 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 (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-20090076267-A1 TRANSITION METAL PHOSPHINE COMPLEX, METHOD FOR PRODUCING SAME, AND ANTICANCER AGENT CONTAINING TRANSITION METAL PHOSPINE COMPLEX CDKL1, MASTL, AARS1 KDM4E 3657/4885GAA 2569/4885LMNA 4443/4885

“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.