SCHEMBL250620

SCHEMBL250620

O=C(NCO)OCc1ccccc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.67
SMN1; SMN2 Q16637 1/20 0.67
HTT P42858 1/20 0.63
ALDH1A1 P00352 3/20 0.56
CA12 O43570 2/20 0.56
CA1 P00915 2/20 0.56
CA2 P00918 2/20 0.56
CA9 Q16790 2/20 0.56
TGM2 P21980 1/20 0.55
CTSL P07711 1/20 0.55
CTSB P07858 1/20 0.55
CTSS P25774 1/20 0.55
CTSK P43235 1/20 0.55
NPC1 O15118 1/20 0.54
RAB9A P51151 1/20 0.54
POLB P06746 1/20 0.54
L3MBTL1 Q9Y468 1/20 0.54
PLAU P00749 1/20 0.54
KEAP1 Q14145 1/20 0.54
NFE2L2 Q16236 1/20 0.54

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
SCHEMBL31550495 0.90 ALDH1A1 (0.62) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL6741072 0.87 LMNA (0.65) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL11783251 0.87 HTT (0.66) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL126974 0.87 HTT (0.66) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL13055383 0.86 LMNA (0.80) LMNASMN1; SMN2HTTALDH1A1CA12
Hydrochloric Acid SCHEMBL8688569 0.85 HTT (0.64) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL375858 0.85 LMNA (0.73) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL11143560 0.85 LMNA (0.63) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL10081124 0.85 LMNA (0.63) LMNASMN1; SMN2HTTALDH1A1CA12
SCHEMBL8197237 0.85 LMNA (0.67) LMNASMN1; SMN2HTTALDH1A1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260109665-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS INC (US) 2026-04-23 US disclosed
US-20250042843-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS INC (US) 2025-02-06 US disclosed
US-20230122651-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS INC (US) 2023-04-20 US disclosed
US-20220105194-A1 CONJUGATE COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE ASTELLAS PHARMA INC. (JP) 2022-04-07 US disclosed
US-20210340276-A1 COMPLEX HAVING ANTI-HUMAN MUC1 ANTIBODY FAB FRAGMENT, PEPTIDE LINKER AND/OR LIGAND ASTELLAS PHARMA INC. (JP) 2021-11-04 US disclosed
US-20210122709-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS INC (US) 2021-04-29 US disclosed
US-20200055813-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS, INC. 2020-02-20 US disclosed
US-20190077803-A1 TETRACYCLINE COMPOUNDS TETRAPHASE PHARMACEUTICALS INC (US) 2019-03-14 US disclosed
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. 2019-02-07 US disclosed
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA PARATEK PHARMACEUTICALS, INC. 2019-02-07 US disclosed
US-20030166585-A1 Substituted tetracycline compounds as synergistic antifungal agents PARATEK PHARMACEUTICALS, INC. 2003-09-04 US disclosed
US-20030100017-A1 Substituted tetracycline compounds as antifungal agents PARATEK PHARMACEUTICALS, INC. 2003-05-29 US disclosed
WO-2003005971-A2 TETRACYCLINE COMPOUNDS HAVING TARGET THERAPEUTIC ACTIVITIES PARATEK PHARMACEUTICALS, INC. (US) 2003-01-23 WO disclosed
WO-2002085303-A2 SUBSTITUTED TETRACYCLINE COMPOUNDS FOR THE TREATMENT OF MALARIA PARATEK PHARMACEUTICALS, INC. (US) 2002-10-31 WO disclosed
WO-2002072031-A2 SUBSTITUTED TETRACYCLINE COMPOUNDS AS SYNERGISTIC ANTIFUNGAL AGENTS PARATEK PHARMACEUTICALS, INC. (US) 2002-09-19 WO disclosed
WO-2002072022-A2 SUBSTITUTED TETRACYCLINE COMPOUNDS AS ANTIFUNGAL AGENTS PARATEK PHARMACEUTICALS, INC. (US) 2002-09-19 WO disclosed
US-20010038854-A1 Sustained-release preparation TAKEDA PHARMACEUTICAL COMPANY, LIMITED (JP) 2001-11-08 US disclosed
US-6264970-B1 BIODEGRADABLE POLYMER TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2001-07-24 US disclosed
EP-0815853-A2 Sustained-release preparation for bioactive substance having an acidic group TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1998-01-07 EP disclosed
US-4038306-A N-T-BUTOXYCARBONYL-S-LOWER ALKANOYLAMIDOMETHYL-CYSTEINE AND P-NITROPHENYL ESTERS MERCK & CO., INC. (US) 1977-07-26 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 (11 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-20220105194-A1 CONJUGATE COMPRISING LIGAND, SPACER, PEPTIDE LINKER, AND BIOMOLECULE MUC1, CA14, CA13 LMNA 2337/4885SMN1; SMN2 4476/4885HTT 3269/4885
US-20030166585-A1 Substituted tetracycline compounds as synergistic antifungal agents TUBB6, ETF1, TUBB2A LMNA 3309/4885SMN1; SMN2 1859/4885HTT 3268/4885
US-20210340276-A1 COMPLEX HAVING ANTI-HUMAN MUC1 ANTIBODY FAB FRAGMENT, PEPTIDE LINKER AND/OR LIGAND MUC1, SIGLEC7, CA14 LMNA 2413/4885SMN1; SMN2 4502/4885HTT 2215/4885
US-20200055813-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS F7, TUBA1C, TUBA4A LMNA 2405/4885SMN1; SMN2 2831/4885HTT 1112/4885
US-20190040001-A1 METHODS OF USING SUBSTITUTED TETRACYCLINE COMPOUNDS TO MODULATE RNA NSUN3, NSUN2, RNMT LMNA 2369/4885SMN1; SMN2 1627/4885HTT 620/4885
US-20250042843-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS F7, TUBA1C, TUBA4A LMNA 2405/4885SMN1; SMN2 2831/4885HTT 1112/4885
US-20260109665-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS CBR1, CYP7A1, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16 LMNA 2150/4885SMN1; SMN2 2065/4885HTT 1189/4885
US-20010038854-A1 Sustained-release preparation BMP2, PGF, AREG LMNA 1563/4885SMN1; SMN2 1666/4885HTT 4358/4885
US-20230122651-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS F7, TUBA1C, TUBA4A LMNA 2405/4885SMN1; SMN2 2831/4885HTT 1112/4885
US-20190077803-A1 TETRACYCLINE COMPOUNDS TUBB, TUBA1C, TUBA1A LMNA 3089/4885SMN1; SMN2 3203/4885HTT 707/4885
US-20210122709-A1 C7-FLUORO SUBSTITUTED TETRACYCLINE COMPOUNDS F7, TUBA1C, TUBA4A LMNA 2405/4885SMN1; SMN2 2831/4885HTT 1112/4885

“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.