Species

KNApSAcK Entry

Organism name Heliotropium indicum
Genus Heliotropium
Family Boraginaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Heliotropium indicum
Linked NCBI taxonomy ID 248297
Linked level species

Family

Family in NCBI taxonomy Boraginaceae
ID 21571

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (47)

Species Activity
Heliotropium indicum L. Abortifacient
Heliotropium indicum L. Abortifacient
Heliotropium indicum L. Analgesic
Heliotropium indicum L. Analgesic
Heliotropium indicum L. Antiabortive
Heliotropium indicum L. Antiabortive
Heliotropium indicum L. Anticancer
Heliotropium indicum L. Anticancer
Heliotropium indicum L. Antileukemic
Heliotropium indicum L. Antileukemic
Heliotropium indicum L. Antimelanomic
Heliotropium indicum L. Antimelanomic
Heliotropium indicum L. Antispasmodic
Heliotropium indicum L. Antispasmodic
Heliotropium indicum L. Astringent
Heliotropium indicum L. Astringent
Heliotropium indicum L. Carcinogenic
Heliotropium indicum L. Carcinogenic
Heliotropium indicum L. Collyrium
Heliotropium indicum L. Collyrium
Heliotropium indicum L. Depurative
Heliotropium indicum L. Diaphoretic
Heliotropium indicum L. Diaphoretic
Heliotropium indicum L. Diuretic
Heliotropium indicum L. Diuretic
Heliotropium indicum L. Emmenagogue
Heliotropium indicum L. Emmenagogue
Heliotropium indicum L. Emollient
Heliotropium indicum L. Emollient
Heliotropium indicum L. Fungicide
Heliotropium indicum L. Hepatotoxic
Heliotropium indicum L. Hepatotoxic
Heliotropium indicum L. Hypotensive
Heliotropium indicum L. Hypouricemic
Heliotropium indicum L. Hypouricemic
Heliotropium indicum L. Litholytic
Heliotropium indicum L. Pectoral
Heliotropium indicum L. Pectoral
Heliotropium indicum L. Sterilant
Heliotropium indicum L. Stomachic
Heliotropium indicum L. Stomachic
Heliotropium indicum L. Tonic
Heliotropium indicum L. toxic
Heliotropium indicum L. Uterotonic
Heliotropium indicum L. Uterotonic
Heliotropium indicum L. Vulnerary
Heliotropium indicum L. Vulnerary

Metabolite list (8)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00023774 External link 512 Fucostanol
/ Stigmasterol
/ Dihydro-beta-sitosterol
/ (24S)24-Ethylcholestain-3beta-ol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00007271 External link 512 24-Methylenecholesterol
/ 24-Methylene cholesterol
/ 24-Methylcholesta-5,24(28)-dien-3beta-ol
CHEMBL477971
C002537
No. 53 No. 11
C00003647 External link 512 Campesterol
/ 24alpha-Methylcholesterol
/ (24R)24-Methylcholest-5-en-3beta-ol
CHEMBL520535
CHEMBL485421
CHEMBL1836653
C021273
No. 53 No. 11
C00002090 External link 512 Heliotrine
CHEMBL1474445
CHEMBL1978598
CHEMBL2165593
C010178
6 / 3 / 4 No. 308 No. 2
C00002121 External link 512 Supinine
No. 308 No. 2
C00002091 External link 512 Indicine
CHEMBL445876
CHEMBL471483
CHEMBL450265
C018336
No. 308 No. 2
C00026205 External link 512 Indicine N-oxide
CHEMBL352202
CHEMBL512655
CHEMBL516869
C013095
No. 1570

Human Protein / Gene in interactions

22 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002090 C00003672 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002090 C00003672 0 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00002090 C00003672 1 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002090 C00003672 0 / 0
P06746 DNA polymerase beta Enzyme C00003672 C00023774 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00002090 C00003672 0 / 1
P00734 Prothrombin S1A C00003672 4 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
P03372 Estrogen receptor NR3A1 C00003672 1 / 1
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
Q99700 Ataxin-2 Unclassified protein C00002090 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 1 / 1
P11388 DNA topoisomerase 2-alpha Isomerase C00023774 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00023774 0 / 0

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00023774

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#218030 Apparent mineralocorticoid excess; ame P80365
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (12)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)