Isocryptolepine

Isocryptolepine

SCHEMBL9390637

Cn1cc2c3ccccc3nc-2c2ccccc21

nearest known ligand 0.54

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.54
▸ TSHR P16473 3/20 0.54
▸ LMNA P02545 3/20 0.54
▸ KDM4E B2RXH2 2/20 0.54
▸ NPC1 O15118 2/20 0.54
▸ HPGD P15428 2/20 0.54
▸ RAB9A P51151 2/20 0.54
▸ SMN1; SMN2 Q16637 2/20 0.54
▸ HSD17B10 Q99714 2/20 0.54
▸ MAPT P10636 1/20 0.54
▸ HTT P42858 1/20 0.54
▸ CDK5 Q00535 2/20 0.50
▸ CDK5R1 Q15078 2/20 0.50
▸ CYP1A2 P05177 7/20 0.49
▸ CYP3A4 P08684 6/20 0.49
▸ USP2 O75604 6/20 0.49
▸ MEN1 O00255 5/20 0.49
▸ KMT2A Q03164 5/20 0.49
▸ CASP1 P29466 4/20 0.49
▸ CASP7 P55210 4/20 0.49

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
Isocryptolepine SCHEMBL29349681 1.00 ALDH1A1 (0.54) ALDH1A1TSHRLMNAKDM4ENPC1
SCHEMBL7817360 0.79 CYP3A4 (0.62) ALDH1A1TSHRLMNAKDM4ENPC1
SCHEMBL21660484 0.78 KDM4E (0.55) TSHRKDM4EHPGDHTTCYP1A2
SCHEMBL7815125 0.75 RAB9A (0.67) ALDH1A1TSHRLMNAKDM4ENPC1
SCHEMBL21660696 0.74 KDM4E (0.42) ALDH1A1LMNAKDM4EHPGDHSD17B10
SCHEMBL17179429 0.72 NPC1 (0.54) ALDH1A1TSHRLMNAKDM4ENPC1
SCHEMBL21660634 0.72 KDM4E (0.43) ALDH1A1TSHRLMNAKDM4EHPGD
SCHEMBL21660737 0.72 KDM4E (0.47) ALDH1A1TSHRLMNAKDM4EHPGD
SCHEMBL21660523 0.72 MEN1 (0.42) ALDH1A1KDM4EHPGDHSD17B10MAPT
SCHEMBL1310255 0.72 IMPDH2 (0.64) ALDH1A1TSHRLMNAKDM4ENPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2015147666-A1 N-GUANYL DERIVATIVES OF 9-AMINO-5.1 1 -DIMETHYL-5H-INDOLO[2,3-B]QUINOLINE HAVING CYTOTOXIC ACTIVITY INSTYTUT FARMACEUTYCZNY (PL) 2015-10-01 — — WO disclosed
CN-102924448-A Alkaloid cryptolepine analogue quindoline acid compound and preparation method UNIV BOHAI 2013-02-13 — — CN disclosed
WO-1994018203-A1 ALKALOID COMPOUNDS EXTRACTED FROM CRYPTOLEPIS SANQUINOLENTA AND USES THEREOF HEALTHSEARCH, INC. (US) 1994-08-18 — — WO disclosed
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