Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Ingredient: 1Target: 2Links: 2
Arranging relationship network...
Record Fields
Scalar fields from the final ingredient record.
- Ingredient Id
- 15458
- Core Entity Id
- 20349
- Source Entity Count
- 1
- Preferred Name
- Cryptolepine
- Name En
- Pubchem Id
- 82143
- Smiles Canonical
- CN1C2=CC=CC=C2C=C3C1=C4C=CC=CC4=N3
- Molecular Formula
- C16H12N2
- Molecular Weight
- 232.2860
- Inchikey
- KURWKDDWCJELSV-UHFFFAOYSA-N
- Inchi
- InChI=1S/C16H12N2/c1-18-15-9-5-2-6-11(15)10-14-16(18)12-7-3-4-8-13(12)17-14/h2-10H,1H3
- Isomeric Smiles
- CN1C2=CC=CC=C2C=C3C1=C4C=CC=CC4=N3
- Cas Id
- Ob Score
- Mol Logp
- 3.8313
- Num H Donors
- 0
- Num H Acceptors
- 2
- Num Rotatable Bonds
- 0
- Drug Likeness
- 0.4500
- Polar Surface Area
- Molecular Volume
- Alogp
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cryptolepine
Role
preferred
Source
itcmdb_public
Preferred
Yes
Name
Cryptolepine
Role
preferred
Source
HERB_v2
Preferred
Yes
Name
cryptolepine
Role
preferred
Source
TCMBank
Preferred
Yes
Name
480-26-2
Role
alias
Source
HERB_v2
Preferred
No
Name
480-26-2
Role
alias
Source
itcmdb_public
Preferred
No
Name
5-METHYL-5H-INDOLO[3,2-B]QUINOLINE
Role
alias
Source
HERB_v2
Preferred
No
Name
5-METHYL-5H-INDOLO[3,2-B]QUINOLINE
Role
alias
Source
itcmdb_public
Preferred
No
Name
5-methylindolo[3,2-b]quinoline
Role
alias
Source
HERB_v2
Preferred
No
Name
5-methylindolo[3,2-b]quinoline
Role
alias
Source
itcmdb_public
Preferred
No
Name
5H-Quindoline, 5-methyl-
Role
alias
Source
itcmdb_public
Preferred
No
Name
5H-Quindoline, 5-methyl-
Role
alias
Source
HERB_v2
Preferred
No
Name
CCRIS 9019
Role
alias
Source
HERB_v2
Preferred
No
Name
CCRIS 9019
Role
alias
Source
itcmdb_public
Preferred
No
Name
CHEBI:3930
Role
alias
Source
itcmdb_public
Preferred
No
Name
CHEBI:3930
Role
alias
Source
HERB_v2
Preferred
No
Name
Cryptolepine hydrate
Role
alias
Source
itcmdb_public
Preferred
No
Name
Cryptolepine hydrate
Role
alias
Source
HERB_v2
Preferred
No
Name
OF1UIT4RDH
Role
alias
Source
HERB_v2
Preferred
No
Name
OF1UIT4RDH
Role
alias
Source
itcmdb_public
Preferred
No
Name
UNII-OF1UIT4RDH
Role
alias
Source
HERB_v2
Preferred
No
Name
UNII-OF1UIT4RDH
Role
alias
Source
itcmdb_public
Preferred
No
Aliases
Additional names normalized into the restored final schema.
480-26-25-METHYL-5H-INDOLO[3,2-B]QUINOLINE5-methylindolo[3,2-b]quinoline5H-Quindoline, 5-methyl-CCRIS 9019CHEBI:3930Cryptolepine hydrateOF1UIT4RDHUNII-OF1UIT4RDH
Cross References
Trusted external identifiers retained for this final record.
Herb
HBIN021782
Npass
NPC296163
Tcm Id
180055424
Pub Chem
82143
Tcmbank
TCMBANKIN007944
Attributes
Merged source attributes and domain-specific metadata.
In Ch I
InChI=1S/C16H12N2/c1-18-15-9-5-2-6-11(15)10-14-16(18)12-7-3-4-8-13(12)17-14/h2-10H,1H3
Mol Wt
232.286
Smiles
CN1C2=CC=CC=C2C=C3C1=C4C=CC=CC4=N3
Mol Log P
3.831300000000002
In Ch Ikey
KURWKDDWCJELSV-UHFFFAOYSA-N
Num Hdonors
0
Drug Likeness
0.45
Num Hacceptors
2
Isomeric Smiles
CN1C2=CC=CC=C2C=C3C1=C4C=CC=CC4=N3
Canonical Smiles
CN1C2=CC=CC=C2C=C3C1=C4C=CC=CC4=N3
Herb Alias Names
480-26-25-methylindolo[3,2-b]quinoline5H-Quindoline, 5-methyl-5-METHYL-5H-INDOLO[3,2-B]QUINOLINECCRIS 9019CHEBI:3930OF1UIT4RDHCryptolepine hydrateUNII-OF1UIT4RDH
Molecular Weight
232.28 g/mol
Molecular Formula
C16H12N2
Molecular Formula
C16H12N2
Num Rotatable Bonds
0