SCHEMBL4903616

SCHEMBL4903616

O=C(Cl)c1cc(Cl)c(O)c(Cl)c1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TTR P02766 2/20 0.65
▸ HSD17B10 Q99714 4/20 0.50
▸ TSHR P16473 4/20 0.50
▸ ALDH1A1 P00352 2/20 0.50
▸ CYP3A4 P08684 1/20 0.50
▸ RECQL P46063 1/20 0.50
▸ THRB P10828 1/20 0.46
▸ ESR1 P03372 1/20 0.44
▸ CYP1A2 P05177 1/20 0.44
▸ CYP2C9 P11712 1/20 0.44
▸ ALOX15 P16050 1/20 0.44
▸ ALOX12 P18054 1/20 0.44
▸ CYP2C19 P33261 1/20 0.44
▸ SMN1; SMN2 Q16637 1/20 0.44
▸ HIF1A Q16665 1/20 0.44
▸ AKR1C4 P17516 1/20 0.41
▸ AKR1C3 P42330 1/20 0.41
▸ AKR1C2 P52895 1/20 0.41
▸ AKR1C1 Q04828 1/20 0.41
▸ HPGD P15428 2/20 0.40

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
SCHEMBL10921198 0.86 TTR (0.48) TTRHSD17B10TSHRALDH1A1CYP3A4
SCHEMBL11184770 0.84 TTR (0.48) TTRHSD17B10TSHRALDH1A1CYP3A4
SCHEMBL3422274 0.81 TTR (0.68) TTRHSD17B10TSHRALDH1A1CYP3A4
SCHEMBL983196 0.81 HPGD (0.46) TTRHSD17B10TSHRALDH1A1CYP3A4
SCHEMBL22000624 0.80 TTR (0.44) TTR
SCHEMBL4898203 0.80 MEN1 (0.55) TTRHSD17B10ALDH1A1HPGDSLC22A12
SCHEMBL737305 0.79 TTR (1.00) TTRHSD17B10TSHRALDH1A1CYP3A4
SCHEMBL104060 0.79 ALDH1A1 (0.54) TTRTSHRALDH1A1HPGDMEN1
SCHEMBL4901895 0.78 GPR35 (0.61) TTRTSHRALDH1A1CYP3A4
SCHEMBL4104322 0.77 TTR (0.62) TTRHSD17B10TSHRALDH1A1CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111675675-A Preparation method of dortinode 苏州明锐医药科技有限公司 2020-09-18 — — CN claimed
US-3951914-A Process for preparing poly(1,4-benzamide) in cyclic sulfone media E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-04-20 — — US claimed
CN-119930540-A Multi-tenor preparation method of mine 杭州善礼生物医药科技有限公司 2025-05-06 — — CN disclosed
CN-119504641-A Multi-tenor preparation method of mine 南京唯创远医药科技有限公司 2025-02-25 — — CN disclosed
US-10005750-B2 Developing potent urate transporter inhibitors: compounds designed for their uricosuric action J-PHARMA CO., LTD. (JP) 2018-06-26 — — US disclosed
US-20130225673-A1 DEVELOPING POTENT URATE TRANSPORTER INHIBITORS: COMPOUNDS DESIGNED FOR THEIR URICOSURIC ACTION J-PHARMA CO., LTD. (JP) 2013-08-29 — — US disclosed
WO-2012048058-A2 DEVELOPING POTENT URATE TRANSPORTER INHIBITORS: COMPOUNDS DESIGNED FOR THEIR URICOSURIC ACTION J-PHARMA CO., LTD. (JP) 2012-04-12 — — WO disclosed
US-20080305169-A1 Pharmaceutical Compositions Comprising Nitrogen-Containing Fused Ring Coumpounds JAPAN TOBACCO INC. (JP) 2008-12-11 — — US disclosed
US-20080064871-A1 Production Method of Nitrogen-Containing Fused Ring Compounds JAPAN TOBACCO INC. (JP) 2008-03-13 — — US disclosed
EP-1820515-A1 NITROGEN-CONTAINING FUSED RING COMPOUND AND USE THEREOF Japan Tobacco, Inc. (JP) 2007-08-22 — — EP disclosed
US-20070010670-A1 Nitrogen-containing fused ring compounds and use thereof JAPAN TOBACCO INC. (JP) 2007-01-11 — — US disclosed
US-4400387-A USEFUL IN VETERINARY MEDICINE FOR TREATMENT OF PSYCHOLOGICAL DISORDERS S. A. LABAZ-SANOFI N.V. (FR) 1983-08-23 — — US disclosed
US-3991016-A Poly(1,4-benzamide) copolymers E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-11-09 — — US disclosed
US-3951914-A Process for preparing poly(1,4-benzamide) in cyclic sulfone media E. I. DU PONT DE NEMOURS AND COMPANY (US) 1976-04-20 — — 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 (5 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-10005750-B2 Developing potent urate transporter inhibitors: compounds designed for their uricosuric action SLCO2B1, SLCO2A1, SLC10A6 TTR 1944/4885HSD17B10 419/4885TSHR 655/4885
US-20080305169-A1 Pharmaceutical Compositions Comprising Nitrogen-Containing Fused Ring Coumpounds NOD1, NLRP3, SLC10A1 TTR 2377/4885HSD17B10 313/4885TSHR 4311/4885
US-20070010670-A1 Nitrogen-containing fused ring compounds and use thereof NUDT1, NOD1, SLC28A1 TTR 2758/4885HSD17B10 633/4885TSHR 3246/4885
US-20130225673-A1 DEVELOPING POTENT URATE TRANSPORTER INHIBITORS: COMPOUNDS DESIGNED FOR THEIR URICOSURIC ACTION SLCO2B1, SLCO2A1, SLC10A6 TTR 1944/4885HSD17B10 419/4885TSHR 655/4885
US-20080064871-A1 Production Method of Nitrogen-Containing Fused Ring Compounds NOD1, XDH, URB2 TTR 1857/4885HSD17B10 516/4885TSHR 3482/4885

“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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