Diphenhydramine

Diphenhydramine

SCHEMBL4193326

CN(C)CCOC(c1ccccc1)c1ccccc1.Cn1c(=O)c2[nH]c(Cl)nc2n(C(=O)O)c1=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

HRH1

The experimentally established mechanism targets of Diphenhydramine. 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
HRH1 known ✓ P35367 4/20 0.81
SMN1; SMN2 Q16637 2/20 1.00
LMNA P02545 6/20 0.81
CHRM2 P08172 5/20 0.81
SLC6A2 P23975 5/20 0.81
SLC6A3 Q01959 5/20 0.81
CYP2D6 P10635 5/20 0.81
ADRA2A P08913 4/20 0.81
CHRM1 P11229 4/20 0.81
ADRA2B P18089 4/20 0.81
CHRM4 P08173 3/20 0.81
CHRM5 P08912 3/20 0.81
CHRM3 P20309 3/20 0.81
HTR2A P28223 3/20 0.81
HTR2C P28335 3/20 0.81
HTR2B P41595 3/20 0.81
CYP1A2 P05177 2/20 0.81
ALDH1A1 P00352 2/20 0.81
ADRA1D P25100 1/20 0.81
HSD17B10 Q99714 1/20 0.81

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
Diphenhydramine SCHEMBL1896940 0.90 LMNA (1.00) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL5128 0.90 LMNA (1.00) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL5670807 0.90 LMNA (1.00) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL5085363 0.89 ALDH1A1 (0.91) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL10385770 0.89 LMNA (0.98) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL7933565 0.89 LMNA (0.98) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL19259450 0.88 LMNA (0.88) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL8575800 0.88 ALDH1A1 (0.88) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL28213087 0.87 LMNA (0.94) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3
Diphenhydramine SCHEMBL8846483 0.86 LMNA (0.89) SMN1; SMN2LMNACHRM2SLC6A2SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8703823-B2 Methods for treatment of migraine and symptoms thereof SALEHANI FOAD (US) 2014-04-22 US disclosed
US-20090018205-A1 METHODS FOR TREATMENT OF MIGRAINE AND SYMPTOMS THEREOF SALEHANI FOAD 2009-01-15 US disclosed
US-20050282879-A1 Methods and composition for treatment of migraine and symptoms thereof SALEHANI FOAD 2005-12-22 US disclosed
EP-0817618-A1 SOFT GELATIN CAPSULE WITH A GELATIN SHELL COMPRISING XANTHINE DERIVATIVE THE PROCTER & GAMBLE COMPANY (US) 1998-01-14 EP disclosed
US-5641512-A SHELL CONTAINS XANTHINE DERIVATIVE THE PROCTER & GAMBLE COMPANY (US) 1997-06-24 US disclosed
EP-0741560-A1 PROCESS FOR SOLUBILIZING DIFFICULTLY SOLUBLE PHARMACEUTICAL ACTIVES THE PROCTER & GAMBLE COMPANY (US) 1996-11-13 EP disclosed
WO-1996029997-A1 SOFT GELATIN CAPSULE WITH A GELATIN SHELL COMPRISING XANTHINE DERIVATIVE THE PROCTER & GAMBLE COMPANY (US) 1996-10-03 WO disclosed
US-5510389-A CONTAINING ACETAMINOPHEN FORMED BY ADDING AN ELECTROPHILIC BECKMAN REARRANGEMENT CATALYST TO 4-HYDROXYACETOPHENONE OXIME, A POLYOXYETHYLENE GLYCOL, POLYVINYLPYRROLIDONE, AND PROPYLENE GLYCOL; SOLUBILITY, STABILITY THE PROCTER & GAMBLE COMPANY (US) 1996-04-23 US disclosed
US-5484606-A STABILITY THE PROCTER & GAMBLE COMPANY (US) 1996-01-16 US disclosed
WO-1995019759-A1 PROCESS FOR SOLUBILIZING DIFFICULTLY SOLUBLE PHARMACEUTICAL ACTIVES THE PROCTER & GAMBLE COMPANY (US) 1995-07-27 WO disclosed
WO-1995019792-A1 PROCESS FOR REDUCING THE PRECIPITATION OF DIFFICULTLY SOLUBLE PHARMACEUTICAL ACTIVES THE PROCTER & GAMBLE COMPANY (US) 1995-07-27 WO disclosed
EP-0591346-A1 PROCESS FOR SOLUBILIZING DIFFICULTLY SOLUBLE PHARMACEUTICAL ACTIVES RICHARDSON-VICKS, INC. (US) 1994-04-13 EP disclosed
WO-1993000072-A1 PROCESS FOR SOLUBILIZING DIFFICULTLY SOLUBLE PHARMACEUTICAL ACTIVES RICHARDSON VICKS, INC. (US) 1993-01-07 WO 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-20050282879-A1 Methods and composition for treatment of migraine and symptoms thereof HRH3, HRH4, HNMT HRH1 5/4885SMN1; SMN2 2726/4885LMNA 2109/4885
US-20090018205-A1 METHODS FOR TREATMENT OF MIGRAINE AND SYMPTOMS THEREOF HNMT, HRH3, HRH4 HRH1 5/4885SMN1; SMN2 3026/4885LMNA 2521/4885

“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.