SCHEMBL2679101

SCHEMBL2679101

O=C(Nc1ccc2c(O)cc(S(=O)(=O)O)cc2c1)Nc1ccc2c(O)cc(S(=O)(=O)O)cc2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
PRMT1 Q99873 2/20 1.00
SIRT1 Q96EB6 1/20 0.74
CASP6 P55212 3/20 0.67
CTDSP1 Q9GZU7 1/20 0.67
NT5E P21589 2/20 0.63
NSD2 O96028 2/20 0.60
DUSP3 P51452 2/20 0.60
PTPN5 P54829 2/20 0.60
PTPN11 Q06124 2/20 0.60
CASP7 P55210 1/20 0.52
ENPP2 Q13822 2/20 0.50
CD40 P25942 1/20 0.48
CD40LG P29965 1/20 0.48
CA2 P00918 1/20 0.48
TIMP3 P35625 1/20 0.47

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
SCHEMBL29349608 1.00 PRMT1 (1.00) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL6079067 1.00 PRMT1 (1.00) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL18134576 0.92 PRMT1 (0.84) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL10014033 0.92 PRMT1 (0.84) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL8416221 0.91 PRMT1 (0.83) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL11342001 0.91 PRMT1 (0.82) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL29384348 0.89 PRMT1 (0.81) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL10900036 0.89 PRMT1 (0.81) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL6078935 0.88 PRMT1 (0.78) PRMT1SIRT1CASP6CTDSP1NT5E
SCHEMBL22488772 0.88 PRMT1 (0.78) PRMT1SIRT1CASP6CTDSP1NT5E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4591604-A Method of inhibiting the complement system by administering multisulfonated naphthalene ureas AMERICAN CYANAMID COMPANY (US) 1986-05-27 US claimed
US-20230382945-A1 THERAPEUTIC AGENTS AND METHODS POP TEST ONCOLOGY LLC (US) 2023-11-30 US disclosed
US-20230382945-A1 THERAPEUTIC AGENTS AND METHODS POP TEST ONCOLOGY LLC (US) 2023-11-30 US disclosed
US-11702443-B2 Therapeutic agents and methods POP TEST ONCOLOGY LLC (US) 2023-07-18 US disclosed
US-11702443-B2 Therapeutic agents and methods POP TEST ONCOLOGY LLC (US) 2023-07-18 US disclosed
US-20220168329-A1 COMBINATORIAL DRUG TREATMENT OF CANCER UNIVERSITY OF VIRGINIA 2022-06-02 US disclosed
US-11224599-B2 Therapeutic agents and methods POP TEST ONCOLOGY LLC 2022-01-18 US disclosed
US-20210353623-A1 THERAPEUTIC AGENTS AND METHODS POP TEST ONCOLOGY LLC 2021-11-18 US disclosed
US-11040037-B2 Therapeutic agents and methods POP TEST ONCOLOGY LLC 2021-06-22 US disclosed
US-20190054070-A1 Methods and Compositions for Regenerative Synaptogenesis NEUROTROPE BIOSCIENCE, INC. 2019-02-21 US disclosed
US-6458998-B1 NAPHTHALENEUREAS AS ANTIDIABETIC AGENTS TELIK, INC. 2002-10-01 US disclosed
US-6120561-A Process for the preparation of low-salt, liquid dyestuff preparations BAYER AKTIENGESELLSCHAFT (DE) 2000-09-19 US disclosed
US-5697985-A PREPARING AQUEOUS SLURRY OF ALKALI METAL SALT OF AZO DIRECT DYE, ADDING VISCOSITY ENHANCING AGENT BAYER CORPORATION (US) 1997-12-16 US disclosed
EP-0747450-A2 Process for the preparation of storage-stable dye dispersions Bayer Corporation (US) 1996-12-11 EP disclosed
EP-0235524-B1 PROCESS FOR THE PREPARATION OF CONCENTRATED SOLUTIONS OF ANIONIC DYES BAYER AG (DE) 1992-04-15 EP disclosed
US-4933436-A Process for the preparation of stable aqueous solutions of anionic dyestuffs by conducting diazotization in the presence of an aromatic sulphonic acid BAYER AKTIENGESELLSCHAFT (DE) 1990-06-12 US disclosed
US-4599203-A Multisulfonated naphthalene ureas useful as complement inhibitors AMERICAN CYANAMID COMPANY (US) 1986-07-08 US disclosed
US-4591604-A Method of inhibiting the complement system by administering multisulfonated naphthalene ureas AMERICAN CYANAMID COMPANY (US) 1986-05-27 US disclosed
US-4163012-A DIAZOTIZATION IN THE PRESENCE OF CALCIUM HYDROXIDE BAYER AKTIENGESELLSCHAFT (DE) 1979-07-31 US disclosed
US-4118182-A Solutions of azo dyes derived from 4-4-diamino-2,2-stilbenedisulfonic acid E. I. DU PONT DE NEMOURS AND COMPANY (US) 1978-10-03 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 (7 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-20220168329-A1 COMBINATORIAL DRUG TREATMENT OF CANCER DDIT3, PRMT3, PRMT1 PRMT1 3/4885SIRT1 1279/4885CASP6 1575/4885
US-11702443-B2 Therapeutic agents and methods NR1H4, NR3C1, NR3C2 PRMT1 3314/4885SIRT1 2521/4885CASP6 2608/4885
US-20230382945-A1 THERAPEUTIC AGENTS AND METHODS NR1H4, NR3C1, NR3C2 PRMT1 3314/4885SIRT1 2521/4885CASP6 2608/4885
US-11224599-B2 Therapeutic agents and methods NR1H4, NR3C1, NR3C2 PRMT1 3314/4885SIRT1 2521/4885CASP6 2608/4885
US-20210353623-A1 THERAPEUTIC AGENTS AND METHODS NR1H4, NR3C1, NR3C2 PRMT1 3314/4885SIRT1 2521/4885CASP6 2608/4885
US-20190054070-A1 Methods and Compositions for Regenerative Synaptogenesis PRMT7, DCX, EZH2 PRMT1 4/4885SIRT1 481/4885CASP6 3580/4885
US-11040037-B2 Therapeutic agents and methods NR1H4, NR3C1, NR3C2 PRMT1 3314/4885SIRT1 2521/4885CASP6 2608/4885

“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.