SCHEMBL2013270

SCHEMBL2013270

O=C(Nc1ccccc1)c1ccc(NC(=O)C2CC[N]CC2)cc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KMT2A Q03164 5/20 0.59
▸ KCNK3 O14649 1/20 0.59
▸ KCNK9 Q9NPC2 1/20 0.59
▸ MEN1 O00255 3/20 0.59
▸ MAPT P10636 2/20 0.59
▸ GAA P10253 1/20 0.59
▸ GFER P55789 1/20 0.59
▸ NPC1 O15118 3/20 0.56
▸ RAB9A P51151 3/20 0.56
▸ HPGD P15428 1/20 0.56
▸ PTPN1 P18031 2/20 0.54
▸ CASP3 P42574 2/20 0.52
▸ SENP7 Q9BQF6 2/20 0.52
▸ SENP8 Q96LD8 1/20 0.52
▸ SENP6 Q9GZR1 1/20 0.52
▸ SIRT5 Q9NXA8 1/20 0.52
▸ KDM4E B2RXH2 2/20 0.51
▸ SIRT1 Q96EB6 1/20 0.51
▸ HDAC2 Q92769 1/20 0.51
▸ HDAC8 Q9BY41 1/20 0.51

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
SCHEMBL8086908 0.89 HPGD (0.69) KMT2AMEN1MAPTGAAGFER
SCHEMBL10306602 0.81 MAPT (0.58) KMT2AKCNK3KCNK9MEN1MAPT
SCHEMBL10055001 0.78 GAA (0.85) KMT2AMEN1MAPTGAAGFER
SCHEMBL29675219 0.78 GAA (0.85) KMT2AMEN1MAPTGAAGFER
SCHEMBL501924 0.78 GAA (0.85) KMT2AMEN1MAPTGAAGFER
SCHEMBL14715847 0.78 PTPN1 (0.84) KMT2AKCNK3KCNK9MEN1MAPT
SCHEMBL4677815 0.77 KMT2A (0.63) KMT2AMEN1MAPTGAAGFER
Hydrochloric Acid SCHEMBL1804763 0.76 GAA (0.82) KMT2AMEN1MAPTGAAGFER
SCHEMBL13552831 0.76 KMT2A (0.65) KMT2ANPC1RAB9ASMN1; SMN2NAMPT
SCHEMBL26953087 0.76 PTPN1 (0.88) KMT2AKCNK3KCNK9MEN1MAPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 — — EP claimed
EP-3268375-B1 PHOTOCHROMIC THIENOCHROMENE COMPOUNDS TRANSITIONS OPTICAL INC (US) 2022-06-15 — — EP claimed
EP-3071576-B9 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-12-22 — — EP claimed
EP-3071576-B1 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-08-18 — — EP claimed
US-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds TRANSITIONS OPTICAL, LTD. (IE) 2020-02-13 — — US claimed
CN-105829283-A Fused ring indeno compounds for preparation of photochromic compounds 光学转变公司 2016-08-03 — — CN claimed
CN-105829319-A Photochromic indeno-fused ring pyran compounds 光学转变公司 2016-08-03 — — CN claimed
EP-2652552-B9 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS TRANSITIONS OPTICAL INC (US) 2016-02-17 — — EP claimed
CN-105143397-A Photochromic articles that include photochromic-dichroic materials TRANSITIONS OPTICAL INC 2015-12-09 — — CN claimed
EP-2652552-B1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS TRANSITIONS OPTICAL INC (US) 2015-09-02 — — EP claimed
US-9051332-B1 Photochromic indeno-fused ring pyran compounds TRANSITIONS OPTICAL, INC. (US) 2015-06-09 — — US claimed
US-20150141661-A1 Photochromic Indeno-Fused Ring Pyran Compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-21 — — US claimed
US-9029565-B1 Fused ring indeno compounds for preparation of photochromic compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-12 — — US claimed
US-8545984-B2 Photochromic compounds and compositions TRANSITIONS OPTICAL, INC. (US) 2013-10-01 — — US claimed
US-20110129678-A1 Photochromic compounds and compositions TRANSITIONS OPTICAL, INC. (US) 2011-06-02 — — US claimed
EP-1639058-A1 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL, INC. (US) 2006-03-29 — — EP claimed
WO-2005005570-A1 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL, INC. (US) 2005-01-20 — — WO claimed
US-20050004361-A1 Thermally reversible; absorption ratio greater than 2.3 TRANSITIONS OPTICAL LIMITED (IE) 2005-01-06 — — US claimed
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 — — EP disclosed
US-20050004361-A1 Thermally reversible; absorption ratio greater than 2.3 TRANSITIONS OPTICAL LIMITED (IE) 2005-01-06 — — 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 (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-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds ALDH1A2, RB1, INCENP KMT2A 1736/4885KCNK3 2654/4885KCNK9 3874/4885
US-20050004361-A1 Thermally reversible; absorption ratio greater than 2.3 CCND1, CCND3, CCND2 KMT2A 1838/4885KCNK3 2287/4885KCNK9 3506/4885
US-20110129678-A1 Photochromic compounds and compositions CRY2, CRY1, PPOX KMT2A 1960/4885KCNK3 2745/4885KCNK9 2278/4885
US-20150141661-A1 Photochromic Indeno-Fused Ring Pyran Compounds INF2, INCENP, RB1 KMT2A 1384/4885KCNK3 1806/4885KCNK9 3459/4885

“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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