Stilbamidine

Stilbamidine

SCHEMBL871695

N=C(N)c1ccc(/C=C/c2ccc(C(=N)N)cc2)cc1.[Cl-].[Cl-].[H+].[H+]

nearest known ligand 0.91

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

The experimentally established mechanism targets of Stilbamidine. 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
PRMT1 Q99873 3/20 0.91
PRMT5 O14744 1/20 0.91
ALDH1A1 P00352 1/20 0.91
HPGD P15428 1/20 0.91
CYP2C19 P33261 1/20 0.91
HSD17B10 Q99714 1/20 0.91
PLAU P00749 4/20 0.55
PLG P00747 1/20 0.55
PLAT P00750 1/20 0.55
KLK1 P06870 1/20 0.55
LMNA P02545 2/20 0.52
MASP2 O00187 1/20 0.52
THPO P40225 1/20 0.52
F2 P00734 7/20 0.50
PRSS1 P07477 2/20 0.50
PRSS3 P35030 2/20 0.50
APEX1 P27695 1/20 0.50
F10 P00742 6/20 0.48
ST14 Q9Y5Y6 1/20 0.48
F12 P00748 1/20 0.48

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
Stilbamidine SCHEMBL889782 0.95 PRMT1 (1.00) PRMT1PRMT5ALDH1A1HPGDCYP2C19
Stilbamidine SCHEMBL208655 0.95 PRMT1 (1.00) PRMT1PRMT5ALDH1A1HPGDCYP2C19
Stilbamidine SCHEMBL3932459 0.93 PRMT1 (0.95) PRMT1PRMT5ALDH1A1HPGDCYP2C19
SCHEMBL428473 0.86 PRMT1 (0.83) PRMT1PRMT5ALDH1A1HPGDCYP2C19
SCHEMBL428474 0.86 PRMT1 (0.83) PRMT1PRMT5ALDH1A1HPGDCYP2C19
Hydrochloric Acid SCHEMBL11333164 0.85 PRMT1 (0.79) PRMT1PRMT5ALDH1A1HPGDCYP2C19
Hydrochloric Acid SCHEMBL11333159 0.85 PRMT1 (0.79) PRMT1PRMT5ALDH1A1HPGDCYP2C19
SCHEMBL2521983 0.85 PRMT1 (0.79) PRMT1PRMT5ALDH1A1HPGDCYP2C19
SCHEMBL23902148 0.83 PRMT1 (0.76) PRMT1PRMT5ALDH1A1HPGDCYP2C19
SCHEMBL2520059 0.81 ALDH1A1 (0.73) PRMT1PRMT5ALDH1A1HPGDCYP2C19

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
EP-2376074-B1 METHOD FOR IMPROVED BIOACTIVATION OF MEDICATIONS DRITTE PATENTPORTFOLIO BETEILI (DE) 2019-03-13 EP disclosed
US-20120077876-A1 Method For Improved Bioactivation Of Pharmaceuticals DRITTE PATENTPORTFOLIO BETEILIGUNGSGESELLSCHAFT MBH & CO. KG (DE) 2012-03-29 US disclosed
US-7927613-B2 Pharmaceutical co-crystal compositions UNIVERSITY OF SOUTH FLORIDA (US) 2011-04-19 US disclosed
US-7790905-B2 Pharmaceutical propylene glycol solvate compositions MCNEIL-PPC, INC. (US) 2010-09-07 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-20120077876-A1 Method For Improved Bioactivation Of Pharmaceuticals CYP2B6, CYP1A2, CYP2D6 PRMT1 1726/4885PRMT5 2228/4885ALDH1A1 95/4885

“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.