SCHEMBL1493181

SCHEMBL1493181

OCC1OC1Cc1ccccc1

nearest known ligand 0.49

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ TSHR P16473 1/20 0.42
▸ SLC5A2 P31639 4/20 0.41
▸ TLR9 Q9NR96 1/20 0.41
▸ GBA1 P04062 1/20 0.39
▸ TDP1 Q9NUW8 1/20 0.39
▸ PDE4D Q08499 1/20 0.39
▸ SLC6A2 P23975 1/20 0.38
▸ SLC6A4 P31645 1/20 0.38
▸ SLC6A3 Q01959 1/20 0.38
▸ CTRB1 P17538 1/20 0.38
▸ HPGD P15428 1/20 0.38

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
SCHEMBL5195874 1.00 TSHR (0.42) TSHRSLC5A2TLR9GBA1TDP1
SCHEMBL8310780 1.00 TSHR (0.42) TSHRSLC5A2TLR9GBA1TDP1
SCHEMBL5195871 1.00 TSHR (0.42) TSHRSLC5A2TLR9GBA1TDP1
SCHEMBL31231840 0.89 TLR9 (0.47) TSHRTLR9GBA1SLC6A2SLC6A4
SCHEMBL12459457 0.86 SLC5A2 (0.53) SLC5A2
SCHEMBL12582923 0.86 SLC5A2 (0.53) SLC5A2
SCHEMBL7147747 0.86 SLC5A2 (0.53) SLC5A2
SCHEMBL13446904 0.84 SLC5A2 (0.55) SLC5A2
SCHEMBL7173273 0.83 TLR9 (0.42) TSHRSLC5A2TLR9GBA1TDP1
SCHEMBL12582958 0.80 SLC5A2 (0.44) SLC5A2

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 54 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0987595-B1 Method of making hydroxy-substituted hydroxylamines and color developers containing same EASTMAN KODAK CO (US) 2004-06-16 — — EP claimed
EP-0987595-A1 Method of making hydroxy-substituted hydroxylamines and color developers containing same EASTMAN KODAK COMPANY (US) 2000-03-22 — — EP claimed
US-6028225-A REACTING HYDROXYLAMINE OR A MONO-SUBSTITUTED HYDROXYLAMINE, IN FREE BASE FORM, WITH AN EPOXIDE; CAN BE USED WITHOUT ISOLATION FROM THE REACTION SOLUTION, COMBINED WITH A COLOR DEVELOPING AGENT; ODORLESS, BY-PRODUCT INHIBITION EASTMAN KODAK COMPANY (US) 2000-02-22 — — US claimed
US-5709982-A MIXTURE OF A HYDROXYLAMINE AND EPOXIDE EASTMAN KODAK COMPANY (US) 1998-01-20 — — US claimed
US-5620835-A MIXTURE OF AN HYDROXYLAMINE AND EPOXIDE EASTMAN KODAK COMPANY (US) 1997-04-15 — — US claimed
US-5508155-A WATER SOLUBLE EASTMAN KODAK COMPANY (US) 1996-04-16 — — US claimed
US-9889115-B2 Fitness assay and associated methods BOARD OF TRUSTEES OF THE UNIVERSITY OF ILLINOIS (US) 2018-02-13 — — US disclosed
EP-2336134-B1 Fitness assay and methods for reducing resistance of HIV to therapy US OF AMERICA REPRESENTED BY THE SECRETARY DEPT OF HEALTH AND HUMAN SERVICES (US) 2016-08-31 — — EP disclosed
CN-102844385-B The surface treatment of cement matrix WACKER CHEMIE AG (DE) 2016-01-20 — — CN disclosed
US-9233943-B2 Process for synthesis of syn azido epdxide and its use as intermediate for the synthesis of amprenavir and saquinavir COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2016-01-12 — — US disclosed
EP-1088098-B2 FITNESS ASSAY AND METHODS FOR REDUCING RESISTANCE OF HIV TO THERAPY US OF AMERICA REPRESENTED BY THE SECRETARY DEPT OF HEALTH AND HUMAN SERVICES (US) 2015-07-01 — — EP disclosed
US-20150011782-A1 PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE FOR THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR COUNCIL OF SCIENTIFIC & INDUSTRIAL RESEARCH (IN) 2015-01-08 — — US disclosed
US-20140011815-A1 FITNESS ASSAY AND ASSOCIATED METHODS THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY, DEPARTMENT OF HEALTH AND HUMAN SERVICES 2014-01-09 — — US disclosed
WO-1997042180-A1 PROCESS FOR PREPARING OXIRANEMETHANAMINE DERIVATIVES BOEHRINGER INGELHEIM PHARMACEUTICALS, INC. (US) 1997-11-13 — — WO disclosed
US-5620835-A MIXTURE OF AN HYDROXYLAMINE AND EPOXIDE EASTMAN KODAK COMPANY (US) 1997-04-15 — — US disclosed
US-5508155-A WATER SOLUBLE EASTMAN KODAK COMPANY (US) 1996-04-16 — — US disclosed
US-5277895-A Nuclear magnetic resonance SCHERING AKTIENGESELLSCHAFT (DE) 1994-01-11 — — US disclosed
EP-0485045-A2 Mono-N-substituted 1,4,7,10-Tetraazacyclododecan-derivatives, process for their preparation and pharmaceutical agent containing them SCHERING AKTIENGESELLSCHAFT (DE) 1992-05-13 — — EP disclosed
US-5084582-A Ruthenium catalyst for oxidation of alcohols to acids SOCIETE NATIONALE ELF AQUITAINE (FR) 1992-01-28 — — US disclosed
EP-0362628-A2 6-Membered lactones and process for their production Takano, Seiichi (JP) 1990-04-11 — — 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 (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-20140011815-A1 FITNESS ASSAY AND ASSOCIATED METHODS CPS1, CTSS, TST TSHR 3041/4885SLC5A2 2171/4885TLR9 4208/4885
US-20150011782-A1 PROCESS FOR SYNTHESIS OF SYN AZIDO EPOXIDE AND ITS USE AS INTERMEDIATE FOR THE SYNTHESIS OF AMPRENAVIR & SAQUINAVIR POR, CYP3A4, CYP2S1 TSHR 3483/4885SLC5A2 3749/4885TLR9 3588/4885

“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.

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