SCHEMBL433614

SCHEMBL433614

CCCCCCc1c2nc(c(CCCCCC)c3ccc([nH]3)c(CCCCCC)c3nc(c(CCCCCC)c4ccc1[nH]4)C=C3)C=C2

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ KCNH2 Q12809 1/20 0.42
▸ HSD17B10 Q99714 3/20 0.39
▸ KDM4E B2RXH2 2/20 0.39
▸ ALDH1A1 P00352 2/20 0.39
▸ HPGD P15428 2/20 0.39
▸ TERT O14746 1/20 0.38
▸ CCNB2 O95067 1/20 0.37
▸ CDK1 P06493 1/20 0.37
▸ CCNB1 P14635 1/20 0.37
▸ GSK3A P49840 1/20 0.37
▸ GSK3B P49841 1/20 0.37
▸ CCNB3 Q8WWL7 1/20 0.37
▸ GAA P10253 1/20 0.37
▸ LMNA P02545 1/20 0.37
▸ MAPT P10636 1/20 0.37
▸ XBP1 P17861 1/20 0.37
▸ HTT P42858 1/20 0.37
▸ SMN1; SMN2 Q16637 1/20 0.37
▸ NPSR1 Q6W5P4 1/20 0.37
▸ GPR84 Q9NQS5 5/20 0.37

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
SCHEMBL15468129 1.00 KCNH2 (0.42) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL8601755 1.00 KCNH2 (0.42) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL9438134 1.00 KCNH2 (0.42) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL1194293 0.98 KCNH2 (0.39) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL3475623 0.93 MAPT (0.41) HSD17B10KDM4EALDH1A1HPGDTERT
SCHEMBL17419216 0.91 KCNH2 (0.36) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL6003452 0.91 KCNH2 (0.36) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL6004323 0.90 CCNB2 (0.35) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL7262879 0.89 TERT (0.34) KCNH2HSD17B10KDM4EALDH1A1HPGD
SCHEMBL6003423 0.89 TERT (0.34) KCNH2HSD17B10KDM4EALDH1A1HPGD

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
EP-3459955-B1 NOVEL METHOD AND APPLICATION OF UNSYMMETRICALLY MESO-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT BIOLITEC UNTERNEHMENSBERATUNGS II AG (AT) 2022-11-02 — — EP disclosed
EP-3459955-A1 NOVEL METHOD AND APPLICATION OF UNSYMMETRICALLY MESO-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT biolitec Unternehmensbeteiligungs II AG (AT) 2019-03-27 — — EP disclosed
EP-2350058-B1 NOVEL METHOD AND APPLICATION OF UNSYMMETRICALLY MESO-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT BIOLITEC UNTERNEHMENSBETEILIGUNGS II AG (AT) 2018-10-24 — — EP disclosed
EP-2870159-B1 APPLICATION OF ß-FUNCTIONALIZED DIHYDROXY-CHLORINS FOR PDT BIOLITEC UNTERNEHMENSBETEILIGUNGS II AG (AT) 2017-06-28 — — EP disclosed
CN-103097390-B β functionalization dihydroxy chlorin is used for the application of PDT 拜欧利泰克投资二代公司 2017-03-08 — — CN disclosed
US-9315510-B2 Method and application of unsymmetrically meso-substituted porphyrins and chlorins for PDT BIOLITEC PHARMA MARKETING LTD (MY) 2016-04-19 — — US disclosed
CN-102159569-B The porphyrin replaced for the asymmetric meso of PDT and chlorin and application thereof Beletech Pharmaceutical Market Co.,Ltd. (MY) 2016-02-03 — — CN disclosed
US-9156849-B2 Application of β-functionalized dihydroxy-chlorins for PDT BIOLITEC PHARMA MARKETING LTD (MY) 2015-10-13 — — US disclosed
EP-2870159-A2 APPLICATION OF ß-FUNCTIONALIZED DIHYDROXY-CHLORINS FOR PDT CeramOptec GmbH (DE) 2015-05-13 — — EP disclosed
US-20130041307-A1 APPLICATION OF BETA-FUNCTIONALIZED DIHYDROXY-CHLORINS FOR PDT CERAMOPTEC INDUSTRIES, INC. 2013-02-14 — — US disclosed
WO-2012012809-A2 APPLICATION OF β-FUNCTIONALIZED DIHYDROXY-CHLORINS FOR PDT CERAMOPTEC GMBH (DE) 2012-01-26 — — WO disclosed
US-20110206613-A1 METHOD AND APPLICATION OF UNSYMMETRICALLY meso-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT BIOLITEC UNTERNEHMENSBETEILIGUNGS II AG (AT) 2011-08-25 — — US disclosed
EP-2350058-A2 NOVEL METHOD AND APPLICATION OF UNSYMMETRICALLY MESO-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT CeramOptec GmbH (DE) 2011-08-03 — — EP disclosed
WO-2010033678-A2 NOVEL METHOD AND APPLICATION OF UNSYMMETRICALLY MESO-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT CERAMOPTEC INDUSTRIES, INC. (US) 2010-03-25 — — WO 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-20110206613-A1 METHOD AND APPLICATION OF UNSYMMETRICALLY meso-SUBSTITUTED PORPHYRINS AND CHLORINS FOR PDT PTDSS2, PTDSS1, DLST KCNH2 1786/4885HSD17B10 4149/4885KDM4E 2492/4885
US-20130041307-A1 APPLICATION OF BETA-FUNCTIONALIZED DIHYDROXY-CHLORINS FOR PDT TK1, DHPS, DLD KCNH2 1082/4885HSD17B10 1776/4885KDM4E 1701/4885

“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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