SCHEMBL18725593

SCHEMBL18725593

O=C([O-])c1ccc(N=Nc2ccc(C(=O)[O-])cc2)cc1.[Na+].[Na+]

nearest known ligand 0.58

Known targets — ChEMBL curated mechanism

ABCC8ACEADORA1ADORA2AADORA2BADORA3ALDH5A1ALOX5ALOX5APATP4AATP4BBRAFCA1CA12CA2CA4CYSLTR1DHFRDPEP1EDNRAEDNRBESR2F10FDPSFGF1GABBR1GABBR2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQGARTGNRHRGSC1HMGCRIMPDH1IMPDH2KCNJ11LY96NOD2NR3C1NS3NS4ANS5bP2RY1P2RY12P2RY2P2RY4P2RY6PBP2XPDE3APDE3BPDE4APDE4BPDE4CPDE4DPDK1PDK2PDK3PDK4PPARGPPATPTGIRPTGS1PTGS2RAF1RYR1RYR3SCN10ASCN11ASCN1ASCN2ASCN3ASCN4ASCN5ASCN7ASCN8ASCN9ASERPINC1SLC12A1SLC12A3SYKTHRATHRBTLR3TLR4TLR9TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8TYMSVKORC1XDHblablaIMP-1blaOXA-33blaOXA-58blaT-3blaT-4blaT-5blaT-6dacAdacBdacCfolAfolPfolP1ftsIfusAgaggyrAgyrBmecAmrcAmrcBmrdApbp1apbp1bpbp2pbp2apbp2bpbp3pbp4pbpApbpBpbpCpbpFpolponBrplArplBrplCrplDrplErplFrplJrplKrplLrplMrplNrplOrplPrplQrplRrplSrplTrplUrplVrplWrplXrplYrpmArpmBrpmCrpmDrpmErpmFrpmGrpmHrpmIrpmJrpoArpoBrpoCrpoZrpsArpsBrpsCrpsDrpsErpsFrpsGrpsHrpsIrpsJrpsKrpsLrpsMrpsNrpsOrpsPrpsQrpsRrpsSrpsTrpsUykgMykgO

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ CA2 known ✓ P00918 16/20 0.58
▸ CA1 known ✓ P00915 15/20 0.58
▸ CA4 known ✓ P22748 1/20 0.54
▸ MAPT P10636 3/20 0.56
▸ TRPA1 O75762 1/20 0.52
▸ NPC1 O15118 2/20 0.48
▸ RAB9A P51151 2/20 0.48
▸ MAPK1 P28482 1/20 0.48
▸ STAT3 P40763 1/20 0.48
▸ STAT1 P42224 1/20 0.48
▸ SMN1; SMN2 Q16637 1/20 0.48
▸ TDP1 Q9NUW8 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
SCHEMBL18725592 1.00 CA2 (0.58) CA2CA1MAPTCA4TRPA1
SCHEMBL28820952 0.95 MAPT (0.56) CA2CA1MAPTCA4TRPA1
Potassium Ion SCHEMBL766299 0.95 MAPT (0.61) CA2CA1MAPTCA4TRPA1
Potassium Ion SCHEMBL766298 0.95 MAPT (0.61) CA2CA1MAPTCA4TRPA1
SCHEMBL28556565 0.91 TRPA1 (0.67) CA2CA1MAPTCA4TRPA1
SCHEMBL11268165 0.84 NPC1 (0.69) CA2CA1MAPTNPC1RAB9A
SCHEMBL11862685 0.84 NPC1 (0.69) CA2CA1MAPTNPC1RAB9A
Terephthalic Acid SCHEMBL104073 0.84 CA2 (0.78) CA2CA1MAPTCA4
Terephthalic Acid SCHEMBL31095056 0.84 CA2 (0.78) CA2CA1MAPTCA4
SCHEMBL28143286 0.83 CA2 (0.56) CA2CA1MAPTCA4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111696792-A Organic nanometer negative electrode based on insertion layer type pseudo-capacitor and preparation method and application thereof 苏州大学 2020-09-22 — — CN claimed
CN-117285689-B Self-repairing type light-response polyurea material and preparation method thereof 西南石油大学 2024-02-02 — — CN disclosed
CN-117285689-A Self-repairing type light-response polyurea material and preparation method thereof 西南石油大学 2023-12-26 — — CN disclosed
CN-111696792-B Organic nanometer negative electrode based on insertion layer type pseudo-capacitor and preparation method and application thereof 苏州大学 2021-07-20 — — CN disclosed
CN-108273478-B Formaldehyde removal composition and product 李怀玉 2021-03-02 — — CN disclosed
CN-111696792-A Organic nanometer negative electrode based on insertion layer type pseudo-capacitor and preparation method and application thereof 苏州大学 2020-09-22 — — CN disclosed
US-10159642-B2 Functional polymer gel containing organic nanotubes and method for producing same SEED CO., LTD. (JP) 2018-12-25 — — US disclosed
US-20170112761-A1 FUNCTIONAL POLYMER GEL CONTAINING ORGANIC NANOTUBES AND METHOD FOR PRODUCING SAME SEED CO., LTD. (JP) 2017-04-27 — — US disclosed
EP-3156076-A1 FUNCTIONAL POLYMER GEL CONTAINING ORGANIC NANOTUBES AND METHOD FOR PRODUCING SAME Seed Co., Ltd. (JP) 2017-04-19 — — 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-10159642-B2 Functional polymer gel containing organic nanotubes and method for producing same TAGLN2, ILK, TLN1 CA2 2901/4885CA1 3263/4885CA4 3190/4885
US-20170112761-A1 FUNCTIONAL POLYMER GEL CONTAINING ORGANIC NANOTUBES AND METHOD FOR PRODUCING SAME TAGLN2, ILK, TLN1 CA2 2901/4885CA1 3263/4885CA4 3190/4885

“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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