SCHEMBL1012163

SCHEMBL1012163

Nc1cccc2c(Cl)c[nH]c12

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ IMPDH2 P12268 1/20 0.50
▸ NR4A2 P43354 1/20 0.48
▸ CA12 O43570 2/20 0.45
▸ CA1 P00915 2/20 0.45
▸ CA2 P00918 2/20 0.45
▸ CA3 P07451 1/20 0.45
▸ CA6 P23280 1/20 0.45
▸ CA5A P35218 1/20 0.45
▸ CA7 P43166 1/20 0.45
▸ CA9 Q16790 1/20 0.45
▸ CRBN Q96SW2 1/20 0.45
▸ CA14 Q9ULX7 1/20 0.45
▸ CA5B Q9Y2D0 1/20 0.45
▸ HTR2A P28223 1/20 0.43
▸ TSHR P16473 3/20 0.42
▸ ALDH1A1 P00352 3/20 0.42
▸ TDP1 Q9NUW8 3/20 0.42
▸ CYP3A4 P08684 2/20 0.42
▸ HPGD P15428 2/20 0.42
▸ HSD17B10 Q99714 2/20 0.42

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
SCHEMBL30799504 1.00 IMPDH2 (0.50) IMPDH2NR4A2CA12CA1CA2
Hydrochloric Acid SCHEMBL8834789 0.98 IMPDH2 (0.49) IMPDH2NR4A2CA12CA1CA2
SCHEMBL28251367 0.80 DYRK1A (0.60) NR4A2CA12CA1CA2CA3
SCHEMBL12865280 0.75 TRIM24 (0.55) NR4A2CA12CA1CA2CA3
SCHEMBL30215956 0.75 IMPDH2 (0.50) IMPDH2NR4A2TSHRALDH1A1TDP1
SCHEMBL24743296 0.75 DYRK1A (0.55) NR4A2CA12CA1CA2CA3
SCHEMBL7089054 0.75 REN (0.50) IMPDH2NR4A2HTR2ATSHRALDH1A1
SCHEMBL28002632 0.75 IMPDH2 (0.50) IMPDH2HTR2ATSHRALDH1A1TDP1
SCHEMBL5266825 0.75 IMPDH2 (0.50) IMPDH2NR4A2TSHRALDH1A1TDP1
SCHEMBL13094226 0.72 IMPDH2 (0.51) IMPDH2HTR2ATSHRALDH1A1TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1221533-C Heterobicyclic sulfonamide derivative and sulfonic ester derivative EISAI CO LTD (JP) 2005-10-05 — — CN claimed
US-20260116874-A1 HETEROAROMATIC INDOLESULFONAMIDES SEED THERAPEUTICS INC (US) 2026-04-30 — — US disclosed
EP-4724106-A1 PROTACS AND HYT-PD MOLECULES FOR TARGETED PROTEIN DEGRADATION OF DCAF15 AND THEIR USE IN THE TREATMENT OF AMYLOIDOSIS Kræftens bekæmpelse (DK) 2026-04-15 — — EP disclosed
EP-4704836-A1 HETEROAROMATIC INDOLESULFONAMIDES Seed Therapeutics, Inc (US) 2026-03-11 — — EP disclosed
US-20250368627-A1 PYRAZOLESULFONAMIDES AS ANTITUMOR AGENTS Peloton Therapeutics, Inc., a fully owned subsidiary of Merck Sharp & Dohme LLC (US) 2025-12-04 — — US disclosed
EP-4634155-A1 RBM39 SULFONAMIDE INHIBITORS Recursion Pharmaceuticals, Inc. (US) 2025-10-22 — — EP disclosed
CN-119630658-A Heterocyclic RBM39 modulators 递归医药公司 2025-03-14 — — CN disclosed
WO-2024251876-A1 PROTACs AND HyT-PD MOLECULES FOR TARGETED PROTEIN DEGRADATION OF DCAF15 AND THEIR USE IN THE TREATMENT OF AMYLOIDOSIS KRæFTENS BEKæMPELSE (DK) 2024-12-12 — — WO disclosed
CN-115666575-B Compounds and uses thereof 福宏治疗公司 2024-12-10 — — CN disclosed
US-20240390387-A1 SULFONAMIDE OR SULFINAMIDE COMPOUND HAVING EFFECT OF INDUCING BRD4 PROTEIN DEGRADATION AND PHARMACEUTICAL USE THEREOF MITSUBISHI TANABE PHARMA CORPORATION (JP) 2024-11-28 — — US disclosed
US-6544981-B2 Anticoagulants, cardiovascular disorders BRISTOL-MYERS SQUIBB COMPANY 2003-04-08 — — US disclosed
EP-1294716-A1 LACTAM INHIBITORS OF FACTOR XA AND METHOD Bristol-Myers Squibb Company (US) 2003-03-26 — — EP disclosed
CN-1396833-A Integrin expression inhibitors EISAI CO LTD (JP) 2003-02-12 — — CN disclosed
EP-1258252-A1 INTEGRIN EXPRESSION INHIBITORS Eisai Co., Ltd. (JP) 2002-11-20 — — EP disclosed
WO-2002034744-A1 QUINAZOLINE DERIVATIVES ASTRAZENECA AB (SE) 2002-05-02 — — WO disclosed
US-20020025957-A1 Lactam inhibitors of factor Xa and method BRISTOL-MYERS SQUIBB COMPANY 2002-02-28 — — US disclosed
CN-1079097-C Heterobicyclic sulfonamide derivatives and sulfonate derivatives EISAI CO LTD (JP) 2002-02-13 — — CN disclosed
WO-2001096331-A1 LACTAM INHIBITORS OF FACTOR XA AND METHOD BRISTOL-MYERS SQUIBB COMPANY (US) 2001-12-20 — — WO disclosed
CN-1114506-A Heterobicyclic sulfonamide derivatives and sulfonate derivatives EISAI CO LTD (JP) 1996-01-03 — — CN disclosed
EP-0673937-A1 BICYCLIC HETEROCYCLIC SULFONAMIDE AND SULFONIC ESTER DERIVATIVES Eisai Co., Ltd. (JP) 1995-09-27 — — 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-20260116874-A1 HETEROAROMATIC INDOLESULFONAMIDES DCAF1, DCAF15, DDX39B IMPDH2 2210/4885NR4A2 1356/4885CA12 3806/4885
US-20250368627-A1 PYRAZOLESULFONAMIDES AS ANTITUMOR AGENTS RBM39, RBM3, RBM28 IMPDH2 2527/4885NR4A2 2756/4885CA12 4554/4885
US-20240390387-A1 SULFONAMIDE OR SULFINAMIDE COMPOUND HAVING EFFECT OF INDUCING BRD4 PROTEIN DEGRADATION AND PHARMACEUTICAL USE THEREOF BRD4, BRD1, BRD2 IMPDH2 3263/4885NR4A2 1278/4885CA12 4426/4885
US-20020025957-A1 Lactam inhibitors of factor Xa and method F9, F7, F11 IMPDH2 2809/4885NR4A2 3138/4885CA12 2359/4885

“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.

Send feedback