Tiotidine

Tiotidine

SCHEMBL7574356

CN=C(NC#N)NCCSCc1csc(N=C(N)N)n1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH2 P25021 4/20 1.00
CYP3A4 P08684 3/20 1.00
CYP2D6 P10635 3/20 1.00
MAPT P10636 1/20 1.00
LMNA P02545 4/20 0.49
TSHR P16473 4/20 0.49
SLC22A2 O15244 3/20 0.49
SLC47A2 Q86VL8 3/20 0.49
SLC47A1 Q96FL8 3/20 0.49
MEN1 O00255 1/20 0.49
CYP1A2 P05177 1/20 0.49
GLA P06280 1/20 0.49
ATP4A P20648 1/20 0.49
APEX1 P27695 1/20 0.49
PDE4A P27815 1/20 0.49
CYP2C19 P33261 1/20 0.49
ADRA1A P35348 1/20 0.49
ATP4B P51164 1/20 0.49
KMT2A Q03164 1/20 0.49
SMN1; SMN2 Q16637 1/20 0.49

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
SCHEMBL10367343 0.87 HRH2 (0.77) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11360309 0.85 CYP3A4 (0.74) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11357836 0.84 CYP3A4 (0.72) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11357832 0.84 CYP3A4 (0.72) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11373962 0.84 CYP3A4 (0.72) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11364135 0.84 CYP3A4 (0.72) HRH2CYP3A4CYP2D6MAPTLMNA
Tiotidine SCHEMBL118501 0.83 HRH2 (0.71) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL29388919 0.83 CYP2D6 (0.71) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11353503 0.83 CYP3A4 (0.70) HRH2CYP3A4CYP2D6MAPTLMNA
SCHEMBL11353499 0.83 CYP3A4 (0.70) HRH2CYP3A4CYP2D6MAPTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250388529-A1 N-Substituted Phenylalkylamines and Their Use as Therapeutic Agents ALEXANDER SHULGIN RES INSTITUTE INC (US) 2025-12-25 US disclosed
US-12415790-B2 GluN2B-subunit selective antagonists of the N-methyl-D-aspartate receptors with enhanced potency at acidic pH EMORY UNIVERSITY (US) 2025-09-16 US disclosed
WO-2025137730-A1 N-SUBSTITUTED TRYPTAMINES AND N-SUBSTITUTED LYSERGAMIDES AND THEIR USE AS THERAPEUTIC AGENTS ALEXANDER SHULGIN RESEARCH INSTITUTE, INC. (US) 2025-06-26 WO disclosed
EP-4543833-A1 N-SUBSTITUTED PHENYLALKYLAMINES AND THEIR USE AS THERAPEUTIC AGENTS Alexander Shulgin Research Institute, Inc. (US) 2025-04-30 EP disclosed
US-20240400528-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH NEUROP, INC. 2024-12-05 US disclosed
US-20240360091-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH NEUROP, INC. 2024-10-31 US disclosed
EP-4395783-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH Emory University (US) 2024-07-10 EP disclosed
WO-2024006226-A1 N-SUBSTITUTED PHENYLALKYLAMINES AND THEIR USE AS THERAPEUTIC AGENTS ALEXANDER SHULGIN RESEARCH INSTITUTE, INC. (US) 2024-01-04 WO disclosed
US-20230349922-A1 H2 Blockers Targeting Liver Macrophages for the Prevention and Treatment of Liver Disease and Cancer UNIVERSITÉ DE STRASBOURG (FR) 2023-11-02 US disclosed
EP-4196793-A1 H2 BLOCKERS TARGETING LIVER MACROPHAGES FOR THE PREVENTION AND TREATMENT OF LIVER DISEASE AND CANCER Université de Strasbourg (FR) 2023-06-21 EP disclosed
WO-2023034589-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH EMORY UNIVERSITY (US) 2023-03-09 WO disclosed
WO-2022034121-A1 H2 BLOCKERS TARGETING LIVER MACROPHAGES FOR THE PREVENTION AND TREATMENT OF LIVER DISEASE AND CANCER UNIVERSITÉ DE STRASBOURG (FR) 2022-02-17 WO disclosed
EP-2576778-B1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN RODENTS UNIV KYOTO (JP) 2017-08-09 EP disclosed
US-9273364-B2 Transgenic reporter system that reveals expression profiles and regulation mechanisms of alternative splicing in mammalian organisms KYOTO UNIVERSITY (JP) 2016-03-01 US disclosed
US-20130137099-A1 TRANSGENIC REPORTER SYSTEM THAT REVEALS EXPRESSION PROFILES AND REGULATION MECHANISMS OF ALTERNATIVE SPLICING IN MAMMALIAN ORGANISMS KYOTO UNIVERSITY (JP) 2013-05-30 US disclosed
EP-1239280-A2 ElogDoct:A tool for lipophilicity determination in drug discovery basic and neutral compounds Pfizer Products Inc. (US) 2002-09-11 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 (4 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-12415790-B2 GluN2B-subunit selective antagonists of the N-methyl-D-aspartate receptors with enhanced potency at acidic pH GRIN2B, GRIN2C, GRIN2A HRH2 559/4885CYP3A4 2252/4885CYP2D6 1450/4885
US-20250388529-A1 N-Substituted Phenylalkylamines and Their Use as Therapeutic Agents CNR2, CNR1, HCN3 HRH2 124/4885CYP3A4 994/4885CYP2D6 630/4885
US-20240400528-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH GRIN2B, GRIN2C, GRIN2A HRH2 473/4885CYP3A4 2251/4885CYP2D6 1620/4885
US-20240360091-A1 GLUN2B-SUBUNIT SELECTIVE ANTAGONISTS OF THE N-METHYL-D-ASPARTATE RECEPTORS WITH ENHANCED POTENCY AT ACIDIC PH GRIN2B, GRIN2C, GRIN2A HRH2 473/4885CYP3A4 2251/4885CYP2D6 1620/4885

“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.